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Widespread Infection with Homologues of Human Parvoviruses B19 PARV4 and Human Bocavirus of Chimpanzees and Gorillas in the Wild

机译:人类细小病毒B19PARV4和人类黑猩猩和大猩猩在野生环境中的同源病毒的同源性的广泛感染

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摘要

Infections with human parvoviruses B19 and recently discovered human bocaviruses (HBoVs) are widespread, while PARV4 infections are transmitted parenterally and prevalent specifically in injecting drug users and hemophiliacs. To investigate the exposure and circulation of parvoviruses related to B19 virus, PARV4, and HBoV in nonhuman primates, plasma samples collected from 73 Cameroonian wild-caught chimpanzees and gorillas and 91 Old World monkey (OWM) species were screened for antibodies to recombinant B19 virus, PARV4, and HBoV VP2 antigens by enzyme-linked immunosorbent assay (ELISA). Moderate to high frequencies of seroreactivity to PARV4 (63% and 18% in chimpanzees and gorillas, respectively), HBoV (73% and 36%), and B19 virus (8% and 27%) were recorded for apes, while OWMs were uniformly negative (for PARV4 and B19 virus) or infrequently reactive (3% for HBoV). For genetic characterization, plasma samples and 54 fecal samples from chimpanzees and gorillas collected from Cameroonian forest floors were screened by PCR with primers conserved within Erythrovirus, Bocavirus, and PARV4 genera. Two plasma samples (chimpanzee and baboon) were positive for PARV4, while four fecal samples were positive for HBoV-like viruses. The chimpanzee PARV4 variant showed 18% and 15% nucleotide sequence divergence in NS and VP1/2, respectively, from human variants (9% and 7% amino acid, respectively), while the baboon variant was substantially more divergent, mirroring host phylogeny. Ape HBoV variants showed complex sequence relationships with human viruses, comprising separate divergent homologues of HBoV1 and the recombinant HBoV3 species in chimpanzees and a novel recombinant species in gorillas. This study provides the first evidence for widespread circulation of parvoviruses in primates and enables future investigations of their epidemiology, host specificity, and (co)evolutionary histories.
机译:人细小病毒B19和最近发现的人博卡病毒(HBoV)感染很普遍,而PARV4感染则通过肠胃外传播,特别是在注射吸毒者和血友病患者中普遍存在。为了调查与B19病毒,PARV4和HBoV相关的细小病毒在非人类灵长类动物中的暴露和流通,从73个喀麦隆野生黑猩猩和大猩猩以及91个旧世界猴(OWM)物种收集的血浆样本中筛选了针对重组B19病毒的抗体,PARV4和HBoV VP2抗原通过酶联免疫吸附测定(ELISA)。记录到猿类对PARV4的血清反应具有中等至高频的频率(黑猩猩和大猩猩分别为63%和18%),HBoV(73%和36%)和B19病毒(8%和27%),而OWM一致阴性(对于PARV4和B19病毒)或不经常发生反应(对于HBoV为3%)。为了进行遗传学表征,通过PCR筛选了从喀麦隆森林地带收集到的黑猩猩和大猩猩的血浆样品和54份粪便样品,并使用了在红病毒,博卡病毒和PARV4属中保守的引物。两个血浆样本(黑猩猩和狒狒)对PARV4呈阳性,而四个粪便样本对HBoV样病毒呈阳性。黑猩猩的PARV4变体在NS和VP1 / 2中分别与人类变体(分别为9%和7%氨基酸)在18%和15%核苷酸序列上有差异,而狒狒变体的差异更大,反映出宿主的系统发育。猿类HBoV变体与人类病毒表现出复杂的序列关系,包括黑猩猩中HBoV1和重组HBoV3物种的分离的不同同源物,以及大猩猩中的新型重组物种。这项研究为细小病毒在灵长类动物中的广泛传播提供了第一个证据,并使未来对其流行病学,宿主特异性和(共同)进化史的研究成为可能。

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