中华实验和临床病毒学杂志
中華實驗和臨床病毒學雜誌
중화실험화림상병독학잡지
CHINESE JOURNAL OF EXPERIMENTAL AND CLINICAL VIROLOGY
2012年
5期
352-355
,共4页
艾军红%谢正德%刘春艳%高立伟%闫静
艾軍紅%謝正德%劉春豔%高立偉%閆靜
애군홍%사정덕%류춘염%고립위%염정
爱波斯坦巴尔病毒感染%爱波斯坦巴尔病毒核抗原%膜蛋白质类%儿童,住院
愛波斯坦巴爾病毒感染%愛波斯坦巴爾病毒覈抗原%膜蛋白質類%兒童,住院
애파사탄파이병독감염%애파사탄파이병독핵항원%막단백질류%인동,주원
Epstein-Barr virus infections%Epstein-Barr virus nuclear antigens%Membrane proteins%Child,hospitalized
目的 分析2005-2010年北京地区儿童原发性EBV感染流行株EBNA1与LMP1基因特征,为研究EBV变异株与疾病临床表型间是否存在相关性提供背景资料.方法 应用PCR方法扩增EBV的EBNA3C、EBNA1和LMP1基因片段,测序后应用BioEdit 7.0.9和Mega 4.0.2软件进行序列分析.结果 62例进行了EBV分型,以EBV-Ⅰ型为主,检出率为98%.62例EBNA1基因扩增阳性,其中V-val亚型(均是Vvv1变异株)为98%.50例LMP1基因羧基段扩增阳性,以China 1为主,其检出率为90%.Vvv1变异株和China 1变异株在EBV-IM与EBV-HLH中的检出率差异均无统计学意义(P=1.00).40例进行了多基因连锁分析,其中EBV-Ⅰ型、EBNA1-Vvv1变异株和LMP1-China 1变异株高度连锁,其连锁检出率为90%.35例患儿LMP1基因全长扩增阳性,CG1-CG4的检出率分别为85%、6%、6%和3%.结论 北京地区儿童原发性EBV感染疾病中,EBV亚型以EBV-Ⅰ型为主,Vvv1变异株和China 1变异株分别是EBNA1和LMP1变异株中的优势变异株,且二者高度连锁.儿童原发性EBV感染流行株可以分为CG1-4组,其中以CG1为主.
目的 分析2005-2010年北京地區兒童原髮性EBV感染流行株EBNA1與LMP1基因特徵,為研究EBV變異株與疾病臨床錶型間是否存在相關性提供揹景資料.方法 應用PCR方法擴增EBV的EBNA3C、EBNA1和LMP1基因片段,測序後應用BioEdit 7.0.9和Mega 4.0.2軟件進行序列分析.結果 62例進行瞭EBV分型,以EBV-Ⅰ型為主,檢齣率為98%.62例EBNA1基因擴增暘性,其中V-val亞型(均是Vvv1變異株)為98%.50例LMP1基因羧基段擴增暘性,以China 1為主,其檢齣率為90%.Vvv1變異株和China 1變異株在EBV-IM與EBV-HLH中的檢齣率差異均無統計學意義(P=1.00).40例進行瞭多基因連鎖分析,其中EBV-Ⅰ型、EBNA1-Vvv1變異株和LMP1-China 1變異株高度連鎖,其連鎖檢齣率為90%.35例患兒LMP1基因全長擴增暘性,CG1-CG4的檢齣率分彆為85%、6%、6%和3%.結論 北京地區兒童原髮性EBV感染疾病中,EBV亞型以EBV-Ⅰ型為主,Vvv1變異株和China 1變異株分彆是EBNA1和LMP1變異株中的優勢變異株,且二者高度連鎖.兒童原髮性EBV感染流行株可以分為CG1-4組,其中以CG1為主.
목적 분석2005-2010년북경지구인동원발성EBV감염류행주EBNA1여LMP1기인특정,위연구EBV변이주여질병림상표형간시부존재상관성제공배경자료.방법 응용PCR방법확증EBV적EBNA3C、EBNA1화LMP1기인편단,측서후응용BioEdit 7.0.9화Mega 4.0.2연건진행서렬분석.결과 62례진행료EBV분형,이EBV-Ⅰ형위주,검출솔위98%.62례EBNA1기인확증양성,기중V-val아형(균시Vvv1변이주)위98%.50례LMP1기인최기단확증양성,이China 1위주,기검출솔위90%.Vvv1변이주화China 1변이주재EBV-IM여EBV-HLH중적검출솔차이균무통계학의의(P=1.00).40례진행료다기인련쇄분석,기중EBV-Ⅰ형、EBNA1-Vvv1변이주화LMP1-China 1변이주고도련쇄,기련쇄검출솔위90%.35례환인LMP1기인전장확증양성,CG1-CG4적검출솔분별위85%、6%、6%화3%.결론 북경지구인동원발성EBV감염질병중,EBV아형이EBV-Ⅰ형위주,Vvv1변이주화China 1변이주분별시EBNA1화LMP1변이주중적우세변이주,차이자고도련쇄.인동원발성EBV감염류행주가이분위CG1-4조,기중이CG1위주.
Objective To analyze the characteristic of nuclear antigen 1 gene and latent membrane protein 1 gene of Epstein-Barr virus in primary EBV infection in children in Beijing area in 2005-2012.Methods Polymerase chain reaction (PCR) was used to amplify the EBNA-3C,EBNA1 and LMP1 genes.The amplified products were sequenced directly and the sequences were analyzed by BioEdit 7.0.9 and MEGA 4.0.2.Results Type A EBV was detected in 98% samples.Nucleotide sequence analysis of the carboxy-terminal region of EBNA1 showed that Vvv1 was deteted in 98% samples.DNA sequence analysis of LMP1 C-terminus indicated that China 1 was 90% in this study.There were no significant differences in the frequency of Vvv1 and China 1 between the IM and HLH samples (P =1.00).Linkage analysis of EBV types,EBNA1 and LMP1 variants indicated that 90% of EBV type A was associated with EBNA1-Vvv1 variant and LMP1-China 1 variant in 40 cases.Full length of LMP1 gene was successfully amplified in 35 cases.Four Chinese groups (CG1-4) were identified.The percentage of CG1-CG4 were 85%,6%,6% and 3%,respectively.Conclusion EBV type A is predominant in primary EBV infection in children in Beijing Area.EBNA1-Vvv1 and LMP1-China 1 variants were predominant genotypes in this area.There is a high linkage between EBNA1-Vvv1 variant and LMP1-China 1 variant.Four Chinese groups (CG1-4) were identified according to the full length of LMP1 gene and CG1 was the most prevalent.