Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Ngamba Island Chimpanzee Sanctuary/Chimpanzee Trust, Entebbe, Uganda.
Am J Primatol. 2023 Jan;85(1):e23452. doi: 10.1002/ajp.23452. Epub 2022 Nov 3.
Infectious disease is a major concern for both wild and captive primate populations. Primate sanctuaries in Africa provide critical protection to thousands of wild-born, orphan primates confiscated from the bushmeat and pet trades. However, uncertainty about the infectious agents these individuals potentially harbor has important implications for their individual care and long-term conservation strategies. We used metagenomic next-generation sequencing to identify viruses in blood samples from chimpanzees (Pan troglodytes) in three sanctuaries in West, Central, and East Africa. Our goal was to evaluate whether viruses of human origin or other "atypical" or unknown viruses might infect these chimpanzees. We identified viruses from eight families: Anelloviridae, Flaviviridae, Genomoviridae, Hepadnaviridae, Parvoviridae, Picobirnaviridae, Picornaviridae, and Rhabdoviridae. The majority (15/26) of viruses identified were members of the family Anelloviridae and represent the genera Alphatorquevirus (torque teno viruses) and Betatorquevirus (torque teno mini viruses), which are common in chimpanzees and apathogenic. Of the remaining 11 viruses, 9 were typical constituents of the chimpanzee virome that have been identified in previous studies and are also thought to be apathogenic. One virus, a novel tibrovirus (Rhabdoviridae: Tibrovirus) is related to Bas-Congo virus, which was originally thought to be a human pathogen but is currently thought to be apathogenic, incidental, and vector-borne. The only virus associated with disease was rhinovirus C (Picornaviridae: Enterovirus) infecting one chimpanzee subsequent to an outbreak of respiratory illness at that sanctuary. Our results suggest that the blood-borne virome of African sanctuary chimpanzees does not differ appreciably from that of their wild counterparts, and that persistent infection with exogenous viruses may be less common than often assumed.
传染病是野生和圈养灵长类动物种群的主要关注点。非洲的灵长类动物保护区为数以千计的从丛林肉和宠物贸易中没收的野生出生、孤儿灵长类动物提供了重要保护。然而,这些个体潜在携带的传染病原体的不确定性对他们的个体护理和长期保护策略有重要影响。我们使用宏基因组下一代测序技术来鉴定来自三个位于西非、中非和东非的保护区的黑猩猩(Pan troglodytes)的血液样本中的病毒。我们的目标是评估这些黑猩猩是否可能感染人类来源的病毒或其他“非典型”或未知病毒。我们从八个科中鉴定出了病毒:细小病毒科、黄病毒科、基因组病毒科、嗜肝病毒科、细小病毒科、双顺反子病毒科、小核糖核酸病毒科和弹状病毒科。鉴定出的病毒中大多数(15/26)属于细小病毒科,属于 Alphatorquevirus(torque teno 病毒)和 Betatorquevirus(torque teno mini 病毒)属,这些病毒在黑猩猩中很常见且无致病性。在其余的 11 种病毒中,有 9 种是以前研究中已确定的黑猩猩病毒组的典型成员,也被认为是无致病性的。有一种病毒是一种新的 Tibrovirus(弹状病毒科:Tibrovirus),与最初被认为是人类病原体的 Bas-Congo 病毒有关,但现在被认为是无致病性的、偶然的和媒介传播的。唯一与疾病相关的病毒是感染了一只黑猩猩的鼻病毒 C(小核糖核酸病毒科:肠道病毒),该病毒是在该保护区发生呼吸道疾病爆发后感染的。我们的结果表明,非洲保护区黑猩猩的血液传播病毒组与野生黑猩猩的病毒组没有明显差异,并且外源性病毒的持续感染可能比通常认为的要少见。