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无脊椎动物模型反映了自然宿主内的致病潜力。

Invertebrate Model Mirrors the Pathogenic Potential of within the Natural Host.

作者信息

Burne Alexandra M, Richey Lauren J, Schoeb Trenton R, Brown Mary B

机构信息

Department of Infectious Disease and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, FL 32608, USA.

Comparative Pathology Services, Tufts University, Boston, MA 02155, USA.

出版信息

Transbound Emerg Dis. 2024 Mar 22;2024:3009838. doi: 10.1155/2024/3009838. eCollection 2024.

Abstract

Most mycoplasmal infections result in chronic, clinically silent disease. In direct contrast, elicits a fulminant, multisystem disease in the natural host, (American alligator). The goals of the study were to better understand the disease in the natural host and to determine if the invertebrate model could serve as a surrogate alternate host. The survival of alligators infected intratracheally was dose dependent (=0.0003), ranging from no mortality (10 CFU) to 100% mortality (10 CFU), with 60% mortality at the 10 and 10 CFU infectious dose. Microbial load in blood, joints, and brain was dose dependent, regardless of whether alligators were infected intratracheally or intravenously (  < 0.002). Weight loss was similarly impacted (  < 0.001). Experimental infection of the invertebrate mirrored the result in the natural host. In a dose response infection study, both larval survival curves and successful pupation curves were significantly different ( ≤ 0.0001) and dose dependent. Infected insects did not emerge as moths (  < 0.0001). Here, we describe the first study investigating as a surrogate model to assess the pathogenic potential of . survival was dose dependent and impacted life stage outcome.

摘要

大多数支原体感染会导致慢性、临床上无症状的疾病。与之形成直接对比的是,[病原体名称]在天然宿主美国短吻鳄中引发暴发性多系统疾病。本研究的目的是更好地了解天然宿主中的疾病情况,并确定无脊椎动物模型是否可作为替代宿主。经气管内感染的短吻鳄的存活率呈剂量依赖性(P = 0.0003),从无死亡(10 CFU)到100%死亡(10⁶ CFU)不等,在10⁴和10⁵ CFU感染剂量下死亡率为60%。血液、关节和大脑中的微生物载量呈剂量依赖性,无论短吻鳄是经气管内感染还是静脉内感染(P < 0.002)。体重减轻也受到类似影响(P < 0.001)。无脊椎动物[物种名称]的实验性感染反映了天然宿主中的结果。在剂量反应感染研究中,幼虫存活曲线和成功化蛹曲线均存在显著差异(P ≤ 0.0001)且呈剂量依赖性。受感染的昆虫未羽化为蛾(P < 0.0001)。在此,我们描述了第一项将[物种名称]作为替代模型来评估[病原体名称]致病潜力的研究。[物种名称]的存活呈剂量依赖性并影响生命阶段结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/12017031/5d2c25ee438c/TBED2024-3009838.001.jpg

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