المؤلفون: Nohemí Carreras-Villaseñor, José B. Rodríguez-Haas, Luis A. Martínez-Rodríguez, Alan J. Pérez-Lira, Enrique Ibarra-Laclette, Emanuel Villafán, Ana P. Castillo-Díaz, Luis A. Ibarra-Juárez, Edgar D. Carrillo-Hernández, Diana Sánchez-Rangel

المصدر: Journal of Fungi; Volume 8; Issue 3; Pages: 231

مصطلحات موضوعية: ambrosia fungi, symbiote fungi, Fusarium, Xylosandrus morigerus, phytopathogen

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.3390/jof8030231Test

الإتاحة: https://doi.org/10.3390/jof8030231Test

المؤلفون: Zytynska, Sharon E., Tighiouart, Karim, Frago, Enric

المصدر: Molecular Ecology

مصطلحات موضوعية: H10 - Ravageurs des plantes, L50 - Physiologie et biochimie animales, Symbiote, Insecte suceur, Aphidoidea, Heteroptera, Analyse coût avantage, Physiologie animale, Interactions biologiques, http://aims.fao.org/aos/agrovoc/c_7562Test, http://aims.fao.org/aos/agrovoc/c_7491Test, http://aims.fao.org/aos/agrovoc/c_30757Test, http://aims.fao.org/aos/agrovoc/c_3585Test, http://aims.fao.org/aos/agrovoc/c_1919Test, http://aims.fao.org/aos/agrovoc/c_25187Test, http://aims.fao.org/aos/agrovoc/c_49896Test

وصف الملف: text

العلاقة: http://agritrop.cirad.fr/598628Test/; Benefits and costs of hosting facultative symbionts in plant-sucking insects: A meta-analysis. Zytynska Sharon E., Tighiouart Karim, Frago Enric. 2021. Molecular Ecology, 30 (11) : 2483-2494.https://doi.org/10.1111/mec.15897Test; http://agritrop.cirad.fr/598628/1/fragomec.15897.pdfTest

الإتاحة: https://doi.org/10.1111/mec.15897Test
http://agritrop.cirad.fr/598628Test/
http://agritrop.cirad.fr/598628/1/fragomec.15897.pdfTest

المؤلفون: Abir Hafsi, Hélène Delatte

المصدر: Biological Invasions

مصطلحات موضوعية: Symbiote, Ecology, Infestation, Tephritidae, H10 - Ravageurs des plantes, C30 - Documentation et information, Enterobacteriaceae, Dynamique des populations, Facilitation des échanges, Ecology, Evolution, Behavior and Systematics, Espèce envahissante

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4568770a38dbf2a179490ace88ae2033Test
https://doi.org/10.1007/s10530-022-02960-xTest

المؤلفون: Minard, Guillaume

المساهمون: Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Ecole Nationale Vétérinaire de Lyon (ENVL)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), PNR EST

المصدر: ISSN: 2264-7597 ; EISSN: 2495-344X ; Les cahiers de la Recherche : Santé, Environnement, Travail.

مصطلحات موضوعية: microorganisme, eau, moustique, lutte contre moustique, Aedes albopictus, insecticide, virus Chikungunya, dengue, kairomone, composé organique volatil, Apicomplexa, parasite, Gregarina, oocyte, symbiote, [SDV.EE.SANT]Life Sciences [q-bio]/Ecology, environment/Health, [SDE.ES]Environmental Sciences/Environment and Society, [SDE.MCG]Environmental Sciences/Global Changes

العلاقة: anses-03108786; https://anses.hal.science/anses-03108786Test; https://anses.hal.science/anses-03108786/documentTest; https://anses.hal.science/anses-03108786/file/2020_CDLR_minard_nouveau_candidat_pour_lutter_contre_moustique_tigre.pdfTest

الإتاحة: https://anses.hal.science/anses-03108786Test
https://anses.hal.science/anses-03108786/documentTest
https://anses.hal.science/anses-03108786/file/2020_CDLR_minard_nouveau_candidat_pour_lutter_contre_moustique_tigre.pdfTest

المؤلفون: Cano-Calle, Daniela

المساهمون: Arango Isaza, Rafael Eduardo, Moreno Herrera, Claudia Ximena, Saldamando Benjumea, Clara Inés, BIOTECNOLOGÍA VEGETAL UNALMED - CIB y MiCROBIODIVERSIDAD Y BIOPROSPECCIÓN

مصطلحات موضوعية: Biotecnología Molecular y Agrícola, Wolbachia, PCR, 16S rDNA, avocado, symbiote, DNAr 16S, aguacate, simbionte

