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Epidemics and Frequent Recombination within Species in Outbreaks of Human Enterovirus B-Associated Hand Foot and Mouth Disease in Shandong China in 2010 and 2011

机译:2010年和2011年中国山东省与人类肠道病毒B相关的手足口病暴发的种内流行病和频繁重组

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摘要

The epidemiology and molecular characteristics of human enterovirus B (HEV-B) associated with hand, foot and mouth disease (HFMD) outbreaks in China are not well known. In the present study, we tested 201 HEV isolates from 233 clinical specimens from patients with severe HFMD during 2010–2011 in Linyi, Shandong, China. Of the 201 isolates, 189 were fully typed and 18 corresponded to HEV-B species (six serotypes CVA9, CVB1, CVB4, Echo 6, Echo 25 and Echo 30) using sensitive semi-nested polymerase chain reaction analysis of VP1 gene sequences. Phylogenetic analysis based on the VP1 region showed that eight E30SD belonged to a novel sub-genogroup D2; E25SD belonged to a novel sub-genogroup D6; E6SD belonged to sub-lineage C6 and five CVB1SD belonged to subgroup 4C; and B4SD belonged sub-lineage D2. The full viral genomes of the CVB1SD, E6SD, E25SD and E30SD isolates were sequenced. Analysis of phylogenetic and similarity plots indicated that E25SD recombined with E25-HN-2, E30FDJS03 and E4AUS250 at noncontiguous P2A–P3D regions, while E30SD, E30FDJ03, E25-HN-2 and E9 DM had shared sequences in discrete regions of P2 and P3. Both E6SD and B1SD shared sequences with E1-HN, B4/GX/10, B5-HN, and A9-Alberta in contiguous regions of most of P2 and P3. Genetic algorithm recombination detection analysis further confirmed the existence of multiple potential recombination points. In conclusion, analysis of the complete genomes of E25SD, E30SD, CVB1SD and E6SD isolated from HFMD patients revealed that they formed novel subgenogroup. Given the prevalence and recombination of these viruses in outbreaks of HFMD, persistent surveillance of HFMD-associated HEV-B pathogens is required to predict potential emerging viruses and related disease outbreaks.
机译:在中国,与人类手足口病(HFMD)爆发有关的人类肠道病毒B(HEV-B)的流行病学和分子特征尚不清楚。在本研究中,我们在2010-2011年间在中国山东临沂对233例重度手足口病患者的临床标本进行了201株HEV分离株的检测。使用VP1基因序列的敏感半巢式聚合酶链反应分析,在201个分离株中,有189个完全分型,其中18个对应于HEV-B物种(六个血清型CVA9,CVB1,CVB4,Echo 6,Echo 25和Echo 30)。基于VP1区域的系统发育分析表明,八个E30SD属于一个新的亚基因组D2; E25SD属于一个新的亚基因组D6。 E6SD属于子系C6,五个CVB1SD属于子组4C; B4SD和B4SD属于子血统D2。对CVB1SD,E6SD,E25SD和E30SD分离株的完整病毒基因组进行了测序。系统发育和相似性图分析表明,E25SD与E25-HN-2,E30FDJS03和E4AUS250在不连续的P2A-P3D区域重组,而E30SD,E30FDJ03,E25-HN-2和E9 DM在P2和P3的离散区域具有共享序列。 E6SD和B1SD都在大多数P2和P3的连续区域中与E1-HN,B4 / GX / 10,B5-HN和A9-Alberta共享序列。遗传算法重组检测分析进一步证实了多个潜在重组点的存在。总之,对分离自手足口病患者的E25SD,E30SD,CVB1SD和E6SD完整基因组的分析表明,它们形成了新的亚基因组。考虑到这些病毒在HFMD爆发中的流行和重组,需要持续监测与HFMD相关的HEV-B病原体,以预测潜在的新兴病毒和相关疾病的爆发。

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