Richins Travis, Sapp Sarah G H, Ketzis Jennifer K, Willingham Arve Lee, Mukaratirwa Samson, Qvarnstrom Yvonne, Barratt Joel L N
Centers for Disease Control and Prevention, Division of Parasitic Diseases and Malaria, Parasitic Diseases Branch, USA.
Oak Ridge Associated Universities, Oak Ridge, TN, USA.
Int J Parasitol Parasites Wildl. 2023 Feb 16;20:153-161. doi: 10.1016/j.ijppaw.2023.02.003. eCollection 2023 Apr.
Human strongyloidiasis is an important neglected tropical disease primarily caused by the nematode , and to a lesser extent which mainly infects non-human primates. Zoonotic sources of infection have important implications for control and prevention of morbidity and mortality caused by strongyloidiasis. Recent molecular evidence suggests that for primate host specificity is variable among genotypes across the Old World, and consequently that these types likely vary in their capacity for human spillover infections. Populations of free-roaming vervet monkeys (), introduced to the Caribbean Island of Staint Kitts from Africa, live in close contact with humans, and concern has arisen regarding their potential to serve as reservoirs of zoonotic infections. In this study, we sought to determine the genotypes of infecting St. Kitts vervets to explore whether they are potential reservoirs for human-infecting types. Fecal specimens were collected from St. Kitts vervets and infections were confirmed microscopically and by PCR. genotypes were determined from positive fecal specimens using an Illumina amplicon sequencing-based genotyping approach targeting the mitochondrial cox1 locus and 18S rDNA hypervariable regions I and IV of species. Phylogenetic analysis of resultant genotypes supported that from St. Kitts vervets is of an exclusively African variety, falling within the same monophyletic group as an isolate which has been detected previously in a naturally infected human from Guinea-Bissau. This observation highlights that St. Kitts vervets may serve as potential reservoirs for zoonotic infection, which warrants further exploration.
人类类圆线虫病是一种重要的被忽视的热带病,主要由线虫引起,在较小程度上也由主要感染非人类灵长类动物的线虫引起。人畜共患感染源对于控制和预防类圆线虫病所致发病和死亡具有重要意义。最近的分子证据表明,在旧大陆,不同基因型的灵长类宿主特异性存在差异,因此这些类型在人类溢出感染能力方面可能也有所不同。从非洲引入加勒比海圣基茨岛的自由放养的黑长尾猴种群与人类密切接触,人们担心它们可能成为人畜共患感染的储存宿主。在本研究中,我们试图确定感染圣基茨黑长尾猴的类圆线虫基因型,以探讨它们是否是人类感染性类圆线虫类型的潜在储存宿主。从圣基茨黑长尾猴采集粪便标本,通过显微镜检查和PCR确认类圆线虫感染。使用基于Illumina扩增子测序的基因分型方法,针对线粒体细胞色素氧化酶亚基1(cox1)基因座以及类圆线虫物种的18S核糖体DNA(rDNA)高变区I和IV,从阳性粪便标本中确定类圆线虫基因型。对所得基因型进行系统发育分析支持,圣基茨黑长尾猴体内的类圆线虫属于纯非洲变种,与先前在几内亚比绍一名自然感染人类中检测到的分离株属于同一单系群。这一观察结果突出表明,圣基茨黑长尾猴可能是类圆线虫人畜共患感染的潜在储存宿主,这值得进一步探索。