中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2014年
5期
388-392
,共5页
白巍%陈俊英%潘玥%朱艳菊%邵聪文%刘建生%马绍辉
白巍%陳俊英%潘玥%硃豔菊%邵聰文%劉建生%馬紹輝
백외%진준영%반모%주염국%소총문%류건생%마소휘
Echo30%全基因序列%序列分析
Echo30%全基因序列%序列分析
Echo30%전기인서렬%서렬분석
Echovirus 30%Complete genome%Sequence analysis
目的:对2009年从中国云南省1名脑炎患儿粪便标本中分离到的Echo30云南分离株KM/A363/09进行全基因组测序和分析,了解该株病毒的遗传特性。方法设计针对Echo30引物,提取病毒RNA、RT-PCR扩增和产物直接测序获得全基因组序列,利用Geneious和Mega5.1软件进行核苷酸、氨基酸序列比对及其系统进化分析,应用RDP3和SimPlot3.5.1重组软件对序列进行重组分析。结果该分离株全基因组核苷酸序列长度为7425 bp,编码2194个氨基酸。其核苷酸和氨基酸序列与其原型株Bastianni的同源性分别为81.2%和95.8%;与其他Echo30型毒株的各区段核苷酸和氨基酸同源性分别为81.2%~88.6%和95.8%~97.8%;进化分析发现KM/A363/09毒株属于中国Echo30分支中的一支。而且发现KM/A363/09株基因序列在非结构区可能存在重组事件。结论云南分离株KM/A363/09属于中国Echo30分支中的一支,而中国分离株已经发生一定的进化。
目的:對2009年從中國雲南省1名腦炎患兒糞便標本中分離到的Echo30雲南分離株KM/A363/09進行全基因組測序和分析,瞭解該株病毒的遺傳特性。方法設計針對Echo30引物,提取病毒RNA、RT-PCR擴增和產物直接測序穫得全基因組序列,利用Geneious和Mega5.1軟件進行覈苷痠、氨基痠序列比對及其繫統進化分析,應用RDP3和SimPlot3.5.1重組軟件對序列進行重組分析。結果該分離株全基因組覈苷痠序列長度為7425 bp,編碼2194箇氨基痠。其覈苷痠和氨基痠序列與其原型株Bastianni的同源性分彆為81.2%和95.8%;與其他Echo30型毒株的各區段覈苷痠和氨基痠同源性分彆為81.2%~88.6%和95.8%~97.8%;進化分析髮現KM/A363/09毒株屬于中國Echo30分支中的一支。而且髮現KM/A363/09株基因序列在非結構區可能存在重組事件。結論雲南分離株KM/A363/09屬于中國Echo30分支中的一支,而中國分離株已經髮生一定的進化。
목적:대2009년종중국운남성1명뇌염환인분편표본중분리도적Echo30운남분리주KM/A363/09진행전기인조측서화분석,료해해주병독적유전특성。방법설계침대Echo30인물,제취병독RNA、RT-PCR확증화산물직접측서획득전기인조서렬,이용Geneious화Mega5.1연건진행핵감산、안기산서렬비대급기계통진화분석,응용RDP3화SimPlot3.5.1중조연건대서렬진행중조분석。결과해분리주전기인조핵감산서렬장도위7425 bp,편마2194개안기산。기핵감산화안기산서렬여기원형주Bastianni적동원성분별위81.2%화95.8%;여기타Echo30형독주적각구단핵감산화안기산동원성분별위81.2%~88.6%화95.8%~97.8%;진화분석발현KM/A363/09독주속우중국Echo30분지중적일지。이차발현KM/A363/09주기인서렬재비결구구가능존재중조사건。결론운남분리주KM/A363/09속우중국Echo30분지중적일지,이중국분리주이경발생일정적진화。
Objective To analyze the genetic characteristics of the complete genome of a human echovirus 30 (Echo30) KM/A363/09 strain isolated in Yunnan, China in 2009.Methods Primers specif-ic for Echo30 were designed .The extracted RNA was amplified by using RT-PCR.Seven fragments covering the complete viral genome were sequenced and the complete sequences were aligned with other sequences of enterovirus reference strains downloaded from Genbank . By using Mega5.1, Geneious, RDP3 and SimPlot3.5.1 softwares, the phylogenetic and recombination analysis were carried out .Results The com-plete nucleotide sequence of KM/A363/09 isolate was 7425 bp in length, encoding 2194 amino acids.KM/A363/09 isolate was highly similar with Bastianni prototype strain showing the homology of 81.2%in nucle-otide and 95.8%in amino acid.The eight Echo30 isolates shared 81.2%-88.6%homologies in nucleotide sequences and 95.8%-97.8%in amino acid sequences .Phylogenetic analysis showed that the KM/A363/09 strain belonged to one clade of Echo 30 in China.The genetic recombination of KM/A363/09 isolate was detected in the non-structural region .Conclusion KM/A363/09 isolate belongs to one clade of Echo 30 in China indicating that the evolution of Echo 30 has occurred in China .