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Identification and molecular typing of Streptococcus agalactiae isolated from pond-cultured tilapia in China

机译:中国池塘养殖罗非鱼无乳链球菌的鉴定和分子分型

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Bacteria strains with strong virulence were isolated from pond-cultured tilapia in China. They were identified as Streptococcus agalactiae by biochemical assays, and confirmed by 16S ribosomal RNA (rRNA) and group?B Streptococcus (GBS)-specific gene cfb analyses. Multiplex polymerase chain reaction (PCR) assay of the alpha?C protein (ACP) gene and capsular polysaccharide antigen (cps) gene was employed to identify their molecular serotype (MS). Amplification of the ACP gene produced a 400-bp C alpha protein gene (bca) fragment, suggesting that these isolates belong to MS Ia, Ib or II; amplification of cps produced a 790-bp amplicon, indicating that they belong to MS Ia/III-3. An additional PCR based on nucleotide difference in the cps H–I region of MS Ia and III further suggested that the isolates belong to serotype MS Ia. Moreover, multi-locus sequence typing (MLST) indicated that these strains were of sequence type?7 (ST-7). These results showed that isolates from different regions of China shared the same MS and ST. However, none of the isolated ST-7 GBS corresponded to the capsular serotype, suggesting that these fish GBS possessed specific molecular characteristics not present in human or other animals. Data from this study will facilitate the understanding of epidemiology and nosogenesis of tilapia GBS and the establishment of effective disease prevention methods.
机译:从中国池塘养殖的罗非鱼中分离出具有强毒力的细菌菌株。通过生化分析将其鉴定为无乳链球菌,并通过16S核糖体RNA(rRNA)和B组链球菌(GBS)特异性基因cfb分析加以证实。用α?C蛋白(ACP)基因和荚膜多糖抗原(cps)基因的多重聚合酶链反应(PCR)法鉴定其分子血清型(MS)。 ACP基因的扩增产生了一个400 bp的Cα蛋白基因(bca)片段,这表明这些分离物属于MS Ia,Ib或II。 cps的扩增产生了790bp的扩增子,表明它们属于MS Ia / III-3。基于MS Ia和III的cps H–I区核苷酸差异的另一种PCR进一步表明,分离株属于血清型MS Ia。此外,多位点序列分型(MLST)表明这些菌株的序列类型为α7(ST-7)。这些结果表明,来自中国不同地区的分离株具有相同的MS和ST。但是,分离出的ST-7 GBS均没有对应于荚膜的血清型,表明这些鱼类GBS具有人类或其他动物所不具备的特定分子特征。这项研究的数据将有助于了解罗非鱼GBS的流行病学和致病机理,并建立有效的疾病预防方法。

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