Bowen Lizabeth, Manlove Kezia, Roug Annette, Waters Shannon, LaHue Nate, Wolff Peregrine
U.S. Geological Survey, Western Ecological Research Center, Davis, CA, 95616, USA.
Department of Wildland Resources and Ecology Center, Utah State University, Logan, UT, 84322, USA.
Conserv Physiol. 2022 Jul 3;10(1):coac046. doi: 10.1093/conphys/coac046. eCollection 2022.
Increasing risk of pathogen spillover coupled with overall declines in wildlife population abundance in the Anthropocene make infectious disease a relevant concern for species conservation worldwide. While emerging molecular tools could improve our diagnostic capabilities and give insight into mechanisms underlying wildlife disease risk, they have rarely been applied in practice. Here, employing a previously reported gene transcription panel of common immune markers to track physiological changes, we present a detailed analysis over the course of both acute and chronic infection in one wildlife species where disease plays a critical role in conservation, bighorn sheep (). Differential gene transcription patterns distinguished between infection statuses over the course of acute infection and differential correlation (DC) analyses identified clear changes in gene co-transcription patterns over the early stages of infection, with transcription of four genes-TGFb, AHR, IL1b and MX1-continuing to increase even as transcription of other immune-associated genes waned. In a separate analysis, we considered the capacity of the same gene transcription panel to aid in differentiating between chronically infected animals and animals in other disease states outside of acute disease events (an immediate priority for wildlife management in this system). We found that this transcription panel was capable of accurately identifying chronically infected animals in the test dataset, though additional data will be required to determine how far this ability extends. Taken together, our results showcase the successful proof of concept and breadth of potential utilities that gene transcription might provide to wildlife disease management, from direct insight into mechanisms associated with differential disease response to improved diagnostic capacity in the field.
在人类世,病原体溢出风险增加,再加上野生动物种群数量总体下降,使传染病成为全球物种保护的一个相关问题。虽然新兴的分子工具可以提高我们的诊断能力,并深入了解野生动物疾病风险背后的机制,但它们在实践中很少被应用。在这里,我们利用先前报道的一组常见免疫标志物的基因转录面板来追踪生理变化,对一种疾病在保护中起关键作用的野生动物——大角羊,进行了急性和慢性感染过程的详细分析。在急性感染过程中,不同的基因转录模式区分了感染状态,差异相关性(DC)分析确定了感染早期基因共转录模式的明显变化,即使其他免疫相关基因的转录减弱,四个基因——转化生长因子β(TGFb)、芳烃受体(AHR)、白细胞介素1β(IL1b)和Mx1蛋白(MX1)的转录仍持续增加。在另一项分析中,我们考虑了同一基因转录面板在区分慢性感染动物和急性疾病事件之外的其他疾病状态的动物方面的能力(这是该系统中野生动物管理的当务之急)。我们发现,这个转录面板能够在测试数据集中准确识别慢性感染动物,不过还需要更多数据来确定这种能力的适用范围。总之,我们的结果展示了基因转录在野生动物疾病管理方面可能提供的概念验证的成功以及潜在效用的广度,从直接洞察与不同疾病反应相关的机制到提高现场诊断能力。