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尼日利亚屠宰场和家禽来源的大肠杆菌、肺炎克雷伯菌和铜绿假单胞菌分离株中的金属β-内酰胺酶和 AmpC 基因。

Metallo-β-lactamase and AmpC genes in Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa isolates from abattoir and poultry origin in Nigeria.

机构信息

Department of Applied Microbiology, Ebonyi State University, Abakaliki, Nigeria.

Department of Biological Sciences, Alex Ekwueme Federal University, Ndufu-Alike Ikwo, Ikwo, Nigeria.

出版信息

BMC Microbiol. 2021 Apr 21;21(1):124. doi: 10.1186/s12866-021-02179-1.

Abstract

BACKGROUND

Gram-negative bacteria (GNB) including Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae represent the most relevant reservoir of resistance genes such as metallo-β-lactamase (MBL) and AmpC genes that give them the undue advantage to resist antimicrobial onslaught. This study aimed to investigate the occurrence of MBL (bla, bla, bla, bla) and AmpC (bla, bla, bla, bla) resistance genes in aforementioned GNB collected from abattoir and poultry sources in Nigeria.

RESULTS

In total, 370 isolates were collected from abattoir tables (n = 130), anal region of cows (n = 120), and the cloacae of poultry birds (n = 120). The test isolates showed high rate of resistance to cephalosporins and carbapenems. The MBLs were phenotypically detected in 22 E. coli, 22 P. aeruginosa, and 18 K. pneumoniae isolates using combined disc test (CDT). However, only 11 E. coli, 24 P. aeruginosa, and 18 Klebsiella pneumoniae isolates were phenotypically confirmed to be AmpC producers using cefoxitin-cloxacillin double disk synergy test (CC-DDST). MBL encoding genes (particularly the bla genes and bla genes) were detected by polymerase chain reaction (PCR) in 12 (54.6%) E. coli, 15 (83.3%) K. pneumoniae, and 16 (72.7%) P. aeruginosa isolates. AmpC genes (particularly the bla genes and bla genes) were found in a total of 5 (29.4%) E. coli isolates, 5 (27.8%) isolates of K. pneumoniae, and 10 (41.7%) isolates of P. aeruginosa.

CONCLUSIONS

Our study showed the circulation of MBL and AmpC genes in GNB from abattoir and poultry origin in Nigeria. Adoption of regular control policies is necessary to reduce the spread of these species as soon as possible, especially in poultry and slaughterhouses.

摘要

背景

革兰氏阴性菌(GNB)包括大肠杆菌、铜绿假单胞菌和肺炎克雷伯菌,它们是金属β-内酰胺酶(MBL)和 AmpC 基因等耐药基因的最重要储存库,使它们具有过度的优势来抵抗抗菌药物的攻击。本研究旨在调查来自尼日利亚屠宰场和家禽来源的上述 GNB 中 MBL(bla、bla、bla、bla)和 AmpC(bla、bla、bla、bla)耐药基因的发生情况。

结果

总共从屠宰场案板(n=130)、牛肛门区域(n=120)和禽鸟泄殖腔(n=120)收集了 370 株分离株。这些受试分离株对头孢菌素和碳青霉烯类药物的耐药率很高。使用联合纸片试验(CDT)在 22 株大肠杆菌、22 株铜绿假单胞菌和 18 株肺炎克雷伯菌分离株中检测到 MBL 表型。然而,仅通过头孢西丁-克拉维酸双碟协同试验(CC-DDST)在 11 株大肠杆菌、24 株铜绿假单胞菌和 18 株肺炎克雷伯菌分离株中表型确认 AmpC 产生菌。聚合酶链反应(PCR)检测到 12 株(54.6%)大肠杆菌、15 株(83.3%)肺炎克雷伯菌和 16 株(72.7%)铜绿假单胞菌分离株中存在 MBL 编码基因(特别是 bla 基因和 bla 基因)。总共在 5 株(29.4%)大肠杆菌分离株、5 株(27.8%)肺炎克雷伯菌分离株和 10 株(41.7%)铜绿假单胞菌分离株中发现 AmpC 基因(特别是 bla 基因和 bla 基因)。

结论

本研究表明,尼日利亚屠宰场和家禽来源的 GNB 中存在 MBL 和 AmpC 基因。需要采取定期的控制政策来减少这些物种的传播,特别是在禽鸟和屠宰场。

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