Jiang Yong-zhen, Lu Jian, Zhang Li-ping, Tian Rui-guang, Liu Qing-lian, Bi Sheng-li
National Institute for Viral Disease Control and Prevention, China CDC, Beijing 100052, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2008 Dec;22(6):468-71.
To investigate the seroprevalence of HEV infection and genotype.
ELISA were used for detecting anti-HEV IgG of the serum samples, the nested reverse transcriptase PCR (RT-nPCR) was used for detecting HEV RNA in patient serum and swine bile samples. All samples were collected in 2005-2007 in some districts in Sichuan province. The primers used for genotyping were the ORF2 region of HEV genome.
The anti-HEV IgG was detected positive in childrens 6.10% (41/672), adults 42.26% (280/ 661), swines 88.89% (32/36), chickens negative (0/59). 1 case of 15 serum samples of anti-HEV IgM positive and 3 of 54 swine bile samples were positive for HEV RNA by RT-PCR.Sequence analysis of 4 isolates has 92.1% to 98.6% nucleotide sequence homology. These isolates from human and swine were identified closely related to Ch-T21 strain 90.1%-96.9% sequence homology, which belonged to HEV genotype 4B.
The swine were the risk factors in the spread of hepatitis E virus.
调查戊型肝炎病毒(HEV)感染的血清流行率及基因型。
采用酶联免疫吸附测定(ELISA)检测血清样本中的抗HEV IgG,采用巢式逆转录聚合酶链反应(RT - nPCR)检测患者血清和猪胆汁样本中的HEV RNA。所有样本于2005 - 2007年在四川省部分地区采集。用于基因分型的引物为HEV基因组的开放阅读框2(ORF2)区域。
抗HEV IgG检测儿童阳性率为6.10%(41/672),成人阳性率为42.26%(280/661),猪阳性率为88.89%(32/36),鸡为阴性(0/59)。15份抗HEV IgM阳性血清样本中有1份、54份猪胆汁样本中有3份经RT - PCR检测HEV RNA呈阳性。4株分离株的序列分析显示核苷酸序列同源性为92.1%至98.6%。这些来自人和猪的分离株与Ch - T21株的序列同源性为90.1% - 96.9%,属于HEV基因型4B。
猪是戊型肝炎病毒传播的危险因素。