Parasitology Reference and Research Laboratory, National Centre of Microbiology, Carretera de Majadahonda a Pozuelo Km 2 Majadahonda, 28220, Madrid, Spain.
Department of Animal Ecology and Tropical Biology, Biocenter, Universität Würzburg, Am Hubland, Würzburg, Germany.
Primates. 2022 Jan;63(1):41-49. doi: 10.1007/s10329-021-00963-1. Epub 2022 Jan 8.
The western chimpanzee (Pan troglodytes verus), a subspecies of the common chimpanzee, is currently listed as Critically Endangered. Human-driven habitat loss and infectious diseases are causing dramatic chimpanzee population declines and range contractions that are bringing these primates to the brink of extinction. Little information is currently available on the occurrence of diarrhoea-causing enteric protist species in chimpanzees in general, and in western chimpanzees in particular, or on the role of humans as a potential source of these infections. In this prospective molecular epidemiological study, we investigated the presence, genetic variability, and zoonotic potential of enteric protists in faecal samples from western chimpanzees (n = 124) and humans (n = 9) in Comoé National Park, Côte d'Ivoire. Parasite detection and genotyping were conducted by using polymerase chain reaction (PCR) and Sanger sequencing. The protist species found in the chimpanzee samples were Entamoeba dispar (14.5%), Blastocystis sp. (11.3%), Giardia duodenalis (5.8%), Troglodytella abrassarti (2.5%) and Cryptosporidium hominis (0.8%). The protist species found in the human samples were G. duodenalis (22.2%) and Blastocystis sp. (11.1%). Entamoeba histolytica, Enterocytozoon bieneusi, and Balantioides coli were undetected in both chimpanzee and human samples. Sequence analyses revealed the presence of Blastocystis subtype (ST) 1 (alleles 4 and 8) and ST3 (allele 24) in chimpanzees, and ST3 (allele 52) in humans. ST1 allele 8 represents a chimpanzee-adapted Blastocystis genetic variant. Cross-species transmission of pathogenic enteric protists between chimpanzees and humans might be possible in Comoé National Park, although the frequency and extent of zoonotic events remain to be fully elucidated.
西部黑猩猩(Pan troglodytes verus),普通黑猩猩的一个亚种,目前被列为极危物种。人类驱动的栖息地丧失和传染病导致黑猩猩数量急剧下降和栖息地收缩,使这些灵长类动物濒临灭绝。目前关于普通黑猩猩,特别是西部黑猩猩中引起腹泻的肠原生动物物种的发生情况,以及人类作为这些感染的潜在来源的作用,信息很少。在这项前瞻性分子流行病学研究中,我们调查了科莫埃国家公园(科特迪瓦)西部黑猩猩(n=124)和人类(n=9)粪便样本中肠原生动物的存在、遗传变异性和人畜共患潜力。寄生虫检测和基因分型采用聚合酶链反应(PCR)和 Sanger 测序进行。在黑猩猩样本中发现的原生动物物种为迪斯帕氏内阿米巴(14.5%)、芽囊原虫(11.3%)、十二指肠贾第鞭毛虫(5.8%)、阿布拉萨提氏滴虫(2.5%)和人隐孢子虫(0.8%)。在人类样本中发现的原生动物物种为十二指肠贾第鞭毛虫(22.2%)和芽囊原虫(11.1%)。溶组织内阿米巴、肠内细胞球虫和结肠小袋纤毛虫在黑猩猩和人类样本中均未检测到。序列分析显示,在黑猩猩中存在芽囊原虫亚型(ST)1(等位基因 4 和 8)和 ST3(等位基因 24),在人类中存在 ST3(等位基因 52)。ST1 等位基因 8 代表一种适应黑猩猩的芽囊原虫遗传变异。在科莫埃国家公园,黑猩猩和人类之间可能存在致病性肠原生动物的种间传播,尽管人畜共患病事件的频率和程度仍有待充分阐明。