畜牧与饲料科学 ›› 2024, Vol. 45 ›› Issue (1): 114-119.doi: 10.12160/j.issn.1672-5190.2024.01.017

• 动物疾病防控 • 上一篇    下一篇

新疆维吾尔自治区阿拉尔市某规模化养殖场猪乳源金黄色葡萄球菌的分离鉴定及其毒力、耐药性分析

陈俊凯, 于月通, 杨彬, 王泽坤, 李静, 陀海欣, 徐俊飞, 齐萌   

  1. 塔里木大学动物科学与技术学院/新疆生产建设兵团塔里木动物疫病诊断与防控工程实验室,新疆 阿拉尔 843300
  • 收稿日期:2024-01-17 出版日期:2024-01-30 发布日期:2024-03-14
  • 通讯作者: 齐萌(1985—),男,教授,博士,硕士生导师,主要从事人兽共患病病原生物学研究工作。
  • 作者简介:陈俊凯(1996—),男,硕士研究生,主要研究方向为动物群发病防治。
  • 基金资助:
    新疆生产建设兵团重点领域科技攻关计划项目(2020AB025)

Isolation,Identification and Characterization of Virulence and Antimicrobial Resistance of Staphylococcus aureus Strains from Porcine Milk in a Large-scale Farm in Aral City,Xinjiang Uygur Autonomous Region

CHEN Junkai, YU Yuetong, YANG Bin, WANG Zekun, LI Jing, TUO Haixin, XU Junfei, QI Meng   

  1. College of Animal Science and Technology,Tarim University/Engineering Laboratory of Tarim Animal Diseases Diagnosis and Control,Xinjiang Production and Construction Corps,Aral 843300,China
  • Received:2024-01-17 Online:2024-01-30 Published:2024-03-14

摘要: [目的]分离鉴定新疆维吾尔自治区阿拉尔市猪乳源金黄色葡萄球菌,了解其致病性和耐药性。[方法]从阿拉尔市某规模化养殖场收集6份新鲜猪乳样本,采用甘露醇高盐琼脂(MSA)培养基分离乳样中的金黄色葡萄球菌,利用表型鉴定方法及细菌16S rDNA序列分析法对分离到的菌株进行鉴定,检测分离菌株的生物被膜形成能力,利用K-B纸片扩散法进行药物敏感性试验,利用PCR法检测毒力基因和耐药基因。[结果]经分离培养及分子生物学鉴定,从6份乳样中获得2株金黄色葡萄球菌,分离率为33.33%(2/6);2株金黄色葡萄球菌均具有强生物被膜形成能力(+++);2株金黄色葡萄球菌均对利福平敏感,均对青霉素、头孢西丁、四环素、红霉素、替米考星、克林霉素和磺胺甲噁唑耐药;在检测的5种耐药基因中,2株金黄色葡萄球菌均携带ant(4)基因和mecA基因;在检测的20种毒力基因中,共检测到6种毒力基因,其中,2株金黄色葡萄球菌均携带segseihlbfnbAclfA基因,有1株携带hla基因。[结论]该养殖场猪乳源金黄色葡萄球菌生物被膜形成能力强,携带多种毒力基因和耐药基因,表现为多重耐药性。

关键词: 金黄色葡萄球菌, 分离, 鉴定, 致病性, 耐药性, 猪乳

Abstract: [Objective] The aims of the present study were to isolate and identify Staphylococcus aureusS. aureus) strains from porcine milk in Aral City, Xinjiang Uygur Autonomous Region, and to characterize the virulence and antimicrobial resistance of the isolates.[Method] Six fresh porcine milk samples were collected from a large-scale farm in Aral City, and mannitol salt agar (MSA) was used to isolate S. aureus strains. The isolates were confirmed by phenotypic identification method and 16S rDNA sequence analysis. The biofilm formation ability of the isolates was determined. Antimicrobial sensitivity test was performed using K-B disk diffusion method. PCR assay was employed to detect the virulence and antimicrobial resistance genes.[Result]After isolation and molecular biology identification, two S. aureus strains were obtained from the milk samples, with a separation rate of 33.33% (2/6). Both isolates had strong biofilm formation ability (+++). The two isolates were sensitive to rifampicin and resistant to penicillin, cefoxitin, tetracycline, erythromycin, temicoxacin, clindamycin and sulfamethoxazole. Out of the five tested antimicrobial resistance genes, both isolates carried ant (4) gene and mecA gene. A total of six virulence genes were detected among the twenty tested virulence genes. Among these, both isolates carried seg, sei, hlb, fnbA and clfA genes. One isolate carried hla gene.[Conclusion]The porcine milk derived S. aureus strains in this farm had strong biofilm formation ability and carried multiple virulence and antimicrobial resistance genes, exhibiting multiple-drug resistance.

Key words: Staphylococcus aureus, isolation, identification, virulence, antimicrobial resistance, porcine milk

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