Gao Li-dong, Cai Liang, Liu Fu-qiang, Zhang Hong, Hu Shi-xiong, Tao Xiao-yan, Li Hao, Liu Jia-hui, Wang Shi-qing, Tang Qing, Liu Yun-zhi
Hunan Provincial Center for Disease Control and Prevention, Changsha, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2011 Oct;32(10):1001-4.
To analyze the etiology of rabies in Hunan province and the genetic characteristics of rabies N gene isolated from 2008 to 2009.
Direct immunofluorescence assay (DFA) and nested PCR were employed to detect the monitoring samples including brain tissues of dogs and saliva, serum or urine which were collected in 2008 to 2009, from the rabies patients. Positive samples were sequenced by ABI3730 gene analyzer for the full length of the N gene target. The homology and hpylogeography of the rabies virus were analyzed after the phylogenetic tree was constructed by Blast, Clustal W and Mega 4.0 software.
Of the 1451 tissue samples from the dogs' brain, 31 were positive under DFA and the positive rate was 2.14%. The DFA positive samples were redetected by RT-PCR and the positive rate was 1.17%. 56 samples of saliva, serum and urine samples were detected by RT-PCR from the rabies patients, with 3 positives and the positive rate was 5.36%. The length of nest PCR products were 255 bp. The rates of homology to the nucleotide and the amino acid of rabies N gene were 87.2% - 87.9% after compared to the pasture strain. The phylogenetic tree was successfully built and 20 strains isolated lately belonged to the rabies gene type I.
The epidemic situation of human and dogs rabies in Human were relatively stable, with all the isolated rabies virus belonging to genotype I, without any variation.
分析湖南省狂犬病的病原学特征及2008 - 2009年分离的狂犬病N基因的遗传特性。
采用直接免疫荧光法(DFA)和巢式PCR对2008 - 2009年采集的狂犬病患者的犬脑组织、唾液、血清或尿液等监测样本进行检测。对阳性样本用ABI3730基因分析仪进行N基因全长测序。利用Blast、Clustal W和Mega 4.0软件构建系统发育树,分析狂犬病病毒的同源性和遗传地理学特征。
1451份犬脑组织样本中,DFA检测阳性31份,阳性率为2.14%。对DFA阳性样本进行RT-PCR复检,阳性率为1.17%。对狂犬病患者的56份唾液、血清和尿液样本进行RT-PCR检测,阳性3份,阳性率为5.36%。巢式PCR产物长度为255 bp。与巴斯德株比较,狂犬病N基因核苷酸和氨基酸同源率为87.2% - 87.9%。成功构建系统发育树,近期分离的20株均属于狂犬病基因I型。
湖南省人和犬狂犬病疫情相对稳定,分离的狂犬病病毒均属于I型,未出现变异。