وصف الملف: application/pdf

العلاقة: Altschul, S. F., Madden, T. L., Schäffer, A. A., Zhang, J., Zhang, Z., Miller, W., & Lipman, D. J. (1997). Gapped BLAST and PSI-BLAST : a new generation of protein database search programs. Oxford University Press, 25(17), 3389–3402.; Ambika, S., & Rajagopal, R. (2018). Lumen anatomy and localization of Wolbachia sp. in the thrips, Plicothrips apicalis (Bagnall). Current Science, 115(7), 1297–1304. https://doi.org/doi:10.18520/cs/v115/i7/1297-1304Test; Amórtegui Ferro, I. (2001). El cultivo del aguacate: Módulo Educativo para el Desarrollo Tecnológico de la comunidad Rural.; An, R., Sreevatsan, S., & Grewal, P. S. (2008). Moraxella osloensis Gene Expression in the Slug Host Deroceras reticulatum. BMC Microbiology, 8(19), 1–11. https://doi.org/10.1186/1471-2180-8-19Test; Anacafe. (2004). Cultivo de aguacate. Asociacion Nacional Del Cafe ANACAFE, 1–25.; Apprill, A., Mcnally, S., Parsons, R., & Weber, L. (2015). Minor revision to V4 region SSU rRNA 806R gene primer greatly increases detection of SAR11 bacterioplankton. Aquatic Microbial Ecology, 75(2), 129–137. https://doi.org/10.3354/ame01753Test; Arakaki, N., Miyoshi, T., & Noda, H. (2001). Wolbachia-mediated parthenogenesis in the predatory thrips Franklinothrips vespiformis (Thysanoptera: Insecta). Proceedings of the Royal Society B: Biological Sciences, 268(1471), 1011–1016. https://doi.org/10.1098/rspb.2001.1628Test; Ashworth, V. E., & Clegg, M. T. (2003). Microsatellite Markers in Avocado ( Persea americana Mill .): Genealogical Relationships Among Cultivated Avocado Genotypes. Journal of Heredity, 94(5), 407–415. https://doi.org/10.1093/jhered/esg076Test; Asokan, R., Krishna Kumar, N. K., Kumar, V., & Ranganath, H. R. (2007). Molecular differences in the mitochondrial cytochrome oxidase I (mtCOI) gene and development of a species-specific marker for onion thrips, Thrips tabaci Lindeman, and melon thrips, T. palmi Karny (Thysanoptera: Thripidae), vectors of tospoviruses (Bunyav. Bulletin of Entomological Research, 97, 461–470. https://doi.org/10.1017/S0007485307005147Test; Augustinos, A. A., Kyritsis, G. A., Papadopoulos, N. T., Abd-Alla, A. M. M., Cáceres, C., & Bourtzis, K. (2015). Exploitation of the medfly gut microbiota for the enhancement of sterile insect technique: Use of Enterobacter sp. in larval diet-based probiotic applications. PLoS ONE, 10(9), 1–17. https://doi.org/10.1371/journal.pone.0136459Test; Baldo, L., Dunning H., J. C., Jolley, K. A., Bordenstein, S. R., Biber, S. A., Choudhury, R. R., Werren, J. H. (2006). Multilocus sequence typing system for the endosymbiont Wolbachia pipientis. Applied and Environmental Microbiology, 72(11), 7098–7110. https://doi.org/10.1128/AEM.00731-06Test; Baldo, L., & Werren, J. H. (2007). Revisiting Wolbachia supergroup typing based on WSP: Spurious lineages and discordance with MLST. Current Microbiology, 55(1), 81–87. https://doi.org/10.1007/s00284-007-0055-8Test; Bandi, C., Anderson, T. J. C., Genchi, C., & Blaxter, M. L. (1998). Phylogeny of Wolbachia in filarial nematodes. Proceedings of the Royal Society B: Biological Sciences, 265(1413), 2407–2413. https://doi.org/10.1098/rspb.1998.0591Test; Barak, H., Kumar, P., Zaritsky, A., Mendel, Z., Ment, D., Kushmaro, A., & Ben-dov, E. (2019). Diversity of Bacterial Biota in Capnodis tenebrionis (Coleoptera : Buprestidae) Larvae. Pathogens, 8, 1–9. https://doi.org/10.3390/pathogens8010004Test; Barry, T., Colleran, G., Glennon, F., Dunican, L. K., & Gannon, F. (1991). The 16s / 23s ribosomal spacer region as a target for DNA probes to identify eubacteria service. Genome Res, 1–2. https://doi.org/10.1101/gr.1.2.149-aTest; Bethke, J., Dreistadt, S., & Varela, L. (2014). Tree squirrels - integrated pest management for home gardeners and landscape professionals. Pest Notes. University of California. Agriculture and Natural Resources, 1–8.; Bhandari, B. K., Glazer, I., & Coll, M. (2009). Tropentag 2009 Biophysical and Socio-economic Frame Conditions for the Sustainable Management of Natural Resources , University of Interactions between the omnivorous bug Orius laevigatus and the entomopathogenic nematode Steinernema feltiae , natural ene.; Blumberg, B. J., Short, S. M., & Dimopoulos, G. (2016). Employing the Mosquito Microflora for Disease Control. In Genetic Control of Malaria and Dengue. https://doi.org/10.1016/B978-0-12-800246-9.00015-6Test; Bordenstein, S., & Rosengaus, R. B. (2005). Discovery of a novel Wolbachia supergroup in isoptera. Current Microbiology, 51(6), 393–398. https://doi.org/10.1007/s00284-005-0084-0Test; Braig, H. R., Zhou, W., Dobson, S. L., & Neill, S. L. O. (1998). Cloning and Characterization of a Gene Encoding the Major Surface Protein of the Bacterial Endosymbiont Wolbachia pipientis. Journal of Bacteriology, 180(9), 2373–2378.; Bravo-Pérez, D., Santillán-Galicia, M. T., Johansen-Naime, R. M., González-Hernández, H., Segura-León, O. L., Ochoa-Martínez, D. L., & Guzman-Valencia, S. (2018). Species diversity of thrips (Thysanoptera) in selected avocado orchards from Mexico based on morphology and molecular data. Journal of Integrative Agriculture, 17(11), 2509–2517. https://doi.org/10.1016/S2095-3119Test(18)62044-1; Broderick, N. A., Robinson, C. J., McMahon, M. D., Holt, J., Handelsman, J., & Raffa, K. F. (2009). Contributions of gut bacteria to Bacillus thuringiensis-induced mortality vary across a range of Lepidoptera. BMC Biology, 7(1), 11. https://doi.org/10.1186/1741-7007-7-11Test; Brunner, P. C., Chatzivassiliou, E. K., Katis, N. I., & Frey, J. E. (2004). Host-associated genetic differentiation in Thrips tabaci (Insecta; Thysanoptera), as determined from mtDNA sequence data. Heredity, 93, 364–370. https://doi.org/10.1038/sj.hdy.6800512Test; Brunner, P. C., Fleming, C., & Frey, J. E. (2002). A molecular identification key for economically important thrips species (Thysanoptera: Thripidae) using direct sequencing and a PCR-RFLP-based approach. Agricultural and Forest Entomology, 4(2), 127–136. https://doi.org/10.1046/j.1461-9563.2002.00132.xTest; Brunner, P. C., & Frey, J. E. (2010). Habitat-specific population structure in native western flower thrips frankliniella occidentalis (Insecta, Thysanoptera). Journal of Evolutionary Biology, 23(4), 797–804. https://doi.org/10.1111/j.1420-9101.2010.01946.xTest; Buckman, R. S., Mound, L. A., & Whiting, M. F. (2013). Phylogeny of thrips (Insecta: Thysanoptera) based on five molecular loci. Systematic Entomology, 38, 123–133. https://doi.org/10.1111/j.1365-3113.2012.00650.xTest; Bukin, Y. S., Galachyants, Y. P., Morozov, I. V, Bukin, S. V, Zakharenko, A. S., & Zemskaya, T. I. (2019). Data Descriptor: The effect of 16 S rRNA region choice on bacterial community metabarcoding results. Scientific Data, 6, 190007. https://doi.org/10.1038/sdata.2019.7Test; Bustillo, A. E. (2009). Evaluación de insecticidas quuímicos y biológicos para controlar Frankliniella occidentalis (Thysanoptera: Thripidae) en cultivos de espárragos. Revista Colombiana de Entomologia, 35(1), 12–17.; CABI. (2015). Frankliniella occidentalis (western flower thrips). Retrieved from http://www.cabi.org/isc/datasheet/24426Test; Calixto, C. L. (2005). Sección Morfologica, Comportamiento, Ecología, Evolución y Sistemática Trips del Suborden Terebrantia (Insecta: Thysanoptera) en la Sabana de Bogotá) (pp. 207–213). pp. 207–213.; Camarinha-Silva, A., Jáuregui, R., Chaves-Moreno, D., Oxley, A. P. A., Schaumburg, F., Becker, K., … Pieper, D. H. (2014). Comparing the anterior nare bacterial community of two discrete human populations using Illumina amplicon sequencing. Environmental Microbiology, 16(9), 2939–2952. https://doi.org/10.1111/1462-2920.12362Test; Cambero-campos, J., Johansen-Naime, R., García-Martínez, O., Cantu-Sifuentes, M., Cerna-Chavez, E., & Renata-Salazar, A. (2011). Especies Depredadoras de Trips (Thysanoptera) Asociadas a Huertas de Aguacate en Nayarit, México. Acta Zoológica Mexicana, 27(1), 115–121. Retrieved from http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S0065-17372011000100009&lng=es&nrm=isoTest; Cambero, O., Johansen, R., Retana, A., García, O., Cantú, M., & Carvajal, C. (2010). Thrips (Thysanoptera) del aguacate (Persea americana) en Nayarit, México. Revista Colombiana de Entomologia, 36(1), 47–51. Retrieved from http://www.scielo.org.co/pdf/rcen/v36n1/v36n1a09.pdfTest; Cameron, S. L. (2014). Insect mitochondrial genomics: implications for evolution and phylogeny. Annu Rev Entomol, 59(October 2013), 95–117. https://doi.org/10.1146/annurev-ento-011613-162007Test; Campos Rojas, E., Terrazas, T., & López-Mata, L. (2007). Persea ( avocados ) phylogenetic analysis based on morphological characters : hypothesis of species relationships. Genetic Resources and Crop Evolution, 54, 249–258. https://doi.org/10.1007/s10722-005-3808-xTest; Cañas-Gutiérrez, G. P., Alcaraz, L., Hormaza, J. I., Arango-Isaza, R. E., & Saldamando-Benjumea, C. I. (2019). Diversity of avocado (Persea americana mill.) cultivars from antioquia (Northeast Colombia) and comparison with a worldwide germplasm collection. Turkish Journal of Agriculture and Forestry, 43(4), 437–449. https://doi.org/10.3906/tar-1807-25Test; Cañas-Gutiérrez, G. P., Galindo-López, L. F., Arango-Isaza, R., & Saldamando Benjumea, C. I. (2015). Diversidad genética de cultivares de aguacate (Persea americana Mill) en Antioquia, Colombia. Agronomía Mesoamericana, 26(1), 129–143. https://doi.org/10.15517/am.v26i1.16936Test; Cao, Y., Fanning, S., Proos, S., Jordan, K., & Srikumar, S. (2017). A review on the applications of next generation sequencing technologies as applied to food-related microbiome studies. Frontiers in Microbiology, 8(SEP), 1–16. https://doi.org/10.3389/fmicb.2017.01829Test; Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F., Costello, E., … Knight, R. (2010). QIIME allows analysis of high-throughput community sequencing data. Nat Methods, 7(5), 335–336. https://doi.org/10.1038/nmeth.f.303Test; Caragata, E. P., Rocha, M. N., Pereira, T. N., Mansur, S. B., Heverton, L., Id, C. D., & Id, L. A. M. (2019). Pathogen blocking in Wolbachia -infected Aedes aegypti is not affected by Zika and dengue virus co-infection. PLoS Neglected Tropical Diseases, 13(5), e0007443. https://doi.org/https://doi.org/10.1371/journal.pntd.0007443Test; Cardenas, E., & Corredor, D. (1993). Especies De Trips ( Thysanoptera : Thripidae ) Mas Comunes En Invernaderos De Flores De La Sabana De Bogota. Agronomía Colombiana, 10(2), 132–143.; Carvajal, T. M., Hashimoto, K., Harnandika, R. K., Amalin, D. M., & Watanabe, K. (2019). Detection of Wolbachia in field‑collected Aedes aegypti mosquitoes in metropolitan Manila, Philippines. Parasites & Vectors, 12, 361. https://doi.org/10.1186/s13071-019-3629-yTest; Casiraghi, M., Bordenstein, S. R., Baldo, L., Lo, N., Beninati, T., Wernegreen, J. J., … Bandi, C. (2005). Phylogeny of Wolbachia pipientis based on gltA, groEL and ftsZ gene sequences: Clustering of arthropod and nematode symbionts in the F supergroup, and evidence for further diversity in the Wolbachia tree. Microbiology, 151(12), 4015–4022. https://doi.org/10.1099/mic.0.28313-0Test; Casiraghi, Maurizio, Bain, O., Guerrero, R., Martin, C., Pocacqua, V., Gardner, S. L., … Bandi, C. (2004). Mapping the presence of Wolbachia pipientis on the phylogeny of filarial nematodes: Evidence for symbiont loss during evolution. International Journal for Parasitology, 34(2), 191–203. https://doi.org/10.1016/j.ijpara.2003.10.004Test; Castañeda-Monsalve, V. A., Junca, H., García-Bonilla, E., Montoya-Campuzano, O. I., & Moreno-Herrera, C. X. (2019). Characterization of the gastrointestinal bacterial microbiome of farmed juvenile and adult white Cachama (Piaractus brachypomus). Aquaculture, 512, 734325. https://doi.org/10.1016/j.aquaculture.2019.734325Test; Cawoy, H., Bettiol, W., Fickers, P., & Ongena, M. (2011). Bacillus-Based Biological Control of Plant Diseases. In M. Stoytcheva (Ed.), PESTICIDES IN THE MODERN WORLD – PESTS CONTROL AND PESTICIDES EXPOSURE (pp. 273–302). https://doi.org/10.5772/948Test; Chakravorty, S., Helb, D., Burday, M., Connell, N., & Alland, D. (2007). A detailed analysis of 16S ribosomal RNA gene segments for the diagnosis of pathogenic bacteria. J Microbiol Methods, 69(2), 330–339. https://doi.org/10.1016/j.mimet.2007.02.005.ATest; Champoux, J. J. (2001). DNA TOPOISOMERASES: Structure, Function, and Mechanism. Annu. Rev. Biochem, 70, 369–413. https://doi.org/10.1146/annurev.biochem.70.1.369Test; Chanbusarakum, L., & Ullman, D. (2008). Characterization of bacterial symbionts in Frankliniella occidentalis (Pergande), Western flower thrips. Journal of Invertebrate Pathology, 99(3), 318–325. https://doi.org/10.1016/j.jip.2008.09.001Test; Chao, A. (1984). Nonparametric Estimation of the Number of Classes in a Population. Scandinavian Journal of Statistics, 11(4), 265–270. Retrieved from http://www.jstor.org/stable/4615964Test; Chaudhary, N., Sharma, A. K., Agarwal, P., Gupta, A., & Sharma, V. (2015). 16S Classifier: A Tool for Fast and Accurate Taxonomic Classification of 16S rRNA Hypervariable Regions in Metagenomic Datasets. PLoS ONE, 10(1), e0116106. https://doi.org/10.1371/journal.pone.0116106Test; Choudhary, D. K., & Johri, B. N. (2009). Interactions of Bacillus spp. and plants - With special reference to induced systemic resistance (ISR). Microbiological Research, 164(5), 493–513. https://doi.org/10.1016/j.micres.2008.08.007Test; Chua, K., Song, S., Yong, H., See-too, W.-S., Yin, W., & Chan, K.-G. (2018). Microbial Community Composition Reveals Spatial Variation and Distinctive Core Microbiome of the Weaver Ant Oecophylla smaragdina in Malaysia. Scientific Reports, 8, 1–11. https://doi.org/10.1038/s41598-018-29159-2Test; Cloyd, R. A. (2010). Western Flower Thrips Management on Greenhouse-Grown Crops.; Cloyd, R. A., & Sadof, C. S. (2011). Western Flower Thrips. Landscape and Ornamentals.; Cocolin, L., Mataragas, M., Bourdichon, F., Doulgeraki, A., Pilet, M. F., Jagadeesan, B., … Phister, T. (2018). Next generation microbiological risk assessment meta-omics: The next need for integration. International Journal of Food Microbiology, 287(March 2017), 10–17. https://doi.org/10.1016/j.ijfoodmicro.2017.11.008Test; Cole, J. R., Wang, Q., Cardenas, E., Fish, J., Chai, B., Farris, R. J., … Tiedje, J. M. (2009). The Ribosomal Database Project: Improved alignments and new tools for rRNA analysis. Nucleic Acids Research, 37, 141–145. https://doi.org/10.1093/nar/gkn879Test; Coulibaly, Y. I., Dembele, B., Diallo, A. A., Lipner, E. M., Doumbia, S. S., Coulibaly, S. Y., … Klion, A. D. (2009). A randomized trial of doxycycline for mansonella perstans infection. New England Journal of Medicine, 361(15), 1448–1458. https://doi.org/10.1056/NEJMoa0900863Test; Coutinho-Abreu, I. V., Zhu, K. Y., & Ramalho-Ortigao, M. (2011). Transgenesis and paratransgenesis to control insect-borne disease: Current status and future challenges. Parasitology International, 59(1), 1–8. https://doi.org/10.1016/j.parint.2009.10.002.TransgenesisTest; Cox, J., Ballweg, R., Taft, D. H., Velayutham, P., Haslam, D., & Porollo, A. (2017). A fast and robust protocol for metataxonomic analysis using RNAseq data. Microbiome, 5(7), 1–13. https://doi.org/10.1186/s40168-016-0219-5Test; Crane, J. H., Balerdi, C. F., & Manguire, I. (2013). Avocado Growing in the Florida Home Landscape. Institute of Food and Agricultural Sciences, 1–6.; Czarnetzki, A. B., & Tebbe, C. C. (2004). Detection and phylogenetic analysis of Wolbachia in Collembola. Environmental Microbiology, 6(1), 35–44. https://doi.org/10.1046/j.1462-2920.2003.00537.xTest; D’Argenio, V., & Salvatore, F. (2015). The role of the gut microbiome in the healthy adult status. Clinica Chimica Acta, 451, 97–102. https://doi.org/10.1016/j.cca.2015.01.003Test; De Grazia, A., Marullo, R., & Moritz, G. (2016). Molecular diagnosis of native and quarantine pest thrips of southern European citrus orchards. Bulletin of Insectology, 69(1), 1–6.; De Vries, E., Breeuwer, J., Jacobs, G., & Mollema, C. (2001). The association of Western flower thrips, Frankliniella occidentalis, with a near Erwinia species gut bacteria: transient or permanent? Journal of Invertebrate Pathology, 77(2), 120–128. https://doi.org/10.1006/jipa.2001.5009Test; De Vries, E., Jacobs, G., & Breeuwer, J. (2001). Growth and transmission of gut bacteria in the western flower thrips, Frankliniella occidentalis. In Symbiosis of thrips and gut bacteria. Retrieved from http://dare.uva.nl/record/1/317961Test; De Vries, E.J., Van Der Wurff, A. G., Jacobs, G., & Breeuwer, J. . (2008). Onion thrips , Thrips tabaci , have gut bacteria that are closely related to the symbionts of the western flower thrips , Frankliniella occidentalis. Insect Science, 8, 11. Retrieved from insectscience.org/8.23; De Vries, Egbert Jacob. (2010). Symbiosis Symbiosis of of thrips and gut bacteria (Universiteit van Amsterdam). Retrieved from http://dare.uva.nl/document/2/72571Test; De Vries, Egbert, Van de Wetering, F., Van der Hoek, M., Jacobs, G., & Breeuwer, J. (2012). Symbiotic bacteria (Erwinia sp.) in the gut of Frankliniella occidentalis (Thysanoptera: Thripidae) do not affect its ability to transmit tospovirus. European Journal of Entomology, 109(2), 261–266.; De Vries, Jacobs, G., Sabelis, M., Menken, S., & Breeuwer, J. (2004). Diet-dependent effects of gut bacteria on their insect host : the symbiosis of Erwinia sp . and western flower thrips. Proc. R. Soc. Lond. B, 271, 2171–2178. https://doi.org/10.1098/rspb.2004.2817Test; Department of Agriculture forestry and Fisharies. (2012). Avocado (pp. 1–73). pp. 1–73.; Diaz-Grisales, V., Caicedo-Vallejo, M., & Carabalí-Muñoz, A. (2017). CICLO DE VIDA Y DESCRIPCIÓN MORFOLÓGICA DE HEILIPUS LAURI BOHEMAN ( COLEOPTERA : CURCULIONIDAE ) EN COLOMBIA LIFE CYCLE AND MORPHOLOGICAL DESCRIPTION OF HEILIPUS LAURI BOHEMAN ( COLEOPTERA : CURCULIONIDAE ) IN COLOMBIA. Acta Zoológica Mexicana, 33(2), 231–242.; Dickey, A. M., Trease, A. J., Jara-Cavieres, A., Kumar, V., Christenson, M. K., Potluri, L. P., … Osborne, L. S. (2014). Estimating bacterial diversity in Scirtothrips dorsalis (Thysanoptera: Thripidae) via next generation sequencing. Florida Entomologist, 97(2), 362–366. https://doi.org/10.1896/054.097.0204Test; Dillon, R. J., & Dillon, V. M. (2004). THE GUT BACTERIA OF INSECTS: Nonpathogenic Interactions. Annual Review of Entomology, 49(1), 71–92. https://doi.org/10.1146/annurev.ento.49.061802.123416Test; Ding, T., Chi, H., Gökçe, A., Gao, Y., & Zhang, B. (2018). Demographic analysis of arrhenotokous parthenogenesis and bisexual reproduction of Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae). Scientific Reports, 8, 3346. https://doi.org/10.1038/s41598-018-21689-zTest; DISPLAYR. (n.d.). Retrieved April 15, 2020, from https://www.displayr.comTest/; Douglas, A. E. (2009). The microbial dimension in insect nutritional ecology. Functional Ecology, 23(1), 38–47. https://doi.org/10.1111/j.1365-2435.2008.01442.xTest; Douglas, Angela E. (2015). Multiorganismal Insects: Diversity and Function of Resident Microorganisms. Annual Review of Entomology, 60(1), 17–34. https://doi.org/10.1146/annurev-ento-010814-020822Test; Dreistadt, S. H., Phillips, P. A., & O’Donnell, C. A. (2007). Thrips. Integrated Pest Management for Home Gardeners and Landscape Professionals. Pest Notes. University of California. Agriculture and Natural Resources, (March), 1–7. Retrieved from http://www.ipm.ucdavis.edu/PDF/PESTNOTES/pncoyote.pdfTest; Driutti, A. (1999). Control biológico natural de trips, Thrips tabaci Lindeman 1888 (Thysanoptera: Thripidae) por sírfidos predadores en cultivo de cebolla (Allium cepa L.) por el cultivo de borduras y/o entrelineas.1.; Duron, O., & Hurst, G. D. (2013). Arthropods and inherited bacteria: from counting the symbionts to understanding how symbionts count. BMC Biology, 11, 45. https://doi.org/10.1186/1741-7007-11-45Test; Dutta, B., Barman, A. K., Srinivasan, R., Avci, U., Ullman, D., Langston Jr., D. B., & Gitaitis, R. (2014). Transmission of Pantoea ananatis and Pantoea agglomerans causal agents of center rot of onion (Allium cepa L.) by onion thrips (Thrips tabaci Lindeman). Phytopathology, (17), 140218150216004. https://doi.org/10.1094/PHYTO-07-13-0199-RTest; Echeverri Florez, Fernando Loaiza Marín, C. E., & Cano Ortiz, M. del P. (2004). Reconocimiento e identificación de trips fitófagos (Thysanoptera: Thripidae) y depredadores (Thysanoptera: Phlaeothripidae) asociados a cultivos comerciales de aguacate Persea spp. en los departamentos de Caldas y Risaralda (Colombia). Revista Facultad Nacional de Agronomía Medellín, 57(1), 2178–2189. Retrieved from http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0304-28472004000100003&lng=en&nrm=isoTest; Edgar, R. C. (2004). MUSCLE: A multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics, 5, 113. https://doi.org/10.1186/1471-2105-5-113Test; Eleftherianos, I., Yadav, S., Kenney, E., Cooper, D., Ozakman, Y., & Patrnogic, J. (2017). Role of Endosymbionts in Insect-Parasitic Nematode Interactions. Trends in Parasitology, xx, 1–15. https://doi.org/10.1016/j.pt.2017.10.004Test; Engel, P., & Moran, N. A. (2013). The gut microbiota of insects - diversity in structure and function. FEMS Microbiology Reviews, Vol. 37. https://doi.org/10.1111/1574-6976.12025Test; Espejo, R. T., Feijóo, C. G., Romero, J., & Vásquez, M. (1998). PACE analysis of the heteroduplexes formed between PCR-amplified 16S rRNA genes: Estimation of sequence similarity and rDNA complexity. Microbiology, 144(6), 1611–1617. https://doi.org/10.1099/00221287-144-6-1611Test; Excoffier, L., Laval, G., & Schneider, S. (2005). Arlequin (version 3.0): An integrated software package for population genetics data analysis. Evolutionary Bioinformatics, 1, 