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
2013年
9期
688-691
,共4页
许玉玲%卫海燕%陈豪敏%黄学勇
許玉玲%衛海燕%陳豪敏%黃學勇
허옥령%위해연%진호민%황학용
手足口病%埃克病毒11型%基因特征
手足口病%埃剋病毒11型%基因特徵
수족구병%애극병독11형%기인특정
HFMD%Echovirus 11%Genetic characteristics
目的分析埃克病毒11型( Echo11)河南分离株的分子流行病学特征。方法对2010-2012年河南手足口病监测系统中采集的粪便标本,采用RD、Hep2细胞进行病毒分离,对阳性分离物进行VP1区扩增、测序,生物学软件分析测序结果,BLAST比对后确定病毒基因型;扩增10株Echo11河南分离株VP1完整编码区序列,与国内外其他Echo11病毒株进行同源性分析并构建VP1区全基因亲缘进化树,分析其进化来源及不同基因型的流行范围。结果2010-2012年河南手足口病标本共分离出184株非EV71/CA16型肠道病毒,其中Echo1110株,占5.43%。 Echo11河南株VP1区全长共876个核苷酸,编码292个氨基酸;10株Echo11河南株VP1区之间核苷酸同源性为93.1%~100%,氨基酸同源性为97.3%~100%;与原型Gregory株之间核苷酸同源性为77.8%~78.8%,氨基酸同源性为90.8%~91.8%。结论 Echo11也是引起河南省手足口病的主要病原体,河南省存在Echo11病毒A基因型的流行。
目的分析埃剋病毒11型( Echo11)河南分離株的分子流行病學特徵。方法對2010-2012年河南手足口病鑑測繫統中採集的糞便標本,採用RD、Hep2細胞進行病毒分離,對暘性分離物進行VP1區擴增、測序,生物學軟件分析測序結果,BLAST比對後確定病毒基因型;擴增10株Echo11河南分離株VP1完整編碼區序列,與國內外其他Echo11病毒株進行同源性分析併構建VP1區全基因親緣進化樹,分析其進化來源及不同基因型的流行範圍。結果2010-2012年河南手足口病標本共分離齣184株非EV71/CA16型腸道病毒,其中Echo1110株,佔5.43%。 Echo11河南株VP1區全長共876箇覈苷痠,編碼292箇氨基痠;10株Echo11河南株VP1區之間覈苷痠同源性為93.1%~100%,氨基痠同源性為97.3%~100%;與原型Gregory株之間覈苷痠同源性為77.8%~78.8%,氨基痠同源性為90.8%~91.8%。結論 Echo11也是引起河南省手足口病的主要病原體,河南省存在Echo11病毒A基因型的流行。
목적분석애극병독11형( Echo11)하남분리주적분자류행병학특정。방법대2010-2012년하남수족구병감측계통중채집적분편표본,채용RD、Hep2세포진행병독분리,대양성분리물진행VP1구확증、측서,생물학연건분석측서결과,BLAST비대후학정병독기인형;확증10주Echo11하남분리주VP1완정편마구서렬,여국내외기타Echo11병독주진행동원성분석병구건VP1구전기인친연진화수,분석기진화래원급불동기인형적류행범위。결과2010-2012년하남수족구병표본공분리출184주비EV71/CA16형장도병독,기중Echo1110주,점5.43%。 Echo11하남주VP1구전장공876개핵감산,편마292개안기산;10주Echo11하남주VP1구지간핵감산동원성위93.1%~100%,안기산동원성위97.3%~100%;여원형Gregory주지간핵감산동원성위77.8%~78.8%,안기산동원성위90.8%~91.8%。결론 Echo11야시인기하남성수족구병적주요병원체,하남성존재Echo11병독A기인형적류행。
Objective To analyze the evolution and genetic characteristics of Echovirus 11 (Echo11) strains isolated from patients with hand food and mouth disease ( HFMD) in Henan province. Methods Enterovirus strains were isolated from stool samples of patients with HFMD from year 2010 to 2012.The sequences of VP1 region of all positive strains were amplified , sequenced and then analyzed by BLSAT to determine their genotypes .The entire VP1 coding regions of 10 Echo11 strains were amplified by RT-PCR, and the homology analysis was conducted among them and other Echo 11 strains published in Gen-Bank.A phylogenetic tree was constructed to evaluate the evolution of Henan isolates and the prevalence of different genotypes .Results From year 2010 to 2012 , 184 non-Enterovirus 71 ( EV71 ) strains and non-Coxsakievirus A16 (CA16) strains causing HFMD were isolated, 10 (5.43%) of with were Echo11 strains. There were 876 nucleotides ( nt) in the complete VP1 gene sequence , encoding 292 amino acids ( aa) .The 10 Echo11 strains shared 93.1%-100% homologies in nt sequences and 97.3%-100% in aa sequences. The homology analysis indicated that Henan strains and prototype strains were highly similar but different with the homology of 77.8%-78.8% in nt and 90.8%-91.8% in aa, respectively.Conclusion Echo11 was one of the pathogens causing HFMD in He-nan province and genotype A was the dominant genotype .