中国人兽共患病学报
中國人獸共患病學報
중국인수공환병학보
CHINESE JOURNAL OF ZOONOSES
2010年
1期
62-64
,共3页
姚苹苹%王复甦%朱函坪%梅玲玲%叶菊连%罗进%张政%姚晨辉
姚蘋蘋%王複甦%硃函坪%梅玲玲%葉菊連%囉進%張政%姚晨輝
요평평%왕복소%주함평%매령령%협국련%라진%장정%요신휘
猪链球菌2型%Cps2J基因%序列分析
豬鏈毬菌2型%Cps2J基因%序列分析
저련구균2형%Cps2J기인%서렬분석
Streptococcus suis serotype 2%Cps2Jgene%sequence analyses
目的 了解浙江猪链球菌2型(SS2)分离株的分子基础及与国内外其他分离株的基因差异程度,确定Cps2J基因变异位点和频率,为该地区的猪链球菌防治提供科学依据.方法 提取菌株DNA,应用聚合酶链反应(PCR)扩增菌株Cps2J基因全片段,克隆入质粒载体,纯化后采用ABI自动测序仪测定序列,并同国内外其他分离株的基因进行比较.结果 扩增出9株菌株的Cps2J基因的完整开放阅读框(ORF)都为999bp,编码333个氨基酸,9株菌株Cps2J片段核苷酸高度同源,同源性在99.7%~100%;与国内外其他的SS2核苷酸的同源性为98.8%~99.0%,与猪链球菌1型的同源性只有56.8%~57.0%. 结论 9株浙江省猪链球菌2型分离株Cps2J基因序列非常保守,这些不同来源的菌株可能有相同的起源.
目的 瞭解浙江豬鏈毬菌2型(SS2)分離株的分子基礎及與國內外其他分離株的基因差異程度,確定Cps2J基因變異位點和頻率,為該地區的豬鏈毬菌防治提供科學依據.方法 提取菌株DNA,應用聚閤酶鏈反應(PCR)擴增菌株Cps2J基因全片段,剋隆入質粒載體,純化後採用ABI自動測序儀測定序列,併同國內外其他分離株的基因進行比較.結果 擴增齣9株菌株的Cps2J基因的完整開放閱讀框(ORF)都為999bp,編碼333箇氨基痠,9株菌株Cps2J片段覈苷痠高度同源,同源性在99.7%~100%;與國內外其他的SS2覈苷痠的同源性為98.8%~99.0%,與豬鏈毬菌1型的同源性隻有56.8%~57.0%. 結論 9株浙江省豬鏈毬菌2型分離株Cps2J基因序列非常保守,這些不同來源的菌株可能有相同的起源.
목적 료해절강저련구균2형(SS2)분리주적분자기출급여국내외기타분리주적기인차이정도,학정Cps2J기인변이위점화빈솔,위해지구적저련구균방치제공과학의거.방법 제취균주DNA,응용취합매련반응(PCR)확증균주Cps2J기인전편단,극륭입질립재체,순화후채용ABI자동측서의측정서렬,병동국내외기타분리주적기인진행비교.결과 확증출9주균주적Cps2J기인적완정개방열독광(ORF)도위999bp,편마333개안기산,9주균주Cps2J편단핵감산고도동원,동원성재99.7%~100%;여국내외기타적SS2핵감산적동원성위98.8%~99.0%,여저련구균1형적동원성지유56.8%~57.0%. 결론 9주절강성저련구균2형분리주Cps2J기인서렬비상보수,저사불동래원적균주가능유상동적기원.
To explore the molecular characteristics of Streptococcus suis serotype 2(ss2) isolated in Zhejiang province by deciding the variation loci and its variation frequency of Cps2J gene.The total DNA of 9 strains of ss2 isolated in Zhejiang province were extracted and amplifed by PCR. Then,the Cps2J fragments were cloned into plasmid carrier and completely sequenced after purification.Finally,the sequence results of all 9 ss2 isolates were compared with those obtained by other studies around the world.It was found that the open reading fragments of Cps2J in 9 SS2 isolates encoding 333 amino acids were 999 bp in length.Comparisons of this region among ss2 isolates revealed a similarity of between 98.8% and 99.9%, while the homology to ss1 strains varied between 56.8% and 57.0%.Our study shows the sequences of complete Cps2J segment are fairly stable and all these 9 ss2 strains of different sources possibly have the same evolutionary origin.