Suppr超能文献

用于鉴定猪链球菌近亲——副猪链球菌的聚合酶链反应(PCR)技术的开发。

Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis.

作者信息

Yamada Ryoko, Tien Le Hong Thuy, Arai Sakura, Tohya Mari, Ishida-Kuroki Kasumi, Nomoto Ryohei, Kim Hyunjung, Suzuki Eriko, Osawa Ro, Watanabe Takayasu, Sekizaki Tsutomu

机构信息

Research Center for Food Safety, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan.

Present address: Laboratory of Veterinary Ethology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

J Vet Med Sci. 2018 Jul 12;80(7):1101-1107. doi: 10.1292/jvms.18-0083. Epub 2018 Jun 6.

Abstract

Streptococcus parasuis has recently been removed taxonomically from Streptococcus suis, a zoonotic pathogen. S. parasuis has been detected in healthy pigs and in diseased pigs, which suggests that S. parasuis is involved in the normal microbiota of pigs and has potential pathogenicity. However, the pathogenicity of S. parasuis in pigs is unclear because of the lack of appropriate detection methods that discriminate S. parasuis from S. suis. In this study, we developed a PCR method that is specific for S. parasuis. The detection limit of the PCR was 350 CFU per reaction. Bacteria isolated from the saliva of eight pigs were collected and examined by PCR. Sixty-four isolates positive for PCR were obtained from the samples of all pigs. Thirteen of the 64 isolates were genetically confirmed as S. parasuis, and biologically and biochemically had nearly the same features of known S. parasuis strains, which suggested that strains positive for PCR were S. parasuis. Among the 64 isolates, 28 isolates were serotypes 20, 22, or 26 in the S. suis serotyping scheme. The remaining 36 isolates were untypeable, which suggested the presence of novel serotypes or a capsule-negative form. Therefore, the PCR method described in this study is a useful tool for identifying S. parasuis, and can be used in etiological studies on this bacterium.

摘要

副猪链球菌最近已从人畜共患病原体猪链球菌中进行了分类学上的分离。副猪链球菌已在健康猪和患病猪中被检测到,这表明副猪链球菌参与了猪的正常微生物群,并且具有潜在致病性。然而,由于缺乏将副猪链球菌与猪链球菌区分开来的适当检测方法,副猪链球菌在猪中的致病性尚不清楚。在本研究中,我们开发了一种针对副猪链球菌的PCR方法。该PCR的检测限为每个反应350 CFU。收集了从8头猪的唾液中分离出的细菌,并通过PCR进行检测。从所有猪的样本中获得了64株PCR阳性分离株。64株分离株中有13株经基因鉴定为副猪链球菌,其生物学和生化特征与已知的副猪链球菌菌株几乎相同,这表明PCR阳性菌株为副猪链球菌。在这64株分离株中,有28株在猪链球菌血清分型方案中属于20、22或26型。其余36株无法分型,这表明存在新的血清型或无荚膜形式。因此,本研究中描述的PCR方法是鉴定副猪链球菌的有用工具,可用于该细菌的病因学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fea0/6068303/0ddea060866f/jvms-80-1101-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验