47–50. https://doi.org/10.1111/j.1755-0998.2010.02847.xTest; Facey, P. D., Méric, G., Hitchings, M. D., Pachebat, J. A., Hegarty, M. J., Chen, X., … Del Sol, R. (2015). Draft genomes, phylogenetic reconstruction, and comparative genomics of two novel cohabiting bacterial symbionts isolated from Frankliniella occidentalis. Genome Biology and Evolution, 7(8), 2188–2202. https://doi.org/10.1093/gbe/evv136Test; FAO. (2018). Database FAOSTAT. Retrieved February 3, 2019, from http://www.fao.org/faostat/es/#data/QCTest; Folmer, O., Black, M., Hoeh, W., Lutz, R., & Vrijenhoek, R. (1994). DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3(5), 294–299. https://doi.org/10.1371/journal.pone.0013102Test; Frey, J. E., & Frey, B. (2004). Origin of intra-individual variation in PCR-amplified mitochondrial cytochrome oxidade I of Thrips tabaci (Thysanoptera: Thripidae): Mitochondrial heteroplasmy or nuclear integration? Hereditas, 140(2), 92–98. https://doi.org/10.1111/j.1601-5223.2004.01748.xTest; Gallego, C. M., Mora, C. M., Guarín, J. H., & Madrigal, A. (2002). Evaluación en campo del potencial de hongos entomopatógenos controladores de Thrips palme KARNY (Thysanoptera: Thripidae).; Gawande, S. J., Anandhan, S., Ingle, A., Roylawar, P., Khandagale, K., Gawai, T., … Singh, M. (2019). Microbiome profiling of the onion thrips, Thrips tabaci Lindeman (Thysanoptera: Thripidae ). PLoS ONE, 14(9), e0223281. https://doi.org/https://doi.org/10.1371Test/ journal.pone.0223281; Genkai-Kato, M., & Yamamura, N. (1999). Evolution of mutualistic symbiosis without vertical transmission. Theoretical Population Biology, 55(3), 309–323. https://doi.org/10.1006/tpbi.1998.1407Test; Gill, H. K., Garg, H., Gill, A. K., Gillett-kaufman, J. L., & Nault, B. A. (2015). Onion Thrips (Thysanoptera: Thripidae) Biology, Ecology, and Management in Onion Production Systems. Journal of Integrated Pest Management, 6(1), 6. https://doi.org/10.1093/jipm/pmv006Test; Goldenberger, D., Perschil, I., Ritzler, M., & Altwegg, M. (1995). A Simple “Universal” DNA Extraction Procedure Using SDS and Proteinase K is Compatible with direct PCR amplification. PCR Methods and Applications, 4(6), 368–370. https://doi.org/10.1101/gr.4.6.368Test; Gomez, A. M., Yannarell, A. C., Sims, G. K., Cadavid-Restrepo, G., & Moreno Herrera, C. X. (2011). Characterization of bacterial diversity at different depths in the Moravia Hill landfill site at Medellín, Colombia. Soil Biology and Biochemistry, 43, 1275–1284. https://doi.org/10.1016/j.soilbio.2011.02.018Test; González-Herrera, A. (2003). Artropodos Asociados Al Cultivo Del Aguacate ( Per- Sea Americana Mill .) En Costa Rica. In Proceedings V World Avocado Congress.; Gorham, C. H., Fang, Q. Q., & Durden, L. A. (2003). Wolbachia Endosymbionts in Fleas (Siphonaptera). Journal of Parasitology, 89(2), 283–289. https://doi.org/10.1645/0022-3395Test(2003)089[0283:weifs]2.0.co;2; Granadillo, J. (2014). Integrated Pest Management of Western Flower Thrips. 32.; Granados, W., & Valencia, J. (2018). Cadena de aguacate. Indicadores e Instrumentos. Retrieved from https://sioc.minagricultura.gov.co/Aguacate/Documentos/2018-08-30Test Cifras Sectoriales.pdf; Gürsoy, O., & Can, M. (2019). Hypervariable Regions in 16S rRNA Genes for the Taxonomic Classification. Southeast Europe Journal of Soft Computing Vol.8, 8(1), 23–26. https://doi.org/http://dx.doi.org/10.21533/scjournal.v8i1.171Test; Gürtler, V., & Stanisich, V. (1996). New approaches to typing and identification of bacteria using the 16s-23s rDNA spacer region. Microbiology, 142, 3–16.; Hajibabaei, M., Singer, G. A. C., Hebert, P. D. N., & Hickey, D. A. (2007). DNA barcoding: how it complements taxonomy, molecular phylogenetics and population genetics. Trends in Genetics, 23(4), 167–172. https://doi.org/10.1016/j.tig.2007.02.001Test; Hammer, Ø., Harper, D. A. T., & Ryan, P. D. (2001). PAST : Paleontological Statistics Software Package for Education and Data Analysis PAST : PALEONTOLOGICAL STATISTICS SOFTWARE PACKAGE FOR EDUCATION AND DATA ANALYSIS Even a cursory glance at the recent paleontological literature should convince anyone tha. Palaeontologia Electronica, 4(1), 1–9.; Handelsman, J. (2004). Metagenomics : Application of Genomics to Uncultured Microorganisms. Microbiology and Molecular Biology Reviews, 68(4), 669–685. https://doi.org/10.1128/MBR.68.4.669Test; Hansen, E. A., Funderburk, J. O. E. E., Reitz, S. R., Ramachandran, S., Eger, J. O. E. E., & Mcauslane, H. (2003). Within-Plant Distribution of Frankliniella species ( Thysanoptera : Thripidae ) and Orius insidiosus ( Heteroptera : Anthocoridae ) in Field Pepper.; Hara, A., Mau, R., Heu, R., Jacobsen, C., & Niino-DuPonte, R. (2002). Damage to Banana and Ornamentals in Hawaii. Tropical Agriculture, (June), 8–11.; Hebert, P. D. N., Cywinska, A., Ball, S. L., & deWaard, J. R. (2003). Biological identifications through DNA barcodes. Proceedings. Biological Sciences / The Royal Society, 270(1512), 313–321. https://doi.org/10.1098/rspb.2002.2218Test; Hebert, P. D. N., Ratnasingham, S., & Jeremy, R. (2003). Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species. Proc. R. Soc. Lond. B, 270, S96–S99. https://doi.org/10.1098/rsbl.2003.0025Test; Hebert, P. D. N., Stoeckle, M. Y., Zemlak, T. S., & Francis, C. M. (2004). Identification of Birds through DNA Barcodes. PLoS Biology, 2(10), e312. https://doi.org/10.1371/journal.pbio.0020312Test; Hedges, L. M., Brownlie, J. C., O’Neill, S. L., & Johnson, K. N. (2008). Wolbachia and virus protection in insects. Science, 322(5902), 702. https://doi.org/10.1126/science.1162418Test; Hilgenboecker, K., Hammerstein, P., Schlattmann, P., Telschow, A., & Werren, J. H. (2008). How many species are infected with Wolbachia?- a statistical analysis of current data. FEMS Microbiology Letters, 281, 215–220. https://doi.org/10.1111/j.1574-6968.2008.01110.xTest; Hoddle, M. (2013). Applied Biological Control Research_ Biological Control of Western Flower Thrips. Retrieved from University of California website: http://biocontrol.ucr.edu/wft.htmlTest; Hoddle, M., & Mound, L. (2003). The Genus Scirtothrips In Australia (Insecta, Thysanoptera, Thripidae). Zootaxa, (268), 1–40. https://doi.org/10.11646/zootaxa.268.1.1Test; Hoy, M. A. (1994). Insect Molecular Genetics (Academic P).; Huang, S., & Zhang, H. (2013). The Impact of Environmental Heterogeneity and Life Stage on the Hindgut Microbiota of Holotrichia parallela Larvae (Coleoptera: Scarabaeidae ). PLoS ONE, 8(2), e57169. https://doi.org/10.1371/journal.pone.0057169Test; Iftikhar, R., Ashfaq, M., Rasool, A., & Hebert, P. D. N. (2016). DNA Barcode Analysis of Thrips (Thysanoptera) Diversity in Pakistan Reveals Cryptic Species Complexes. PLoS ONE, 11(1), e0146014. https://doi.org/10.1371/journal.pone.0146014Test; Instituto Colombiano de Agricultura (ICA). (2012). Manejo fitosanitario del cultivo del aguacate (Persea americana Mill.). Medidas para la temporada invernal. Línea Agrícola, 1, 73.; Ish-Am, G. (2004). Avocado pollination basics, a short review. 2° Seminario Internacional de Paltos, 1–10.; Ish-Am, Gad, & Eisikowitch, D. (1993). The behaviour of honey bees (Apis mellifera) visiting avocado (Persea americana) flowers and their contribution to its pollination. Journal of Apicultural Research, 32(3–4), 175–186. https://doi.org/10.1080/00218839.1993.11101303Test; Izzo, T., Pinent, S., & Mound, L. A. (2002). AULACOTHRIPS DICTYOTUS ( HETEROTHRIPIDAE ), THE FIRST ECTOPARASITIC THRIPS ( THYSANOPTERA ). Scientific Notes, pp. 281–283.; Jacob, T. K., D’silva, S., Senthil Kumar, C. M., Devasahayam, S., Rajalakshmi, V., Sujeesh, E. S., … Abraham, S. (2014). Single strain infection of adult and larval cardamom thrips (Sciothrips cardamomi) by Wolbachia subgroup Con belonging to supergroup B in India. Invertebrate Reproduction and Development, 59(1), 1–8. https://doi.org/10.1080/07924259.2014.970237Test; Janssen, P. H. (2006). Identifying the Dominant Soil Bacterial Taxa in Libraries of 16S rRNA and 16S rRNA Genes. Applied and Environmental Microbiology, 72(3), 1719–1728. https://doi.org/10.1128/AEM.72.3.1719Test; Jardón Barbolla, L., Alavez Gómez, V., Méndez, V., Gaona, A., Damián Domínguez, M., Piñero, D., … Wegier, A. L. (2013). Análisis para la determinación de los centros de origen, domesticación y diversidad genética del género Persea y la especie Persea americana (aguacate).; Jeffries, C. L., & Walker, T. (2016). Wolbachia Biocontrol Strategies for Arboviral Diseases and the Potential Influence of Resident Wolbachia Strains in Mosquitoes. Current Tropical Medicine Reports, 3(1), 20–25. https://doi.org/10.1007/s40475-016-0066-2Test; Jones, A., Mason, C., Felton, G., & Hoover, K. (2019). Host plant and population source drive diversity of microbial gut communities in two polyphagous insects. Scientific Reports, 9(1), 1–11. https://doi.org/10.1038/s41598-019-39163-9Test; Kaczmarczyk, A., Kucharczyk, H., Kucharczyk, M., Kapusta, P., Sell, J., & Zielińska, S. (2018). First insight into microbiome profile of fungivorous thrips Hoplothrips carpathicus (Insecta: Thysanoptera) at different developmental stages: molecular evidence of Wolbachia endosymbiosis. Scientific Reports, 8(1), 14376. https://doi.org/10.1038/s41598-018-32747-xTest; Kadirvel, P., Srinivasan, R., Hsu, Y.-C., Su, F.-C., & De La Peña, R. (2013). Application of cytochrome oxidase I sequences for phylogenetic analysis and identification of thrips species occurring on vegetable crops. Journal of Economic Entomology, 106(1), 408–418. https://doi.org/10.1603/EC12119Test; Kaibara, F., Liyama, K., Chieda, Y., Lee, J. M., Kusakabe, T., Yasunaga-aoki, C., & Shimizu, S. (2012). Construction of serralysin-like metalloprotease-deficient mutants of Serratia liquefaciens and their virulence in the silkworm , Bombyx mori. Journal of Insect Biotechnology and Sericologynsect Biotechnology and Sericology, 81, 55–61.; Karami, M., Moosa-Kazemi, S. H., Oshaghi, M. A., Vatandoost, H., Sedaghat, M. M., Rajabnia, R., … Ferdosi-Shahandashti, E. (2016). Wolbachia endobacteria in natural populations of Culex pipiens of Iran and its phylogenetic congruence. Journal of Arthropod-Borne Diseases, 10(3), 347–363.; Kikuchi, Y., Hayatsu, M., Hosokawa, T., Nagayama, A., Tago, K., & Fukatsu, T. (2012). Symbiont-mediated insecticide resistance. Proceedings of the National Academy of Sciences, 109(22), 8618–8622. https://doi.org/10.1073/pnas.1200231109Test; Kim, B. R., Shin, J., Guevarra, R. B., Lee, J. H., Kim, D. W., Seol, K. H., … Isaacson, R. E. (2017). Deciphering diversity indices for a better understanding of microbial communities. Journal of Microbiology and Biotechnology, 27(12), 2089–2093. https://doi.org/10.4014/jmb.1709.09027Test; Kostiainen, T. S., & Hoy, M. A. (1996). The Phytoseiidae: As Biological Control Agents of Pest Mites and Insects. 