蛋鸡弯曲杆菌SPP分子检测分离方法及耐药模式研究

O. Kehinde, M. Dipeolu, O. Awoyomi, M. Agbaje, O. Fasanmi, I. Kassem, O. Ojo, O. Adebowale, E. Omoshaba, J. Nwanta
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引用次数: 0

摘要

本研究比较了两种从商品蛋鸡中分离弯曲杆菌的培养方法,并采用聚合酶链反应(PCR)对其进行了验证。此外,还测定了PCR阳性弯曲杆菌分离株的耐药谱。从奥贡州4个地理区域的5个家禽养殖场随机选取550只鸡,采用改性炭Cefoperazone脱氧胆酸琼脂(MCCDA)和改进的培养方法(Preston肉汤预富集,随后在添加弯曲杆菌生长添加剂的Mueller Hinton琼脂上进行传代培养)对其进行肠粘膜菌签培养。随后通过PCR和测序分析证实了假定的分离株。其他在MCCDA上生长并经测序分析证实的分离株有粪肠球菌、大肠杆菌、克氏单胞菌和风产假单胞菌。采用多重聚合酶链反应(mPCR)对所有菌株的四环素类(tetO)、多类(cmeB)、氨基糖苷类(aphA-3-1)和β-内酰胺类(Blaoxa-61)耐药基因进行基因典型分析,采用微肉汤稀释法对与耐药基因对应的氯霉素、泰霉素、链霉素、环丙沙星和红霉素耐药基因进行表型分析。MCCDA检测显示弯曲杆菌的表观流行率为16.8%,而PCR检测均为阴性。同时,用Preston肉汤预富集和Mueller Hinton琼脂培养基添加弯曲杆菌生长物,得到的感染率为26%,其中11/50(22%)的分离株经PCR证实为阳性。PCR阳性菌株的基因型鉴定结果显示,10/11(90%)为大肠杆菌,1/11(10%)为其他弯曲杆菌,0%为空肠杆菌。所有分离株均携带tetO和cmeB耐药基因。最低抑菌浓度结果显示,所有PCR阳性菌株对四环素、环丙沙星、红霉素、大观霉素和泰乐素的耐药率分别为10/10(100%)、9/10(90%)、6/10(60%)、9/10(90%)和8/10(80%)。此外,所有分离株都对尼日利亚家禽实践中常用的大多数抗生素具有多重耐药性。研究区弯曲杆菌表现出多样的基因型特征,并有基因介导的多药耐药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ISOLATION METHODS FOR MOLECULAR DETECTION AND ANTIBIOTIC RESISTANCE PATTERN OF CAMPYLOBACTER SPP IN LAYER CHICKENS
This study was conducted to compare two culture methods for the isolation of Campylobacter spp from commercial layer chickens and subsequently confirmed by Polymerase Chain Reaction assays (PCR). Furthermore, the antimicrobial resistance profiles of PCR positive Campylobacter isolates were determined.Cloacal swab samples (550) from chickens randomly selected from five poultry farms in the four geographical zones in Ogun State were cultured for Campylobacter using modified charcoal Cefoperazone deoxycholate agar (MCCDA) and an improved culture method involving Preston broth pre-enrichment and subsequent subculture on Mueller Hinton agar with Campylobacter growth supplements. Putative isolates were later confirmed by PCR assay and sequencing analysis.Other isolates that grew on MCCDA and confirmed by sequencing analysis are Enterococcus faecalis, Escherichis coli, Comamonas kerstli and Pseudomonas aeroginusa . The antibiotic resistant profile of all the isolates were evaluated genotypically for resistance genes to tetracyclines (tetO), multiclasses (cmeB), aminoglycosides (aphA-3-1) and β-lactams (Blaoxa-61) using multiplex PCR (mPCR), and phenotypically for chlortetracycline, tylosin, streptomycin, ciprofloxacin and erythromycin resistance by microbroth dilution method which correspond to the antibiotic resistance genes. The apparent prevalence of Campylobacter was 16.8% by MCCDA while none of the isolates was positive to PCR. Meanwhile, prevalence rate of 26% was obtained using Preston broth pre-enrichment and Mueller Hinton agar with Campylobacter growth supplements, of which 11/50 (22%) of the isolates was confirmed positive by PCR. Genotypic characterization of PCR positive isolates showed 10/11(90%) were C. coli, 1/11(10%) other Campylobacter species and 0% C. jejuni. All the isolates carried both tetO and cmeB resistant genes. The results of minimum inhibitory concentration presented all PCR positive isolates had resistance of 10/10(100%), 9/10(90%), 6/10(60%), 9/10(90%), and 8/10(80%) to tetracycline, ciprofloxacin, erythromycin, spectinomycin and tylosin respectively. In addition, all isolates carried multiple resistance to most antibiotics tested which are commonly used in poultry practice in Nigeria. Campylobacter spp in the study areas showed diverse genotypic characteristics, and gene mediated multidrug resistance.    
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