Molecular mechanisms of ceftazidime resistance in Pseudomonas aeruginosa isolates from canine and human infections

التفاصيل البيبلوغرافية
العنوان: Molecular mechanisms of ceftazidime resistance in Pseudomonas aeruginosa isolates from canine and human infections
المؤلفون: Hen-Wei Wei, S. J. Du, H. C. Kuo, Shao-Kuang Chang, Andrew Chang-Young Fei, Chiung-Hsiang Cheng
المصدر: Veterinární medicína. 55:172-182
بيانات النشر: Czech Academy of Agricultural Sciences, 2010.
سنة النشر: 2010
مصطلحات موضوعية: 0301 basic medicine, General Veterinary, medicine.drug_class, Pseudomonas aeruginosa, medicine.medical_treatment, 030106 microbiology, Antibiotics, Cephalosporin, Ceftazidime, Drug resistance, biochemical phenomena, metabolism, and nutrition, Biology, bacterial infections and mycoses, medicine.disease_cause, Microbiology, Multiple drug resistance, 03 medical and health sciences, medicine, Beta-lactamase, Efflux, medicine.drug
الوصف: Sixty-six clinical P. aeruginosa isolates, 17 obtained from canine otitis specimens and 49 received from human patients with bloodstream infections, were collected between February 2007 and January 2008. The minimal inhibitory concentrations (MICs) of the antimicrobial agents of these isolates were determined. Multidrug resistance was common, with 23 (34.8%) isolates found to be ceftazidime resistant. To explore the mechanisms of ceftazidime resistance, PCR analyses were performed to detect drug-resistance genes. The prevalence rate of Ambler class A, B, and D β-lactamase genes were obtained, with bla TEM-1 100%, bla PSE-1 100%, bla OXA-2 96.2%, bla SHV-18 91.3%, bla OXA-17 78.3%, bla VIM-3 26.1%, bla OXA-10 21.7% and bla SHV-1 8.7%. An efflux inhibition assay with the PAβN compound was conducted. The ceftazidime resistance isolates were also tested by RT-qPCR to deter- mine the mRNA expression levels of the oprM and ampC genes. Five (21.7%) of the ceftazidime resistance iso- lates appeared to overactivate the OprM efflux system. The ampD, ampE, and ampR genes and the ampC-ampR intergenic region were subsequently amplified and sequenced. Five (21.7%) of the ceftazidime resistance isolates from humans and canines had a point mutation in AmpR (Asp135-Asn, n = 3; Als194-Ser, n = 2), which induces AmpC overproduction from 10- to 80-fold. T his study first reported ceftazidime resistance in P. aeruginosa from canine otitis specimens, which are closely related to ESBLs (50%), including the overproduction of AmpC (25%) and the OprM efflux system (25%). The ESBLs (100%) played an important role in all ceftazidime resistance iso- lates from humans, and either AmpC (21.1%) or OprM (21.1%) might be overexpressed within the same isolate. A human patient isolate (H307B) showed simultaneous expression of ESBLs, the OprM efflux system, and AmpC overproduction.
تدمد: 1805-9392
0375-8427
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::06e1c0b8a93f109b91718768fa48eb3fTest
https://doi.org/10.17221/64/2010-vetmedTest
حقوق: OPEN
رقم الانضمام: edsair.doi...........06e1c0b8a93f109b91718768fa48eb3f
قاعدة البيانات: OpenAIRE