10(5), 617–623.; Krishnan, M., Bharathiraja, C., Pandiarajan, J., Prasanna, V. A., Rajendhran, J., & Gunasekaran, P. (2014). Insect gut microbiome - An unexploited reserve for biotechnological application. Asian Pacific Journal of Tropical Biomedicine, 4, S16–S21. https://doi.org/10.12980/APJTB.4.2014C95Test; Kulski, J. (2015). Next-Generation Sequencing — An Overview of the History, Tools, and “Omic” Applications. In J. Kulski (Ed.), Next Generation Sequencing - Advances, Applications and Challenges. https://doi.org/DOI:10.5772/61964Test; Kumar, D., & Kim, J. (2017). Sphingomonas olei sp. nov., with the ability to degrade aliphatic hydrocarbons, isolated from oil-contaminated soil. International Journal of Systematic and Evolutionary Microbiology, 67, 2731–2738. https://doi.org/10.1099/ijsem.0.002010Test; Kumar, S., Stecher, G., Li, M., Knyaz, C., & Tamura, K. (2018). MEGA X: Molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution, 35(6), 1547–1549. https://doi.org/10.1093/molbev/msy096Test; Kumar, S., Stecher, G., & Tamura, K. (2016). MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets. Molecular Biology and Evolution, 33(7), 1870–1874. https://doi.org/10.1093/molbev/msw054Test; Kumm, S., & Moritz, G. (2008). First detection of Wolbachia in arrhenotokous populations of thrips species (Thysanoptera: Thripidae and Phlaeothripidae) and its role in reproduction. Environmental Entomology, 37(6), 1422–1428. https://doi.org/10.1603/0046-225X-37.6.1422Test; Kuriakose, J. A., Miyashiro, S., Luo, T., Zhu, B., & McBride, J. W. (2011). Ehrlichia chaffeensis transcriptome in mammalian and arthropod hosts reveals differential gene expression and post transcriptional regulation. PLoS ONE, 6(9), e24136. https://doi.org/10.1371/journal.pone.0024136Test; Kyritsis, G. A., Augustinos, A. A., Ntougias, S., Papadopoulos, N. T., Bourtzis, K., & Cáceres, C. (2019). Enterobacter sp. AA26 gut symbiont as a protein source for Mediterranean fruit fly mass-rearing and sterile insect technique applications. BMC Microbiology, 19(Suppl 1), 1–15. https://doi.org/10.1186/s12866-019-1651-zTest; Lederberg, J., & McCray, A. T. (2001). ’ Ome Sweet ’ Omics-- A Genealogical Treasury of Words. The Scientist, 15(7), 8.; Lefoulon, E., Bain, O., Makepeace, B. L., D’Haese, C., Uni, S., Martin, C., & Gavotte, L. (2016). Breakdown of coevolution between symbiotic bacteria Wolbachia and their filarial hosts. PeerJ, 2016(3), 1–30. https://doi.org/10.7717/peerj.1840Test; Lemos, L. N., Fulthorpe, R. R., Triplett, E. W., & Roesch, L. F. W. (2011). Rethinking microbial diversity analysis in the high throughput sequencing era. Journal of Microbiological Methods, 86(1), 42–51. https://doi.org/10.1016/j.mimet.2011.03.014Test; Leung, E. T., Noronha, R., Mirza, A., Shenwai, R., & Mpatziakas, A. (2018). ShinyDiversity - Understanding Alpha and Beta Diversity through Interactive Visualizations [version 1; peer review: 1 approved, 1 approved with reservations]. F1000Research, 7, 479. https://doi.org/https://doi.org/10.12688/f1000research.14217.1Test; Liberti, J., & Engel, P. (2020). The gut microbiota - brain axis of insects. Current Opinion in Insect Science, 39, 6–13. https://doi.org/10.1016/j.cois.2020.01.004Test; Librado, P., & Rozas, J. (2009). DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics, 25(11), 1451–1452. https://doi.org/10.1093/bioinformatics/btp187Test; Liu, H., Li, H., Song, F., Gu, W., Feng, J., Cai, W., & Shao, R. (2017). Novel insights into mitochondrial gene rearrangement in thrips (Insecta: Thysanoptera) from the grass thrips, Anaphothrips obscurus. Scientific Reports, 7, 4284. https://doi.org/10.1038/s41598-017-04617-5Test; Lo, N., Casiraghi, M., Salati, E., Bazzochi, C., & Bandi, C. (2002). How Many Wolbachia Supergroups Exist? Mol Biol Evo, 19(3), 341–346. https://doi.org/10.1093/oxfordjournals.molbev.a004087Test; Lopes da Silva, A., Fontoura da Silva, N., Pires, L. L., Ferreira, H., Braz, V., & Dos Santos, L. (2003). EFICIÊNCIA AGRONÔMICA DE INSETICIDAS NO CONTROLE DO Thrips tabaci LIND ., 1888 ( THYSANOPTERA , THRIPIDAE ) NA CULTURA DO ALHO 1. Pesquisa Agropecária Tropical, 33(1), 39–42.; Lozupone, C. A., Stombaugh, J. I., Gordon, J. I., Jansson, J. K., & Knight, R. (2012). Diversity, stability and resilience of the human gut microbiota. Nat Methods, 489, 220–230. https://doi.org/10.1038/nature11550Test; Maldonado Zamora, F. I., Ramírez Dávila, J. F., Rubí Arriaga, M., Antonio Némiga, X., & Lara Díaz, A. V. (2017). Distribución espacial de trips en aguacate en Coatepec Harinas, Estado de México. Revista Mexicana de Ciencias Agrícolas, 7(4), 845–856. https://doi.org/10.29312/remexca.v7i4.259Test; Marchesi, J. R., & Ravel, J. (2015). The vocabulary of microbiome research : a proposal. Microbiome, 3, 1–3. https://doi.org/10.1186/s40168-015-0094-5Test; Martin, D. P., Murrell, B., Golden, M., Khoosal, A., & Muhire, B. (2015). RDP4 : Detection and analysis of recombination patterns in virus genomes. Virus Evolution, 1(1), vev003. https://doi.org/10.1093/ve/vev003Test; Martin, J. E. (comp. . (1977). The insects and arachnids of Canada. Part 1. Collecting, preparing, and preserving insects, mites and spiders. Kromar Printing Ltd. Québec.; Marullo, R. (2009). Host-plant ranges and pest potential: habits of some thrips species in areas of southern Italy. Bulletin of Insectology, 62(2), 253–255.; Mason, K. L., Stepien, T. a, Blum, J. E., Holt, J. F., Labbe, N. H., Rush, J. S., & Raffa, K. F. (2011). From Commensal to Pathogen: Translocation of. MBio, 2(3), 1–7. https://doi.org/10.1128/mBio.00065-11.EditorTest; McMurdie, P. J., & Holmes, S. (2013). Phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data. PLoS ONE, 8(4). https://doi.org/10.1371/journal.pone.0061217Test; Meyer, C. P., & Paulay, G. (2005). DNA barcoding: Error rates based on comprehensive sampling. PLoS Biology, 3(12), e422. https://doi.org/10.1371/journal.pbio.0030422Test; Ministerio de Agricultura. (2018). Área, Producción y Rendimiento Nacional de aguacate. Retrieved February 3, 2019, from Agronet website: https://www.agronet.gov.co/Paginas/inicio2.aspxTest; Ministry, B. C. (2006). Thrips - Biology & Control.; Monje, B., Delgadillo, D., Gómez, J., & Varón, E. (2012). Manejo de Neohydatothrips signifer Priesner (Thysanoptera: Thripidae) en maracuyá (Passiflora edulis f. flavicarpa Degener) en el departamento del Huila (Colombia). Ciencia Y Tecnología Agropecuaria, 13(1), 21–30. https://doi.org/10.21930/rcta.vol13_num1_art:236Test; Moreno, C. X., Moy, F., Daniels, T. J., Godfrey, H. P., & Cabello, F. C. (2006). Molecular analysis of microbial communities identified in different developmental stages of Ixodes scapularis ticks from Westchester and Dutchess Counties, New York. Environmental Microbiology, 8(5), 761–772. https://doi.org/10.1111/j.1462-2920.2005.00955.xTest; Moritz, C., & Cicero, C. (2004). DNA barcoding: Promise and pitfalls. PLoS Biology, 2, e354. https://doi.org/10.1371/journal.pbio.0020354Test; Moritz, G., Paulsen, M., Delker, C., Picl, S., & Kumm, S. (2002). Identification of thrips using ITS-RFLP analysis. Thrips and Tospoviruses: Proceedings of the 7Th International Symposium on Thysanoptera, 365–367.; Morse, J, & Hoddle, M. (2006). Invasion Biology of Thrips. Annual Review of Entomology, 51(1), 67–89. https://doi.org/10.1146/annurev.ento.51.110104.151044Test; Morse, Joseph, & Grafton-cardwell, B. (2012). Management of citrus thrips to reduce the evolution of resistance. (April).; Mouden, S., Sarmiento, K. F., Klinkhamer, P., & Leiss, K. (2017). Integrated pest management in western flower thrips: past, present and future. Pest Management Science, 73, 813–822. https://doi.org/10.1002/ps.4531Test; Mound, L. (2005). THYSANOPTERA : Diversity and Interactions. Annual Review of Entomology, 50, 247–269. https://doi.org/10.1146/annurev.ento.49.061802.123318Test; Mound, L. A., Nielsen, M., & Hastings, A. (2017). Thysanoptera Aotearoa – Thrips of New Zealand. Retrieved March 3, 2020, from Lucidcentral.org, Identic Pty Ltd website: https://keys.lucidcentral.org/keys/v3/nz_thrips/authors.htmlTest; Mound, L., & Hoddle, M. (2016). The Scirtothrips perseae species-group (Thysanoptera), with one new species from avocado, Persea americana. Zootaxa, 4079(3), 388–392. https://doi.org/http://doi.org/10.11646/zootaxa.4079.3.7Test; Mound, L., & Teulon, D. (1995). Thysanoptera as Phytophagous Opportunist. Thrips Biology and Management, 276, 3–19. https://doi.org/10.1007/978-1-4899-1409-5Test; Mound, Laurence A., & Marullo, R. (1996). The thrips of central and south America: An introduction (Insecta: Thysanoptera). Memoirs on Entomology, International (V. Upta, Ed.). https://doi.org/10.2307/3495826Test; Mound, Laurence A. (2013). Homologies and Host-Plant Specificity : Recurrent Problems in the Study of Thrips. Florida Entomologist, 96(2), 318–322.; Muyzer, G. (1999). DGGE/TGGE a method for identifying genes from natural ecosystems. Current Opinion in Microbiology, 2(3), 317–322. https://doi.org/10.1016/S1369-5274Test(99)80055-1; Nakahara, S. (1991). Systematics of Thysanoptera, Pear thrips and other economic species. In B. Parker, M. Skinner, Lewis, & Trevor (Eds.), Towards Understanding Thysanoptera (pp. 41–59). U.S. Department of Agriculture, Forest Service, Northeastern Forest Experiment Station.; Navas-molina, J. A., Peralta-sánchez, J. M., González, A., McMurdie, P., Vasquez-Baeza, Y., Xu, Z., … Knight, R. (2013). Advancing Our Understanding of the Human Microbiome Using QIIME. Methods in Enzimology, 531, 371–444. https://doi.org/10.1016/B978-0-12-407863-5.00019-8Test; Neelakanta, G., Sultana, H., Fish, D., Anderson, J. F., & Fikrig, E. (2010). Anaplasma phagocytophilum induces Ixodes scapularis ticks to express an antifreeze glycoprotein gene that enhances their survival in the cold. Journal of Clinical Investigation, 120(9), 3179–3190. https://doi.org/10.1172/JCI42868DS1Test; Nguyen, D. T., Morrow, J. L., Spooner-Hart, R. N., & Riegler, M. (2017). Independent cytoplasmic incompatibility induced by Cardinium and Wolbachia maintains endosymbiont co-infections in haplodiploid thrips populations. Evolution, 71(4), 995–1008. https://doi.org/10.1111/evo.13197Test; Nguyen, D. T., Spooner-hart, R. N., & Riegler, M. (2015). Polyploidy versus endosymbionts in obligately thelytokous thrips. BMC Evolutionary Biology, 15(23), 1–12. https://doi.org/10.1186/s12862-015-0304-6Test; Osorio, C. R., Collins, M. D., Romalde, J. L., & Toranzo, A. E. (2005). Variation in 16S-23S rRNA Intergenic Spacer Regions in Photobacterium damselae: a Mosaic-Like Structure. Applied and Environmental Microbiology, 71(2), 636–645. https://doi.org/10.1128/AEM.71.2.636Test; Paddock, C. D., & Childs, J. E. (2003). Ehrlichia chaffeensis : a Prototypical Emerging Pathogen. Clinical Microbiology Reviews, 16(1), 37–64. https://doi.org/10.1128/CMR.16.1.37-64.2003Test; Paliy, O., & Shankar, V. (2016). Application of multivariate statistical techniques in microbial ecology. Molecular Ecology, 25(5), 1032–1057. https://doi.org/10.1111/mec.13536Test; Parada, A. E., Needham, D. M., & Fuhrman, J. A. (2016). Every