中华流行病学杂志
中華流行病學雜誌
중화류행병학잡지
CHINESE JOURNAL OF EPIDEMIOLOGY
2009年
11期
1179-1183
,共5页
董慧瑾%钱渊%张又%赵林清%朱汝南%陈冬梅%刘立颖
董慧瑾%錢淵%張又%趙林清%硃汝南%陳鼕梅%劉立穎
동혜근%전연%장우%조림청%주여남%진동매%류립영
G9型轮状病毒%基因型%序列分析
G9型輪狀病毒%基因型%序列分析
G9형륜상병독%기인형%서렬분석
Rotaviras G9%Genotype%Sequence analysis
目的 了解北京地区2007-2008年检测到的G9型A组人轮状病毒外壳蛋白VP7和VP4的基因特征.方法 选取经过轮状病毒核酸杂交方法检测为G9型轮状病毒的12份儿童腹泻患儿的粪便标本,应用针对VP7全长基因的特异引物对进行RT-PCR扩增,对所获得的VP7全长基因进行克隆和测序,将所获得的序列与GenBank中的G9型原型病毒株和近期流行株的VP7基因进行序列和种系进化分析;经巢式PCR对G9型的VP4进行P基因分型.结果 12株G9型轮状病毒经VP7基因的序列比较分析得到确认.P基因分型结果显示北京地区近年来存在G9P[8]和G9P[6]型两种组合的轮状病毒感染.序列和种系进化分析发现北京G9型株VP7基因与世界范围内近期流行的G9型株一样都属于进化分支Ⅲ,彼此间的核苷酸和氨基酸同源性较高,而与国内最早报道的G9型T203进化关系较远,且北京G9P[8]和G9P[6]型株分别与国内近期报道的新疆G9P[8]和G9P[6]型株及相应的武汉G9型株VP7基因,在氨基酸位点上存在一些共同的氨基酸残基取代.结论 北京地区近年存在G9P[8]和G9P[6]两种不同基因组合的G9型轮状病毒感染,需要进一步加强对G9型轮状病毒的分子流行病学监测.
目的 瞭解北京地區2007-2008年檢測到的G9型A組人輪狀病毒外殼蛋白VP7和VP4的基因特徵.方法 選取經過輪狀病毒覈痠雜交方法檢測為G9型輪狀病毒的12份兒童腹瀉患兒的糞便標本,應用針對VP7全長基因的特異引物對進行RT-PCR擴增,對所穫得的VP7全長基因進行剋隆和測序,將所穫得的序列與GenBank中的G9型原型病毒株和近期流行株的VP7基因進行序列和種繫進化分析;經巢式PCR對G9型的VP4進行P基因分型.結果 12株G9型輪狀病毒經VP7基因的序列比較分析得到確認.P基因分型結果顯示北京地區近年來存在G9P[8]和G9P[6]型兩種組閤的輪狀病毒感染.序列和種繫進化分析髮現北京G9型株VP7基因與世界範圍內近期流行的G9型株一樣都屬于進化分支Ⅲ,彼此間的覈苷痠和氨基痠同源性較高,而與國內最早報道的G9型T203進化關繫較遠,且北京G9P[8]和G9P[6]型株分彆與國內近期報道的新疆G9P[8]和G9P[6]型株及相應的武漢G9型株VP7基因,在氨基痠位點上存在一些共同的氨基痠殘基取代.結論 北京地區近年存在G9P[8]和G9P[6]兩種不同基因組閤的G9型輪狀病毒感染,需要進一步加彊對G9型輪狀病毒的分子流行病學鑑測.
목적 료해북경지구2007-2008년검측도적G9형A조인륜상병독외각단백VP7화VP4적기인특정.방법 선취경과륜상병독핵산잡교방법검측위G9형륜상병독적12빈인동복사환인적분편표본,응용침대VP7전장기인적특이인물대진행RT-PCR확증,대소획득적VP7전장기인진행극륭화측서,장소획득적서렬여GenBank중적G9형원형병독주화근기류행주적VP7기인진행서렬화충계진화분석;경소식PCR대G9형적VP4진행P기인분형.결과 12주G9형륜상병독경VP7기인적서렬비교분석득도학인.P기인분형결과현시북경지구근년래존재G9P[8]화G9P[6]형량충조합적륜상병독감염.서렬화충계진화분석발현북경G9형주VP7기인여세계범위내근기류행적G9형주일양도속우진화분지Ⅲ,피차간적핵감산화안기산동원성교고,이여국내최조보도적G9형T203진화관계교원,차북경G9P[8]화G9P[6]형주분별여국내근기보도적신강G9P[8]화G9P[6]형주급상응적무한G9형주VP7기인,재안기산위점상존재일사공동적안기산잔기취대.결론 북경지구근년존재G9P[8]화G9P[6]량충불동기인조합적G9형륜상병독감염,수요진일보가강대G9형륜상병독적분자류행병학감측.
Objective To characterize the outer capsid protein VP7 and VP4 encoding genes of human rotavirus G9 strains detected in Beijing, from 2007 to 2008. Methods Full length of VP7 genes of G9 rotaviruses from 12 fecal specimens previously detected by dot-blot hybridization assay were amplified by RT-PCR and sequenced after being cloned into T vector. The sequences of these VP7s were compared to VP7 genes of rotaviras G9 prototype strains and recently circulating strains around the world. VP4 genes of these 12 G9 strains were amplified by nested-PCR for P genotyping. Results Sequence analysis for the full length of VP7 genes from these 12 specimens confirmed that they were G9 rotaviruses. P genotyping for VP4 genes revealed that both P[8]G9 and P [6] G9 were circulating in Beijing in the last 2 years. Sequence and phylogenetic analysis demonstrated that VP7 genes of G9 strains from Beijing in this study were clustered in the lineage Ⅲ which resembled the G9 strains circulating in other places around the world, indicated by high identities of nucleotide and deduced amino acid sequences and were distant with the first reported G9 strain T203 identified in China in 1994. It was found that there were some consistent amino acid substitutes at the corresponding positions among VP7s from these 12 specimens and from Xinjiang and Wuhan, both in G9P [8] and G9P [6] strains. Conclusion The rotavirus G9 strains both in combination of G9P [8]and G9P [6] were circulating in Beijing in the past years. It seemed that rotavirus G9 should be included in the list of surveillance for rotavirus in China.