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Detection and molecular typing of Streptococcus suis in tonsils from live pigs in France

机译:法国活猪扁桃体中猪链球菌的检测和分子分型

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Streptococcus suis is an important pathogen of swine, causing meningitis, arthritis, polyserositis, septicemia, and sudden death in weaning piglets as well as fattening pigs. Recently, 3 molecular tests have been developed in our laboratory: a multiplex polymerase chain reaction (m-PCR) assay for the detection of S. suis species and serotypes 2 and 1/2, and 2 molecular typing methods, pulsed-field gel electrophoresis and an approach based on PCR amplification of a fragment of rRNA genes, including a part of the 16S and 23S genes and the 16S–23S rDNA intergenic spacer region (ISR), followed by restriction fragment length polymorphism (RFLP) analysis (ISR-RFLP). In the present study, we used these tests to analyze tonsil samples from clinically healthy pigs and to identify individual isolates of S. suis during epidemiologic investigations of 8 related herds with a history of septicemia caused by S. suis serotype 2. Capsular typing showed that 58% of the strains were nontypable. Of the 17 serotypes present, serotype 22 was the most prevalent. In the 7 farms without clinical signs on the day of sampling, we detected S. suis serotype 2 or 1/2, or both, in less than 5% of the pigs by m-PCR or by bacteriologic culture. In the 8th farm, on which 2 pigs had clinical signs of septicemia on the day of sampling, we detected S. suis serotype 2 or 1/2, or both, by m-PCR in the tonsils of 40% of fattening pigs (21 wk old) that lacked symptoms. Molecular typing of the serotype 2 strains showed a common origin of contamination in these herds, given that 1 pattern (C1) was detected in the isolates from 6 of the 8 herds. However, up to 4 patterns were associated with septicemia and sudden death. Several patterns of S. suis serotype 2 can be responsible for disease in the same herd. These molecular tools may be useful for confident studies of the transmission of S. suis, thereby contributing to the control of S. suis infection.
机译:猪链球菌是猪的重要病原体,在断奶仔猪和育肥猪中引起脑膜炎,关节炎,多发性浆膜炎,败血病和猝死。最近,我们实验室已开发出3种分子测试方法:用于检测猪链球菌物种和血清型2和1/2的多重聚合酶链反应(m-PCR)分析,以及2种分子分型方法,脉冲场凝胶电泳一种基于PCR扩增rRNA基因片段的方法,包括部分16S和23S基因以及16S-23S rDNA基因间隔区(ISR),然后进行限制性片段长度多态性(RFLP)分析(ISR-RFLP )。在本研究中,我们使用这些测试来分析临床上健康的猪的扁桃体样本,并在对8例由猪链球菌2型引起败血症的相关猪群进行流行病学调查期间,确定猪链球菌的分离株。 58%的菌株是不可分型的。在目前存在的17种血清型中,血清型22最流行。在抽样当天,在没有临床症状的7个农场中,我们通过m-PCR或细菌培养在不到5%的猪中检测到了猪链球菌血清型2或1/2,或两者都有。在第8个猪场中,当天有2头猪有败血症的临床征象,我们通过m-PCR在40%育肥猪的扁桃体中检测到了猪链球菌2型或1/2型或两者。 wk old)缺乏症状。血清型2菌株的分子分型显示了这些畜群中常见的污染源,因为从8个畜群中有6个分离物中检测到1种模式(C1)。但是,多达4种模式与败血病和猝死有关。猪链球菌血清型2的几种模式可导致同一群猪的疾病。这些分子工具可用于可靠地研究猪链球菌的传播,从而有助于控制猪链球菌的感染。

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