base matters: Assessing small subunit rRNA primers for marine microbiomes with mock communities, time series and global field samples. Environmental Microbiology, 18(5), 1403–1414. https://doi.org/10.1111/1462-2920.13023Test; Parkinson, N., Aritua, V., Heeney, J., Cowie, C., Bew, J., & Stead, D. (2007). Phylogenetic analysis of Xanthomonas species by comparison of partial gyrase B gene sequences. International Journal of Systematic and Evolutionary Microbiology, 57(12), 2881–2887. https://doi.org/10.1099/ijs.0.65220-0Test; Parkinson, N., Cowie, C., Heeney, J., & Stead, D. (2009). Phylogenetic structure of Xanthomonas determined by comparison of gyrB sequences. International Journal of Systematic and Evolutionary Microbiology, 59(2), 264–274. https://doi.org/10.1099/ijs.0.65825-0Test; Peeters, K., & Willems, A. (2011). The gyrB gene is a useful phylogenetic marker forexploring the diversity of Flavobacterium strains isolated from terrestrial and aquatic habitats in Antarctica. FEMS Microbiology Letters, 321, 130–140. https://doi.org/10.1111/j.1574-6968.2011.02326.xTest; Pérez-Jaramillo, J. E., Carrión, V. J., Bosse, M., Ferrão, L. F. V., De Hollander, M., Garcia, A. A. F., … Raaijmakers, J. M. (2017). Linking rhizosphere microbiome composition of wild and domesticated Phaseolus vulgaris to genotypic and root phenotypic traits. ISME Journal, 11(10), 2244–2257. https://doi.org/10.1038/ismej.2017.85Test; Pham, V. H. T., & Kim, J. (2016). Improvement for Isolation of Soil Bacteria by Using Common Culture Media. Journal of Pure and Applied Microbiology, 10(1), 1–11.; Pileggi, M., Alvim, S., Pileggi, V., Olchanheski, R., Garbugio, P., Munoz, A. M., … Sadowsky, M. (2012). Isolation of mesotrione - degrading bacteria from aquatic environments in Brazil. Chemosphere, 86(11), 1127–1132. https://doi.org/10.1016/j.chemosphere.2011.12.041Test; Powell, C. M., Lopez Montiel, A., Beddingfield, B., Hanson, J. D., & Bextine, B. R. (2015). Comparison of bacterial communities of flower thrips (Frankliniella tritici) and potato psyllid (Bactericera cockerelli). Southwestern Entomologist, 40(4), 765–773. https://doi.org/10.3958/059.040.0404Test; Puillandre, N., Lambert, A., Brouillet, S., & Achaz, G. (2012). ABGD, Automatic Barcode Gap Discovery for primary species delimitation. Molecular Ecology, 21(8), 1864–1877. https://doi.org/10.1111/j.1365-294X.2011.05239.xTest; Ramirez-Ahuja, M. de L., Gómez-Govea, M. A., Lugo-Trampe, A., Borrego-Soto, G., Delgado-Enciso, I., Ponce-Garcia, G., … Rodriguez-Sanchez, I. R. (2019). Microbiota of Telenomus tridentatus ( Platygastroidea : Scelionidae ): An unwanted parasitoid. Applied Entomology, (May), 1–8. https://doi.org/10.1111/jen.12656Test; Rebijith, K. B., Asokan, R., Krishna, V., Ranjitha, H. H., Krishna Kumar, N. K., & Ramamurthy, V. V. (2014). DNA Barcoding and Elucidation of Cryptic Diversity in Thrips (Thysanoptera). Florida Entomologist, 97(4), 1328–1347. https://doi.org/10.1653/024.097.0407Test; Reece, R. J., & Maxwell, A. (1991). DNA Gyrase: Structure and Function. Critical Reviews in Biochemistry and Molecular Biology, 26(3–4), 335–375. https://doi.org/10.3109/10409239109114072Test; Reitz, S. R. (2009). Biology and Ecology of the Western Flower Thrips (Thysanoptera: Thripidae): The Making of a Pest. Florida Entomologist, 92(1), 7–13. https://doi.org/10.1653/024.092.0102Test; Rendón-Anaya, M., Ibarra-Laclette, E., Méndez-Bravo, A., Lan, T., Zheng, C., Carretero-Paulet, L., … Herrera-Estrella, L. (2019). The avocado genome informs deep angiosperm phylogeny, highlights introgressive hybridization, and reveals pathogen-influenced gene space adaptation. Proceedings of the National Academy of Sciences of the United States of America, 116(34), 17081–17089. https://doi.org/10.1073/pnas.1822129116Test; Restrepo-Quiroz, T., & Arango-Isaza, R. (2014). Aislamiento, identificación y evaluación de hongos entomopatógenos como posibles agentes de control de trips (Thysanoptera: Thripidae ) asociados a cultivos de aguacate (Persea americana Miller) (Universidad Nacional de Colombia). Retrieved from http://bdigital.unal.edu.co/49548/1/1037590998.2015.pdfTest; Reynaud, P. (2010). Thrips ( Thysanoptera ). Chapter 13.1. Biodiversity and Ecosystem Risk Assessment, 4(2), 767–791. https://doi.org/10.3897/biorisk.4.59Test; Rikihisa, Y. (2006). Ehrlichia subversion of host innate responses. Current Opinion in Microbiology, 9(1), 95–101. https://doi.org/10.1016/j.mib.2005.12.003Test; Rios-Castaño, D. (2003). Variedades De Aguacate Para El Trópico : Actas V Congreso Mundial Del Aguacate, 143–147.; Rodicio, M. D. R., & Mendoza, M. D. C. (2004). Identificación bacteriana mediante secuenciación del ARNr 16S: fundamento, metodología y aplicaciones en microbiología clínica. Enfermedades Infecciosas y Microbiología Clínica, 22(4), 238–245. https://doi.org/10.1157/13059055Test; Ronquist, F., Teslenko, M., Van Der Mark, P., Ayres, D. L., Darling, A., Höhna, S., … Huelsenbeck, J. P. (2012). Mrbayes 3.2: Efficient bayesian phylogenetic inference and model choice across a large model space. Systematic Biology, 61(3), 539–542. https://doi.org/10.1093/sysbio/sys029Test; Ros, V. I. D., Fleming, V. M., Feil, E. J., & Breeuwer, J. A. J. (2009). How diverse is the genus Wolbachia? Multiple-gene sequencing reveals a putatively new Wolbachia supergroup recovered from spider mites (Acari: Tetranychidae). Applied and Environmental Microbiology, 75(4), 1036–1043. https://doi.org/10.1128/AEM.01109-08Test; Rosenberg, E. (2017). Evolution: From Darwin to the Hologenome Concept. In It’s in Your DNA (pp. 139–153). https://doi.org/10.1016/B978-0-12-812502-1/00015-9Test; Rozas, J., Ferrer-Mata, A., Sánchez-DelBarrio, J. C., Guirao-Rico, S., Librado, P., Ramos-Onsins, S. E., & Sánchez-Gracia, A. (2017). DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets. Molecular Biology and Evolution, 34(12), 3299–3302. Retrieved from http://dx.doi.org/10.1093/molbev/msx248Test; Rugman-Jones, P., Hoddle, M., Mound, L., & Stouthamer, R. (2006). Molecular Identification Key for Pest Species of Scirtothrips (Thysanoptera: Thripidae). Journal Economic Entomology, 99(5), 1813–1819. https://doi.org/10.1603/0022-0493-99.5.1813Test; Sanders, E. R., & Miller, J. H. (2010). I, microbiologist: a discovery-based course in microbial ecology and molecular evolution. https://doi.org/10.1080/00219266.2011.645852Test; Saurav, G., Daimei, G., Singh, V. R., Popli, S., & Rajagopal, R. (2016). Detection and Localization of Wolbachia in Thrips palmi Karny (Thysanoptera: Thripidae). Indian Journal of Microbiology, 1–5. https://doi.org/10.1007/s12088-016-0567-7Test; Scholz, M. B., Lo, C., & Chain, P. S. G. (2012). Next generation sequencing and bioinformatic bottlenecks: the current state of metagenomic data analysis. Current Opinion in Biotechnology, 23, 9–15. https://doi.org/10.1016/j.copbio.2011.11.013Test; Schulenburg, J. H. G. v. d., Hurst, G. D. D., Huigens, T. M. E., Van Meer, M. M. M., Jiggins, F. M., & Majerus, M. E. N. (2000). Molecular evolution and phylogenetic utility of Wolbachia ftsZ and wsp gene sequences with special reference to the origin of male-killing. Molecular Biology and Evolution, 17(4), 584–600. https://doi.org/10.1093/oxfordjournals.molbev.a026338Test; Seepiban, C., Charoenvilaisiri, S., Kumpoosiri, M., Bhunchoth, A., Chatchawankanphanich, O., & Gajanandana, O. (2015). Development of a protocol for the identification of tospoviruses and thrips species in individual thrips. Journal of Virological Methods, 222, 206–213. https://doi.org/http://dx.doi.org/10.1016/j.jviromet.2015.06.017Test; Shafi, J., Tian, H., & Ji, M. (2017). Bacillus species as versatile weapons for plant pathogens: a review. Biotechnology and Biotechnological Equipment, 31(3), 446–459. https://doi.org/10.1080/13102818.2017.1286950Test; Shao, R., & Barker, S. C. (2003). The highly rearranged mitochondrial genome of the plague thrips, Thrips imaginis (insecta: Thysanoptera): Convergence of two novel gene boundaries and an extraordinary arrangement of rRNA genes. Molecular Biology and Evolution, 20(3), 362–370. https://doi.org/10.1093/molbev/msg045Test; Sheik, C. S., Beasley, W. H., Elshahed, M. S., Zhou, X., Luo, Y., & Krumholz, L. R. (2011). Effect of warming and drought on grassland microbial communities. The ISME Journal, 5, 1692–1700. https://doi.org/10.1038/ismej.2011.32Test; Shelomi, M. (2019). Journal of Asia-Paci fi c Entomology Bacterial and eukaryote microbiomes of mosquito habitats in dengue- endemic southern Taiwan. Journal of Asia-Pacific Entomology, 22(2), 471–480. https://doi.org/10.1016/j.aspen.2019.02.011Test; Silva-Bedoya, L. M., Sánchez-Pinzón, M. S., Cadavid-Restrepo, G. E., & Moreno-Herrera, C. X. (2016). Bacterial community analysis of an industrial wastewater treatment plant in Colombia with screening for lipid-degrading microorganisms. Microbiological Research, 192, 313–325. https://doi.org/10.1016/j.micres.2016.08.006Test; Sivakumar, G., Rangeshwaran, R., Yandigeri, M., Mohan, M., Venkatesan, T., Ballal, C., … Verghese, A. (2017). Characterization and role of gut bacterium Bacillus pumilus on nutrition and defense of leafhopper ( Amrasca biguttula) of cotton. Indian Journal of Agricultural Sciences, 87(4), 534–539.; Sommer, F., & Bäckhed, F. (2013). The gut microbiota-masters of host development and physiology. Nature Reviews Microbiology, 11(4), 227–238. https://doi.org/10.1038/nrmicro2974Test; Souza, H. V., Marchesin, S. R. C., & Itoyama, M. M. (2016). Analysis of the mitochondrial COI gene and its informative potential for evolutionary inferences in the families Coreidae and Pentatomidae (Heteroptera). Genetics and Molecular Research, 15(1), 1–14. https://doi.org/10.4238/gmr.15017428Test; Srivastava, N., Gupta, B., Gupta, S., Danquah, M. K., & Sarethy, I. P. (2019). Analyzing Functional Microbial Diversity : An Overview of Techniques. In Microbial Diversity in the Genomic Era. https://doi.org/10.1016/B978-0-12-814849-5.00006-XTest; Stirling, G., & Wilsey, B. (2013). Empirical Relationships between Species Richness, Evenness, and Proportional Diversity. The American Naturalist, 158(3), 286–299. https://doi.org/10.1086/321317Test .; Stracy, M., Wollman, A., Kaja, E., Gapinski, J., Lee, J., Leek, V. A., … Zawadzki, P. (2019). Single-molecule imaging of DNA gyrase activity in living Escherichia coli. Nucleic Acids Research, 47(1), 210–220. https://doi.org/10.1093/nar/gky1143Test; Suen, G., Scott, J. J., Aylward, F. O., Adams, S. M., Tringe, S. G., Pinto-Tomás, A. A., … Currie, C. R. (2010). An insect herbivore microbiome with high plant Biomass-degrading capacity. PLoS Genetics, 6(9), 1–14.; Suen, G., Scott, J. J., Aylward, F. O., Adams, S. M., Tringe, S. G., Pinto-Tomás, A. A., … Currie, C. R. (2010). An insect herbivore microbiome with high plant Biomass-degrading capacity. PLoS Genetics, 6(9), 1–14. https://doi.org/10.1371/journal.pgen.1001129Test; Teng, F., Sankar, S., Zhu, P., Li, S., Huang, S., Li, X., … Yang, F. (2018). Impact of DNA extraction method and targeted 16S-rRNA hypervariable region on oral microbiota profiling. Scientific Reports, 8, 16321. https://doi.org/10.1038/s41598-018-34294-xTest; ThripsWiki. (2019). ThripsWiki - providing information on the World’s thrips. Retrieved February 1, 2019, from http://thrips.info/wiki/Main_PageTest; Turcios-Palomo, C. L. A. (2013). Identificación y Fluctuación Poblacional de Trips (Insecta: Thysanoptera) Asociados con Hortalizas de la Región Central de México. 