Molecular Detection of Virulence Genes and Multi-drug Resistance Patterns in Streptococcus Agalactiae in Clinical Bovine Mastitis: Tehran and Alborz Provinces, Iran.

Q3 Veterinary
Hashemi Haghighi Fatemeh, Pourtaghi Hadi, Harzandi Naser, Moosakhani Farhad
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引用次数: 0

Abstract

Introduction: Streptococcus agalactiae is one of the important causes of mastitis in cows. The ability of S. agalactiae to cause disease depends on the production of a large number of virulence factors encoded by different genes. The overuse of antibiotics to treat mastitis can lead to antibiotic resistance. This research was conducted to detect selected virulence genes and assess the antibiotic resistance of S. agalactiae.

Materials & methods: A total of 30 bacteria that isolated from clinical cases of mastitis and characterized as S. agalactiae by conventional cultural methods was collected from veterinary diagnostic laboratories. Then, these isolates undergo further characterization by detecting virulence genes by molecular methods and antibiotic resistance by disc diffusion method.

Results: Of these, 24 samples were confirmed as S. agalactiae through the detection of the two 16S-23S rRNA genes. The disk diffusion method, using a panel of 10 antimicrobial agents, showed a large number of strains resistant simultaneously to six antibiotics. Five virulence genes bac, bca, cylE, hylB, and cfb were screened by polymerase chain reaction (PCR). The cfb and hylB genes were found in 95.83 % of the isolates,while the cylE gene was detected in 29.16% of the isolates. The bca and bac genes were not detected in any of the isolates. The absence of bac and bca genes suggests that they likely have minimal impact on the pathogenesis of S. agalactiae mastitis in dairy cows, while the hylB and cfb genes play a crucial role in this condition.

Conclusion: The results presented here are one of the first molecular data concerning these five virulence genes in S. agalactiae isolates causing bovine mastitis in the Tehran and Alborz provinces, providing a foundation for the development of diagnostic, preventive, and therapeutic methods.

临床牛乳腺炎无乳链球菌毒力基因和多重耐药模式的分子检测:伊朗德黑兰和阿尔博尔兹省。
简介:无乳链球菌是奶牛乳腺炎的重要病因之一。无乳链球菌致病的能力取决于由不同基因编码的大量毒力因子的产生。过度使用抗生素治疗乳腺炎可导致抗生素耐药性。本研究旨在检测选定的毒力基因并评估无乳链球菌的耐药性。材料与方法:从兽医诊断实验室采集临床乳腺炎病例中分离到的经常规培养鉴定为无乳链球菌的细菌30株。然后,通过分子方法检测毒力基因,通过圆盘扩散法检测抗生素耐药性,对这些分离物进行进一步的鉴定。结果:其中24份样品通过16S-23S rRNA基因检测确认为无乳链球菌。使用10种抗菌药物的圆盘扩散法显示,大量菌株同时对6种抗生素耐药。采用聚合酶链反应(PCR)技术筛选了5个毒力基因bac、bca、cycle、hylB和cfb。cfb和hylB基因检出率为95.83%,cycle基因检出率为29.16%。在所有分离株中均未检测到bca和bac基因。bac和bca基因的缺失表明它们可能对奶牛无乳链球菌性乳腺炎的发病机制影响很小,而hylB和cfb基因在这种情况下起着至关重要的作用。结论:本文的研究结果是德黑兰和Alborz省无乳链球菌分离株中这五个毒力基因的首次分子数据之一,为发展诊断、预防和治疗方法提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of Razi Institute
Archives of Razi Institute Veterinary-Veterinary (all)
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
12 weeks
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