首页> 美国卫生研究院文献>Frontiers in Veterinary Science >Prevalence of Beta-Lactam and Quinolone/Fluoroquinolone Resistance in Enterobacteriaceae From Dogs in France and Spain—Characterization of ESBL/pAmpC Isolates Genes and Conjugative Plasmids
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Prevalence of Beta-Lactam and Quinolone/Fluoroquinolone Resistance in Enterobacteriaceae From Dogs in France and Spain—Characterization of ESBL/pAmpC Isolates Genes and Conjugative Plasmids

机译:法国和西班牙犬肠杆菌科中对β-内酰胺和喹诺酮/氟喹诺酮耐药的普遍性—ESBL / pAmpC分离物基因和结合质粒的特征

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摘要

Quantitative data on fecal shedding of antimicrobial-resistant bacteria are crucial to assess the risk of transmission from dogs to humans. Our first objective was to investigate the prevalence of quinolone/fluoroquinolone-resistant and beta-lactam-resistant Enterobacteriaceae in dogs in France and Spain. Due to the particular concern about possible transmission of extended-spectrum cephalosporin (ESC)-resistant isolates from dogs to their owners, we characterized the ESBL/pAmpC producers collected from dogs. Rectal swabs from 188 dogs, without signs of diarrhea and that had not received antimicrobials for 4 weeks before the study, were quantified for total and resistant Enterobacteriaceae on selective media alone or containing relevant antibiotic concentrations. Information that might explain antibiotic resistance was collected for each dog. Extended-spectrum cephalosporin-resistant isolates were subjected to bacterial species identification (API20E), genetic lineage characterization (MLST), ESBL/pAmpC genes identification (sequencing), and plasmid characterization (pMLST). Regarding beta-lactam resistance, amoxicillin- (AMX) and cefotaxime- (CTX) resistant Enterobacteriaceae were detected in 70 and 18% of the dogs, respectively, whereas for quinolone/fluoroquinolone-resistance, Nalidixic acid- (NAL) and ciprofloxacin- (CIP) resistant Enterobacteriaceae were detected in 36 and 18% of the dogs, respectively. Medical rather than preventive consultation was a risk marker for the presence of NAL and CIP resistance. CTX resistance was mainly due to a combination of specific ESBL/pAmpC genes and particular conjugative plasmids already identified in human patients: blaCTX−M−1/IncI1/ST3 (n = 4), blaCMY−2/IncI1/ST12 (n = 2), and blaCTX−M−15/IncI1/ST31 (n = 1). blaSHV−12 (n = 3) was detected in various plasmid lineages (InI1/ST3, IncI1/ST26, and IncFII). ESBL/pAmpC plasmids were located in different genetic lineages of E. coli, with the exception of two strains in France (ST6998) and two in Spain (ST602). Our study highlights dogs as a potential source of Q/FQ-resistant and ESBL/pAmpC-producing bacteria that might further disseminate to humans, and notably a serious risk of future acquisition of CTX-M-1 and CMY-2 plasmids by the owners of dogs.
机译:粪便中的抗微生物细菌的定量数据对于评估从狗传播给人类的风险至关重要。我们的首要目标是调查法国和西班牙犬中对喹诺酮/氟喹诺酮类耐药和对β-内酰胺类耐药的肠杆菌的患病率。由于对从狗向其所有者传播广谱头孢菌素(ESC)耐药菌株的可能特别关注,我们对从狗收集的ESBL / pAmpC生产者进行了鉴定。在研究前的4周内,对188只狗的直肠拭子进行了定量分析,它们仅在选择性培养基上或含有相关抗生素浓度时对总肠杆菌和耐药肠杆菌进行定量,这些肠拭子没有腹泻的迹象并且在4周内未接受任何抗生素治疗。为每只狗收集了可能解释抗生素抗性的信息。对广谱头孢菌素耐药菌株进行了细菌种类鉴定(API20E),遗传谱系鉴定(MLST),ESBL / pAmpC基因鉴定(测序)和质粒鉴定(pMLST)。关于β-内酰胺耐药性,分别在70%和18%的狗中检出了对阿莫西林-(AMX)和头孢噻肟-(CTX)耐药的肠杆菌科,而对于喹诺酮/氟喹诺酮耐药的狗,萘啶酸-(NAL)和环丙沙星-(分别在36%和18%的狗中检出了CIP)抵抗性肠杆菌科。医疗而不是预防性咨询是NAL和CIP耐药存在的风险标志。 CTX抗药性主要是由于特定的ESBL / pAmpC基因与已在人类患者中鉴定出的特定结合质粒的组合:blaCTX-M-1 / IncI1 / ST3(n = 4),blaCMY-2 / IncI1 / ST12(n = 2 )和blaCTX-M-15 / IncI1 / ST31(n = 1)。在各种质粒谱系(InI1 / ST3,IncI1 / ST26和IncFII)中检测到blaSHV-12(n = 3)。 ESBL / pAmpC质粒位于大肠杆菌的不同遗传谱系中,除了法国的两种菌株(ST6998)和西班牙的两种菌株(ST602)外。我们的研究强调,狗是Q / FQ抗药性和ESBL / pAmpC产生细菌的潜在来源,可能会进一步传播给人类,尤其是主人将来可能会收购CTX-M-1和CMY-2质粒狗。

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