67.; Tyagi, K., Kumar, V., & Mound, L. A. (2008). Sexual dimorphism among Thysanoptera Terebrantia, with a new species from Malaysia and remarkable species from India in Aeolothripidae and Thripidae. Insect Systematics & Evolution, 39, 155–170. https://doi.org/doi.org/10.1163/187631208788784093Test; Tyagi, K., Kumar, V., Singha, D., Chandra, K., Laskar, B. A., Kundu, S., … Chatterjee, S. (2017). DNA Barcoding studies on Thrips in India: Cryptic species and Species complexes. Scientific Reportys, 7, 4898. https://doi.org/10.1038/s41598-017-05112-7Test; Tzec-Interián, J. A., Desgarennes, D., Carrión, G., Monribot-Villanueva, J. L., Guerrero-Analco, J. A., Ferrera-Rodríguez, O., … Ortiz-Castro, R. (2020). Characterization of plant growth-promoting bacteria associated with avocado trees (Persea americana Miller) and their potential use in the biocontrol of Scirtothrips perseae (avocado thrips). PLoS ONE, 15(4), e0231215. https://doi.org/10.1371/journal.pone.0231215Test; Ursell, L. K., Metcalf, J. L., Parfrey, L. W., & Knight, R. (2012). Definig the Human Microbiome. NIH Manuscripts, 70(Suppl 1), 1–12. https://doi.org/10.1111/j.1753-4887.2012.00493.x.DefiningTest; Van der Kooi, C. J., & Schwander, T. (2014). Evolution of asexuality via different mechanisms in grass thrips (Thysanoptera: Aptinothrips). Evolution, 68(7), 1883–1893. https://doi.org/10.1111/evo.12402Test; Varon Devia, E. H. (2014). Trips, Bichos Candela. In Actualización tecnológica y buenas prácticas agrícolas (BPA) en el cultivo de aguacate. Manual Técnico CORPOICA, Centro de Investigación la Selva (pp. 257–265). Retrieved from http://hdl.handle.net/20.500.12324/12616Test; Vavre, F., Dedeine, F., Quillon, M., Fouillet, P., Fleury, F., & Boulétreau, M. (2001). Within-species diversity of Wolbachia-induced cytoplasmic incompatibility in haplodiploid insects. Evolution, 55(8), 1710–1714. https://doi.org/http://dx.doi.org/10.1554/0014-3820Test(2001)055[1710:WSDOWI]2.0.CO;2; Vavre, F., Fouillet, P., & Fleury, F. (2003). Between- and Within-Host Species Selection on Cytoplasmic Incompatibility–Inducing Wolbachia in Haplodiploids. Evolution, 57(2), 421–427. https://doi.org/10.1111/j.0014-3820.2003.tb00275.xTest; Villareal H., M., Álvarez, S. Córdoa, F., Escobar, G., Fagua, F. Gast, H., Mendoza, M., & Umaña. M. (2004). Métodos para el análisis de datos: una aplicación para resultados provenientes de caracterizaciones de biodiversidad. Manual de Métodos Para El Desarrollo de Inventarios de Biodiversidad. Instituto de Investigación de Recursos Biológicos Alexander Von Humbolt, 188–225. https://doi.org/10.1017/CBO9781107415324.004Test; Vivero, R. J., Cadavid-Restrepo, G., Moreno Herrera, C. X., & Uribe Soto, S. I. (2017). Molecular detection and identification of Wolbachia in three species of the genus Lutzomyia on the Colombian Caribbean coast. Parasites & Vectors, 10(1), 110. https://doi.org/10.1186/s13071-017-2031-xTest; Vivero, R. J., Gil Jaramillo, N., Cadavid-Restrepo, G., Uribe Soto, S., & Moreno Herrera, C. X. (2016). Structural differences in gut bacteria communities in developmental stages of natural populations of Lutzomyia evansi from Colombia’s Caribbean coast. Parasites & Vectors, 9, 496. https://doi.org/10.1186/s13071-016-1766-0Test; Wagner, B. D., Grunwald, G. K., Zerbe, G. O., Mikulich-gilbertson, S. K., Robertson, C. E., Zemanick, E. T., & Harris, J. K. (2018). On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities. Frontiers in Microbiology, 9, 1037. https://doi.org/10.3389/fmicb.2018.01037Test; Walker, T., Johnson, P. H., Moreira, L. A., Iturbe-Ormaetxe, I., Frentiu, F. D., McMeniman, C. J., … Hoffmann, A. A. (2011). The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations. Nature, 476(7361), 450–455. https://doi.org/10.1038/nature10355Test; Walterson, A. M., Smith, D. D. N., & Stavrinides, J. (2014). Identification of a Pantoea Biosynthetic Cluster That Directs the Synthesis of an Antimicrobial Natural Product. PLoS ONE, 9(5), 1–12. https://doi.org/10.1371/journal.pone.0096208Test; Walterson, A. M., & Stavrinides, J. (2015). Pantoea: Insights into a highly versatile and diverse genus within the Enterobacteriaceae. FEMS Microbiology Reviews, 39(6), 968–984. https://doi.org/10.1093/femsre/fuv027Test; Wang, G. H., Jia, L. Y., Xiao, J. H., & Huang, D. W. (2016). Discovery of a new Wolbachia supergroup in cave spider species and the lateral transfer of phage WO among distant hosts. Infection, Genetics and Evolution, 41, 1–7. https://doi.org/10.1016/j.meegid.2016.03.015Test; Wang, L., Lee, F., Tai, C., & Kasai, H. (2007). Comparison of gyrB gene sequences, 16S rRNA gene sequences and DNA–DNA hybridization in the Bacillus subtilis group. International Journal of Systematic and Evolutionary Microbiology, 57, 1846–1850. https://doi.org/10.1099/ijs.0.64685-0Test; Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007). Naïve Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy. Applied and Environmental Microbiology, 73(16), 5261–5267. https://doi.org/10.1128/AEM.00062-07Test; Wartell, R. M., Hosseini, S. H., & Moran, C. P. (1990). Detecting base pair substitutions in DNA fragments by temperature-gradient gel electrophoresis. Nucleic Acids Research, 18(9), 2699–2705. Retrieved from http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=330754&tool=pmcentrez&rendertype=abstractTest; Werren, J. H., Hurst, G. D. D., Zhang, W., Breeuwer, J. A. J., Stouthamer, R., & Majerus, M. E. N. (1994). Rickettsial relative associated with male killing in the ladybird beetle (Adalia bipunctata). Journal of Bacteriology, 176(2), 388–394. https://doi.org/10.1128/jb.176.2.388-394.1994Test; Werren, J. H., Zhang, W., & Guo, L. (1995). Evolution and phylogeny of Wolbachia: Reproductive parasites of arthropods. Proceedings of the Royal Society B: Biological Sciences, 261(1360), 55–71. https://doi.org/10.1098/rspb.1995.0117Test; Werren, John H., & O’Neill, S. L. (1997). The evolution of heritable symbionts. Influential Passengers: Inherited Microorganisms and Arthropod Reproduction, 3–41.; Werren, John H, Baldo, L., & Clark, M. E. (2008). Wolbachia: master manipulators of invertebrate biology. Nature Reviews Microbiology, 6, 741–751. https://doi.org/10.1038/nrmicro1969Test; Westmore, G., Poke, F., Allen, G., & Wilson, C. (2013). Genetic and host-associated differentiation within Thrips tabaci Lindeman (Thysanoptera: Thripidae) and its links to Tomato spotted wilt virus-vector competence. Heredity, 111, 210–215. https://doi.org/10.1038/hdy.2013.39Test; Woese, C. R. (1987). Bacterial Evolution. Microbiology, 51(2), 221–271. https://doi.org/10.1139/m88-093Test; Yamamoto, S., & Harayama, S. (1995). PCR Amplification and Direct Sequencing of gyrB Genes with Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas putida Strains. Applied and Environmental Microbiology, 61(3), 1104–1109.; Yan, D., Tang, Y., Xue, X., Wang, M., Liu, F., & Fan, J. (2012). The complete mitochondrial genome sequence of the western flower thrips Frankliniella occidentalis (Thysanoptera: Thripidae) contains triplicate putative control regions. Gene, 506(1), 117–124. https://doi.org/10.1016/j.gene.2012.06.022Test; Yang, B., Wang, Y., & Qian, P. (2016). Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis. BMC Bioinformatics, 17, 135. https://doi.org/10.1186/s12859-016-0992-yTest; Yang, X. H., Zhu, D. H., Liu, Z., Zhao, L., & Su, C. Y. (2013). High levels of multiple infections, recombination and horizontal transmission of Wolbachia in the Andricus mukaigawae (Hymenoptera; Cynipidae) communities. PLoS ONE, 8(11), e78970. https://doi.org/10.1371/journal.pone.0078970Test; Yim, O., & Ramdeen, K. (2015). Hierarchical Cluster Analysis : Comparison of Three Linkage Measures and Application to Psychological Data. The Quantitative Methods for Psychology, 11(1), 8–21. https://doi.org/10.20982/tqmp.11.1.p008Test; Yin, H., Cao, L., Qiu, G., Wang, D., Kellogg, L., Zhou, J., … Liu, X. (2008). Molecular diversity of 16S rRNA and gyrB genes in copper mines. Archives of Microbiology, 189(2), 101–110. https://doi.org/10.1007/s00203-007-0298-6Test; Yoshino, K., Nishigaki, K., & Husimi, Y. (1991). Temperature sweep gel electrophoresis: a simple method to detect point mutations. Nucleic Acids Research, 19(11), 3153.; Yun, J., Roh, W., Whon, W., Jung, M., Kim, M., Park, D., … Bae, J.-W. (2014). Insect Gut Bacterial Diversity Determined by Environmental Habitat , Diet , Developmental Stage , and Phylogeny of Host. Applied and Environmental Microbiology, 80(17), 5254–5264. https://doi.org/10.1128/AEM.01226-14Test; Zabal-Aguirre, M., Arroyo, F., García-Hurtado, J., De la Torre, J., Hewitt, G. M., & Bella, J. L. (2014). Wolbachia effects in natural populations of Chorthippus parallelus from the Pyrenean hybrid zone. Journal of Evolutionary Biology, 27(6), 1136–1148. https://doi.org/10.1111/jeb.12389Test; Zapata, J. C., & Leal, J. M. (2018). Manejo integrado de la pudrición de raíces del aguacate (Persea americana Miller), causada por Phytophthora cinnamomi Rands. Temas Agrarios, 23(2), 131–143. https://doi.org/https://doi.org/10.21897/rta.v23i2.1297Test; Zeh, D. W., Zeh, J. A., & Bonilla, M. M. (2005). Wolbachia, sex ratio bias and apparent male killing in the harlequin beetle riding pseudoscorpion. Heredity, 95(1), 41–49. https://doi.org/10.1038/sj.hdy.6800666Test; Zhang, X. C., & Zhang, F. (2018). The Potential Control Strategies Based on the Interaction Between Indoor Cockroaches and Their Symbionts in China. In Advances in Insect Physiology (1st ed., Vol. 55). https://doi.org/10.1016/bs.aiip.2018.07.001Test; Zhou, W., Rousset, F., & O’Neill, S. (1998). Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences. Proceedings of the Royal Society Biological Sciences, 265(1395), 509–515. https://doi.org/10.1098/rspb.1998.0324Test; Zouache, K., Voronin, D., Tran-Van, V., Mousson, L., Failloux, A., & Mavingui, P. (2009). Persistent Wolbachia and Cultivable Bacteria Infection in the Reproductive and Somatic Tissues of the Mosquito Vector Aedes albopictus. PLoS ONE, 4(7), e6388. https://doi.org/10.1371/journal.pone.0006388Test; Zug, R., & Hammerstein, P. (2012). Still a Host of Hosts for Wolbachia : Analysis of Recent Data Suggests That 40 % of Terrestrial Arthropod Species Are Infected. PLoS ONE, 7(6), e38544. https://doi.org/10.1371/journal.pone.0038544Test; https://repositorio.unal.edu.co/handle/unal/78594Test

