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Isolation and identification of a variant subtype G 2b porcine epidemic diarrhea virus and S gene sequence characteristic

机译:变体亚型G 2B猪流行病腹泻病毒和S基因序列特征的分离与鉴定

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Porcine epidemic diarrhea (PED) which is caused by porcine epidemic diarrhea virus (PEDV), is an intestinal communicable disease. In recent years, though pigs have been immunized with the vaccines in pig farms, PED still broke out and caused severe economic losses to the swine industry in the northeast China. In this study, the sample was positive for PEDV variant strains via the nano-nest PCR. The strain was successfully isolated from positive samples and was serially passaged in Vero-E6 cells. In addition, the strain was identified via electron microscopy observation, indirect immunofluorescence assay and infection experiment in newborn piglets and named PEDV CH/JLDH/2016 strain (Accession No. MF346935). Phylogenetic analysis of the S gene showed that the CH/JLDH/2016 strain was clustered into G2b subgroup. Comparing with the CV777 vaccine strain, amino acid sequence analysis of CH/JLDH/2016 strain showed that 15 nucleotides were inserted and 9 were absent in S gene, whose amino acid sequence it educed insertions of 5 amino acids((58)NQGX(61) and N-145) and absences of 3 amino acids((RD165)-R-164 and Y-1204). Our strain, in the SS2 epitope have no amino acid, variant while in SS6 epitope, Y changed into S in 776th amino acid. The results indicated that PEDV G2b variant strains have been emerged in Jilin province. The identification of new types of PEDV variant strains would stimulate the development of effective vaccines for the prevention and control of PED. The novel vaccines that based on these newly identified PEDV variant strains may contribute to the control of PED outbreaks in China.
机译:猪疫情腹泻(PED)由猪流行性腹泻病毒(PEDV)引起的,是一种肠道传染病。近年来,虽然猪在猪场的疫苗免疫疫苗,但PED仍爆发并导致了中国东北地区猪业的严重经济损失。在该研究中,样品通过纳米巢PCR为PEDV变异菌株阳性。从阳性样品中成功分离菌株,并在Vero-E6细胞中连续传代。此外,通过电子显微镜观察,间接免疫荧光测定和新生仔猪的感染试验鉴定该菌株,并命名为PEDV CH / JLDH / 2016菌株(登录号MF346935)。 S基因的系统发育分析表明,CH / JLDH / 2016菌株聚集成G2B亚组。与CV777疫苗菌株进行比较,CH / JLDH / 2016菌株的氨基酸序列分析显示插入15个核苷酸,在S基因中不存在9个,其氨基酸序列被引导地插入5个氨基酸((58)NQGX(61 )和N-145)和3个氨基酸((RD165)-R-164和Y-1204)。我们的菌株,在SS2表位没有氨基酸,变体在SS6表位时,Y在776氨基酸中改变为S。结果表明,吉林省出现了PEDV G2B变异菌株。新型PEDV变异菌株的鉴定将刺激预防和控制PED的有效疫苗的发展。基于这些新发现的PEDV变异菌株的新型疫苗可能有助于控制中国的PED爆发。

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