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首页> 外文期刊>International Journal for Parasitology: Parasites and Wildlife >Are molecular tools clarifying or confusing our understanding of the public health threat from zoonotic enteric protozoa in wildlife?
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Are molecular tools clarifying or confusing our understanding of the public health threat from zoonotic enteric protozoa in wildlife?

机译:分子工具是否澄清或混淆了我们对野生动物中人畜共患的肠道原生动物的公共健康威胁的理解?

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Emerging infectious diseases are frequently zoonotic, often originating in wildlife, but enteric protozoa are considered relatively minor contributors. Opinions regarding whether pathogenic enteric protozoa may be transmitted between wildlife and humans have been shaped by our investigation tools, and have led to oscillations regarding whether particular species are zoonotic or have host-adapted life cycles. When the only approach for identifying enteric protozoa was morphology, it was assumed that many enteric protozoa colonized multiple hosts and were probably zoonotic. When molecular tools revealed genetic differences in morphologically identical species colonizing humans and other animals, host specificity seemed more likely. Parasites from animals found to be genetically identical - at the few genes investigated - to morphologically indistinguishable parasites from human hosts, were described as having zoonotic potential. More discriminatory molecular tools have now sub-divided some protozoa again. Meanwhile, some infection events indicate that, circumstances permitting, some “host-specific” protozoa, can actually infect various hosts. These repeated changes in our understanding are linked intrinsically to the investigative tools available. Here we review how molecular tools have assisted, or sometimes confused, our understanding of the public health threat from nine enteric protozoa and example wildlife hosts ( Balantoides coli - wild boar; Blastocystis sp. - wild rodents; Cryptosporidium spp. - wild fish; Encephalitozoon spp. - wild birds; Entamoeba spp. - non-human primates; Enterocytozoon bieneusi - wild cervids; Giardia duodenalis - red foxes; Sarcocystis nesbitti - snakes; Toxoplasma gondii - bobcats). Molecular tools have provided evidence that some enteric protozoa in wildlife may infect humans, but due to limited discriminatory power, often only the zoonotic potential of the parasite is indicated. Molecular analyses, which should be as discriminatory as possible, are one, but not the only, component of the toolbox for investigating potential public health impacts from pathogenic enteric protozoa in wildlife.
机译:新兴传染病通常是人畜共患病的,通常起源于野生动植物,但肠原生动物被认为是相对较小的病因。关于病原性肠原生动物是否可能在野生动植物和人类之间传播的观点已经由我们的调查工具形成,并引起了关于特定物种是否是人畜共患病或具有适应宿主生命周期的争论。当鉴定肠道原生动物的唯一方法是形态学时,可以假设许多肠道原生动物定居在多个宿主上,并且可能是人畜共患病的。当分子工具揭示出定植于人类和其他动物的形态相同物种的遗传差异时,宿主特异性似乎更可能出现。被发现具有与人宿主在形态学上无法区分的寄生虫的遗传上相同的动物寄生虫(在所研究的几个基因上)与形态上无法区分的寄生虫。现在,更多具有歧视性的分子工具再次细分了一些原生动物。同时,一些感染事件表明,在条件允许的情况下,某些“宿主特异性”原生动物实际上可以感染各种宿主。我们理解中的这些反复变化与可使用的调查工具有内在联系。在这里,我们回顾了分子工具如何帮助或有时混淆了我们对九种肠道原生动物和野生生物宿主(例如Balantoides coli-野猪; Blastocystis sp。-野鼠; Cryptosporidium spp。-野生鱼; Encephalitozoon)的公共健康威胁的理解。 spp。-野生鸟类; Entamoeba spp。-非人类灵长类; Enterocytozoon bieneusi-野生宫颈; Giardia duodenalis-赤狐; Sarcocystis nesbitti-蛇; Toxoplasma gondii-山猫)。分子工具已提供证据表明野生生物中的某些肠原生动物可能感染人类,但由于歧视能力有限,通常仅显示出该寄生虫的人畜共患病潜力。分子分析应尽可能具有区分性,是调查野生生物中病原性肠道原生动物潜在的公共健康影响的工具箱之一,但不是唯一的组成部分。

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