الإتاحة: https://doi.org/10.1128/AEM.00731-06Test
https://doi.org/10.1111/1462-2920.12362Test
https://doi.org/10.1146/annurev-ento-011613-162007Test
https://doi.org/10.1038/nmeth.f.303Test
https://doi.org/10.1099/mic.0.28313-0Test
https://doi.org/10.1016/j.ijpara.2003.10.004Test
https://doi.org/10.1146/annurev.biochem.70.1.369Test
https://doi.org/10.1016/j.ijfoodmicro.2017.11.008Test
https://doi.org/10.1093/nar/gkn879Test
https://doi.org/10.1056/NEJMoa0900863Test

المؤلفون: Razakatiana, Adamson Tsoushima Ernest, Becquer, Thierry, Randriambanona, Herizo, Baohanta, Rondro Harinisainana, Andrianandrasana, Martial Doret, Le Roux, Christine, Duponnois, Robin, Ramanankierana, Heriniaina

المصدر: Scientific Papers. Series A. Agronomy

مصطلحات موضوعية: F08 - Systèmes et modes de culture, P34 - Biologie du sol, P35 - Fertilité du sol, Oryza sativa, Phaseolus vulgaris, Biologie du sol, Culture intercalaire, Symbiote, Relation plante sol, Activité biologique dans le sol, Interactions biologiques, Écologie microbienne, Azote, Phosphore, http://aims.fao.org/aos/agrovoc/c_5438Test, http://aims.fao.org/aos/agrovoc/c_5767Test, http://aims.fao.org/aos/agrovoc/c_7160Test, http://aims.fao.org/aos/agrovoc/c_3910Test, http://aims.fao.org/aos/agrovoc/c_7562Test, http://aims.fao.org/aos/agrovoc/c_16146Test, http://aims.fao.org/aos/agrovoc/c_9264Test, http://aims.fao.org/aos/agrovoc/c_49896Test, http://aims.fao.org/aos/agrovoc/c_24111Test, http://aims.fao.org/aos/agrovoc/c_5192Test, http://aims.fao.org/aos/agrovoc/c_5804Test

وصف الملف: text

العلاقة: http://agritrop.cirad.fr/597096Test/; Microbial symbionts and nutrient (N and P) sharing: Effect on soil microbial activity in the upland rice (Oriza sativa) and bean (Phaseolus vulgaris) intercropping. Razakatiana Adamson Tsoushima Ernest, Becquer Thierry, Randriambanona Herizo, Baohanta Rondro Harinisainana, Andrianandrasana Martial Doret, Le Roux Christine, Duponnois Robin, Ramanankierana Heriniaina. 2020. Scientific Papers. Series A. Agronomy, 63 (1) : 490-499.http://agronomyjournal.usamv.ro/index.php/18-articles/articles-2019-issue-1/1105-microbial-symbionts-and-nutrients-n-and-p-sharing-effect-on-soil-microbial-activity-in-the-upland-rice-oriza-sativa-and-bean-phaseolus-vulgaris-intercroppingTest; http://agritrop.cirad.fr/597096/1/Razakatiana%202020%20MICROBIAL%20SYMBIONTS%20rice%20and%20bean%20.pdfTest

الإتاحة: http://agritrop.cirad.fr/597096Test/
http://agritrop.cirad.fr/597096/1/Razakatiana%202020%20MICROBIAL%20SYMBIONTS%20rice%20and%20bean%20.pdfTest
http://agronomyjournal.usamv.ro/index.php/18-articles/articles-2019-issue-1/1105-microbial-symbionts-and-nutrients-n-and-p-sharing-effect-on-soil-microbial-activity-in-the-upland-rice-oriza-sativa-and-bean-phaseolus-vulgaris-intercroppingTest

المؤلفون: Noda, Hiroaki, Miyoshi, Takeharu

المصدر: In Vitro Cellular & Developmental Biology. Animal, 2002 Jul 01. 38(7), 423-427.

الوصول الحر: https://www.jstor.org/stable/4295378Test

المؤلفون: Frago, Enric, Zytynska, Sharon E.

المصدر: Current Opinion in Insect Science

مصطلحات موضوعية: L72 - Organismes nuisibles des animaux, parasitoïde, hôte, ponte, agent de lutte biologique, symbiote, http://aims.fao.org/aos/agrovoc/c_34070Test, http://aims.fao.org/aos/agrovoc/c_3673Test, http://aims.fao.org/aos/agrovoc/c_5462Test, http://aims.fao.org/aos/agrovoc/c_920Test, http://aims.fao.org/aos/agrovoc/c_7562Test

وصف الملف: text

العلاقة: http://agritrop.cirad.fr/608538Test/; Impact of herbivore symbionts on parasitoid foraging behaviour. Frago Enric, Zytynska Sharon E. 2023. Current Opinion in Insect Science, 57:101027, 7 p.https://doi.org/10.1016/j.cois.2023.101027Test; http://agritrop.cirad.fr/608538/1/ID608538.pdfTest

الإتاحة: https://doi.org/10.1016/j.cois.2023.101027Test
http://agritrop.cirad.fr/608538Test/
http://agritrop.cirad.fr/608538/1/ID608538.pdfTest

المؤلفون: Hafsi, Abir, Delatte, Hélène

المصدر: Biological Invasions

مصطلحات موضوعية: H10 - Ravageurs des plantes, C30 - Documentation et information, Enterobacteriaceae, Symbiote, Espèce envahissante, Facilitation des échanges, Dynamique des populations, Tephritidae, Infestation, http://aims.fao.org/aos/agrovoc/c_2580Test, http://aims.fao.org/aos/agrovoc/c_7562Test, http://aims.fao.org/aos/agrovoc/c_49865Test, http://aims.fao.org/aos/agrovoc/c_ef43b6efTest, http://aims.fao.org/aos/agrovoc/c_6111Test, http://aims.fao.org/aos/agrovoc/c_3122Test, http://aims.fao.org/aos/agrovoc/c_3855Test

وصف الملف: text

العلاقة: http://agritrop.cirad.fr/603049Test/; Enterobactereaceae symbiont as facilitators of biological invasion: Review on Tephritidae fruit flies. Hafsi Abir, Delatte Hélène. 2023. Biological Invasions, 25 : 991-1006.https://doi.org/10.1007/s10530-022-02960-xTest; http://agritrop.cirad.fr/603049/7/603049ed.pdfTest

الإتاحة: https://doi.org/10.1007/s10530-022-02960-xTest
http://agritrop.cirad.fr/603049Test/
http://agritrop.cirad.fr/603049/7/603049ed.pdfTest

المؤلفون: Lorenzo Imbesi

المساهمون: Imbesi, Lorenzo

مصطلحات موضوعية: autopoiesi, cyborg, homo technologicu, technological framework, scot, symbiote, tecnoscience

العلاقة: info:eu-repo/semantics/altIdentifier/isbn/9788832080193; volume:67/19; firstpage:34; lastpage:41; numberofpages:8; journal:DIID. DISEGNO INDUSTRIALE INDUSTRIAL DESIGN; http://hdl.handle.net/11573/1515455Test

الإتاحة: http://hdl.handle.net/11573/1515455Test