Department of Biotechnology, Quaid-i-Azam University, Islamabad, Pakistan.
PLoS One. 2013 Nov 12;8(11):e78377. doi: 10.1371/journal.pone.0078377. eCollection 2013.
Human parechoviruses are known to cause asymptomatic to severe clinical illness predominantly respiratory and gastroenetric infections. Despite their global prevalence, epidemiological studies have not been performed in Pakistan. In this study, we retrospectively analyzed 110 fecal specimen and found 26 (24%) positive for viral RNA with HPeV-10 (n = 3, 23%), HPeV-13 (n = 4, 31%) and HPeV-15 (n = 6, 46%) genotypes. Clinical features of patients with different HPeV genotypes were compared. All HPeV positive children were aged ≤4 years (mean 13.92 months). The male-to-female ratio was 1: 1.17 (46.2 vs 53.8%) with significant association (p = .031) to HPeV infectivity. HPeV-10 and -13 were found during summer while HPeV-15 was only detected during late winter season. Disease symptoms were more severe in children infected with HPeV-10 and -13 as compared to HPeV-15. Fever and vomiting were observed in 100% cases of HPeV-10 and -13 while only 17% patients of HPeV-15 had these complaints. Phylogenetic analyses showed that HPeV-10, -13 and -15 strains found in this study have 9-13%, 16.8% and 21.8% nucleotide divergence respectively from the prototype strains and were clustered to distinct genetic lineages. This is the first report of HPeV-15 infection in humans although first identified in rhesus macaques. The arginine-glycine-aspartic acid (RGD) motif present at the C-terminal of VP1 responsible for the viral attachment to cellular integrins was not found in all of these strains. In conclusion, these findings enhance our knowledge related to the epidemiology and genetic diversity of the HPeV in Pakistan and support the need for continued laboratory based surveillance programs especially in infants and neonatal clinical settings. Further, the parechovirus pathogenesis, cross-species transmission and disease reservoirs must be ascertained to adopt better prevention measures.
人肠道病毒已知可引起无症状至严重临床疾病,主要为呼吸道和胃肠道感染。尽管它们在全球范围内普遍存在,但在巴基斯坦尚未进行过流行病学研究。在这项研究中,我们回顾性分析了 110 份粪便标本,发现 26 份(24%)病毒 RNA 呈阳性,其中 HPeV-10(n=3,23%)、HPeV-13(n=4,31%)和 HPeV-15(n=6,46%)基因型。比较了不同 HPeV 基因型患者的临床特征。所有 HPeV 阳性患儿年龄均≤4 岁(平均 13.92 个月)。男女性别比为 1:1.17(46.2 对 53.8%),与 HPeV 感染有显著相关性(p=0.031)。HPeV-10 和 -13 是在夏季发现的,而 HPeV-15 仅在冬末季节检测到。与 HPeV-15 相比,感染 HPeV-10 和 -13 的患儿症状更严重。100%的 HPeV-10 和 -13 患儿出现发热和呕吐,而只有 17%的 HPeV-15 患儿有这些症状。系统进化分析显示,本研究中发现的 HPeV-10、-13 和 -15 株与原型株的核苷酸差异分别为 9-13%、16.8%和 21.8%,并聚类为不同的遗传谱系。这是 HPeV-15 在人类中的首次感染报告,尽管它首先在恒河猴中被发现。位于 VP1 末端负责病毒与细胞整合素结合的精氨酸-甘氨酸-天冬氨酸(RGD)基序在所有这些毒株中均未发现。总之,这些发现增加了我们对 HPeV 在巴基斯坦的流行病学和遗传多样性的了解,并支持需要继续进行基于实验室的监测计划,特别是在婴儿和新生儿临床环境中。此外,必须确定 parechovirus 的发病机制、跨物种传播和疾病储库,以采取更好的预防措施。