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7型猪链球菌的分离鉴定和特性研究

Isolation, Identification and Characterization of Streptococcus Suis Serotype 7

中文摘要英文摘要

通过生化鉴定,PCR鉴定的方法从湖北省部分地区高热症病料中分离鉴定17株7型猪链球菌,并对所分离菌株进行药敏,毒力基因分布,致病性等生活学特性的研究。结果表明,生化鉴定显示所分离菌株为猪链球菌2型,但经PCR鉴定为7型,测序结果经分析与已发表序列同源性为100%。17株7型分离株毒力基因分布情况为:0.0%为mrp+, 11.8%为epf+, 17.6%为sly+orf2+, 29.4%fbps+, 100.0%gdh+。通过对28种药物的敏感试验发现各分离株耐药性差别很大,但对阿莫西林和复方阿莫西林较为敏感(88.2%),对红霉素最为敏感(100.0%)。动物试验表明编号为HB6、HB8、HB9的分离株致病性较强。通过对病猪和感染小鼠进行病理切片观察,各器官充血出血最为明显。总之,在以高致病性蓝耳病病毒为主要病原的高热症诊断和治疗中,同样需要考虑混合或继发感染7型猪链球菌的致病作用。

17 isolates of Streptococcus suis serotype 7 from diseased pigs with "High Fever Syndrome" in Hubei province, China, were characterized by automatic biochemical identification, PCR typing, antimicrobial susceptibility testing, PCR test of virulence gene, animal test assay and pathobiology. The results of automatic biochemistry identification indicated that all isolates belonged to serotype 2, but serotype 7 by PCR typing. Sequence homology of all strains was 100% as sequences reported The distribution of virulence gene test showed that mrp+ (0.0%), epf+(11.8%), sly+orf2+(17.6%), fbps+(29.4%), gdh+(100.0%) of 17 serotype 7 strains. Antimicrobial susceptibility of all test strains to 28 antimicrobial agents were very different, but 15(88.2%) strains were resistance to amoxicillin , compound amoxicillin respectively and 17(100%) strains were susceptible to erythromycin. Result of mouse virulence test showed that virulence of strain HB6, strain HB8, strain HB9 was highly than others. In histopathology, congestion and hemorrhage of main organs of diseased pigs and infection mice were obvious in this research. In conclusion, S.suis serotype 7 had existed in Hubei province and there was polyinfection of serotype 7 in pigs with "high fever syndrome" whose mainly pathogen was PRRSV.

胡智斌、江甜、谷长勤、宋念华、张万坡、程国富、胡薛英

微生物学基础医学医学研究方法

7型猪链球菌鉴定生物学特性

Streptococcus suis serotype 7IdentificationBiological Characterization

胡智斌,江甜,谷长勤,宋念华,张万坡,程国富,胡薛英.7型猪链球菌的分离鉴定和特性研究[EB/OL].(2011-01-17)[2025-08-18].http://www.paper.edu.cn/releasepaper/content/201101-828.点此复制

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