دورية أكاديمية

Role of inducers in detection of blaPDC-mediated oxyimino-cephalosporin resistance in Pseudomonas aeruginosa

التفاصيل البيبلوغرافية
العنوان: Role of inducers in detection of blaPDC-mediated oxyimino-cephalosporin resistance in Pseudomonas aeruginosa
المؤلفون: Birson Ingti, Deepika B Krishnatreya, Anand Prakash Maurya, Debadatta Dhar (Chanda), Atanu Chakravarty, Amitabha Bhattacharjee
المصدر: Indian Journal of Medical Research, Vol 145, Iss 5, Pp 659-664 (2017)
بيانات النشر: Wolters Kluwer Medknow Publications
سنة النشر: 2017
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: AmpC β-lactamase - blaPDC- Pseudomonas aeruginosa, Medicine
الوصف: Background & objectives: Pseudomonas aeruginosa possessing chromosomally inducible blaPDCalong with other intrinsic mechanism causes infection with high mortality rate. It is difficult to detect inducible AmpC enzymes in this organism and is usually overlooked by routine testing that may lead to therapeutic failure. Therefore, three different inducers were evaluated in the present study to assess their ability of induction of blaPDCin P. aeruginosa. Methods: A total of 189 consecutive Pseudomonas isolates recovered from different clinical specimens (November 2011-April 2013) were selected for the study. Isolates were screened with cefoxitin for AmpC β-lactamases and confirmed by modified three-dimensional extract test (M3DET). Inductions were checked using three inducers, namely, clavulanic acid, cefoxitin and imipenem along with ceftazidime. Molecular screening of AmpC β-lactamase genes was performed by PCR assay. Antimicrobial susceptibility and minimum inhibitory concentrations (MICs) were determined, and repetitive extragenic palindromic-PCR of all blaPDCharbouring isolates was performed. Results: Inducible phenotype was observed in 42 (24.3%) of 97 (56%) isolates confirmed by M3DET. Among these, 22 isolates harboured chromosomal blaPDCgene, and cocarriage of both chromosomal and plasmid-mediated blaAmpC genes was observed in seven isolates. Cefoxitin-ceftazidime-based test gave good sensitivity and specificity for detecting inducible AmpC enzymes. Isolates harbouring blaPDCshowed high MIC against all tested cephalosporins and monobactam. DNA fingerprinting of these isolates showed 22 different clones of P. aeruginosa. Interpretation & conclusions: P. aeruginosa harbouring inducible (chromosomal) and plasmid-mediated AmpC β-lactamase is a matter of concern as it may limit therapeutic option. Using cefoxitin-ceftazidime-based test is simple and may be used for detecting inducible AmpC β-lactamase amongst P. aeruginosa.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0971-5916
العلاقة: http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2017;volume=145;issue=5;spage=659;epage=664;aulast=IngtiTest; https://doaj.org/toc/0971-5916Test; https://doaj.org/article/00e3770e49ec46788a3e77922cd608b1Test
DOI: 10.4103/ijmr.IJMR_628_15
الإتاحة: https://doi.org/10.4103/ijmr.IJMR_628_15Test
https://doaj.org/article/00e3770e49ec46788a3e77922cd608b1Test
رقم الانضمام: edsbas.9DE495E1
قاعدة البيانات: BASE
الوصف
تدمد:09715916
DOI:10.4103/ijmr.IJMR_628_15