水产科学
水產科學
수산과학
FISHERIES SCIENCE
2014年
12期
791-799
,共9页
王蓓%黎源%陈贺%李桂欢%鲁义善%汤菊芬%蔡佳%吴灶和%简纪常
王蓓%黎源%陳賀%李桂歡%魯義善%湯菊芬%蔡佳%吳竈和%簡紀常
왕배%려원%진하%리계환%로의선%탕국분%채가%오조화%간기상
无乳链球菌%16S rRNA基因%多位点序列分析%分子流行病学
無乳鏈毬菌%16S rRNA基因%多位點序列分析%分子流行病學
무유련구균%16S rRNA기인%다위점서렬분석%분자류행병학
Streptococcus agalactiae%16S rRNA gene%multilocus sequence typing%molecular epidemiolo-gy
为了解我国3个地区(广东省、广西省和海南省)罗非鱼源无乳链球菌临床株的遗传背景及进化关系,对2010—2011年间采集分离的128株链球菌,采用Bio‐MerieuxVITEK进行生理生化分析和16S rRNA法鉴定菌株类型,并运用多位点序列分型技术,确定其等位基因谱型及菌株序列型。试验结果表明,通过对分离菌株的生理生化及16S rRNA 基因进行分析,确认有104株为无乳链球菌,这104株分属1个已知克隆系ST‐7和2个未知克隆系NST‐1和NST‐2,其中NST‐1克隆系所占比列最多,占88.5%(92/104)。本研究结果揭示了我国南方3个地区无乳链球菌分离株呈多克隆系并存,以新型NST‐1克隆系为主,应加强对新克隆系的病原学监测。应用MLST 分子分型技术,初步揭示了我国南方3个地区罗非鱼源无乳链球菌的遗传进化关系。
為瞭解我國3箇地區(廣東省、廣西省和海南省)囉非魚源無乳鏈毬菌臨床株的遺傳揹景及進化關繫,對2010—2011年間採集分離的128株鏈毬菌,採用Bio‐MerieuxVITEK進行生理生化分析和16S rRNA法鑒定菌株類型,併運用多位點序列分型技術,確定其等位基因譜型及菌株序列型。試驗結果錶明,通過對分離菌株的生理生化及16S rRNA 基因進行分析,確認有104株為無乳鏈毬菌,這104株分屬1箇已知剋隆繫ST‐7和2箇未知剋隆繫NST‐1和NST‐2,其中NST‐1剋隆繫所佔比列最多,佔88.5%(92/104)。本研究結果揭示瞭我國南方3箇地區無乳鏈毬菌分離株呈多剋隆繫併存,以新型NST‐1剋隆繫為主,應加彊對新剋隆繫的病原學鑑測。應用MLST 分子分型技術,初步揭示瞭我國南方3箇地區囉非魚源無乳鏈毬菌的遺傳進化關繫。
위료해아국3개지구(광동성、광서성화해남성)라비어원무유련구균림상주적유전배경급진화관계,대2010—2011년간채집분리적128주련구균,채용Bio‐MerieuxVITEK진행생리생화분석화16S rRNA법감정균주류형,병운용다위점서렬분형기술,학정기등위기인보형급균주서렬형。시험결과표명,통과대분리균주적생리생화급16S rRNA 기인진행분석,학인유104주위무유련구균,저104주분속1개이지극륭계ST‐7화2개미지극륭계NST‐1화NST‐2,기중NST‐1극륭계소점비렬최다,점88.5%(92/104)。본연구결과게시료아국남방3개지구무유련구균분리주정다극륭계병존,이신형NST‐1극륭계위주,응가강대신극륭계적병원학감측。응용MLST 분자분형기술,초보게시료아국남방3개지구라비어원무유련구균적유전진화관계。
Identification was carried out in 128 strains of Streptococcus isolated from tilapia in southern China (Guangdong ,Guangxi and Hainan provinces ) from 2010 to 2011 by Bio‐MerieuxVITEK and 16S rRNA sequence analysis and 7 housekeeping genes were seguenced in 104 strains of S .agalactiae by Mul‐tilocus Sequence Typing (MLST ) technique to evaluate the genetic diversity of S . agalactiae .Results were analyzed and compared with sequence information in PubMLST databases to determine a strain allelic profile and assigned a sequence type (ST ) .It was found that total 104 strains were within 3 clone se‐quences :ST‐7 and 2 types of unidentified NST‐1 and NST‐2 ,NST‐1 having the maximal proportion of 88 .5% (92/104) .It was revealed that there were multiple clonal sequences of S .agalactiae isolate from tilapia in southern China with high pathogenetic and prevalent .It is suggested that S . agalactiae isolate from tilapia be intense surveillance efforts .The findings indicate that MLST technique is an ideal tool to reveal genetic evolution profile of S .agalactiae isolated from tilapia in southern China .