首页> 外文期刊>BioMed research international >Fitness Cost of Litomosoides sigmodontis FUarlal Infection In Mite Vectors; Implications of Infected Haematopfaagous Arthropod Excretory Products In Host-Vector Interactions
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Fitness Cost of Litomosoides sigmodontis FUarlal Infection In Mite Vectors; Implications of Infected Haematopfaagous Arthropod Excretory Products In Host-Vector Interactions

机译:螨载体中Litomosoides sigmodontis FUarlal感染的适应性成本;感染的血生节肢动物节肢排泄产物在宿主-载体相互作用中的意义

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摘要

Filariae are a leading cause of infections which are responsible for serious dermatological, ocular, and vascular lesions. Infective third stage larvae (L3) are transmitted through the bite of a haematophagous vector. Litomosoides sigmodontis is a well-established model of filariasis in the mouse, with the vector being the mite Ornithonyssus bacoti. The aim of the study was to analyse the filarial infection in mites to determine the consequences of filarial infection in the blood-feeding and the reproduction of mites as well as in the regulation of vector-induced inflammation in the mouse skin. Firstly, L3 are unevenly distributed throughout the host population and the majority of the population harbours a moderate infection (1 to 6 L3). Filarial infection does not significantly affect the probing delay for blood feeding. The number of released protonymphs is lower in infected mites but is not correlated with the L3 burden. Finally, induced excreted proteins from infected mites but not from uninfected mites stimulate TNF-a and the neutrophil-chemoattractant KC production by antigen-presenting cells (APCs). Altogether, these results describe the modification of the mite behavior under filarial infection and suggest that the immunomodulatory capacity of the mite may be modified by the presence of the parasite, hindering its defensive ability towards the vertebrate host.
机译:丝虫是引起严重皮肤病,眼和血管损伤的主要感染原因。感染性第三阶段幼虫(L3)通过食血载体的叮咬传播。 sigmodontis sigmodontis是小鼠中丝虫病的公认模型,载体为螨鸟杆菌。该研究的目的是分析螨虫中的丝虫感染,以确定丝虫感染在螨虫的采血和繁殖以及在媒介物诱导的小鼠皮肤炎症调节中的后果。首先,L3在整个寄居人口中分布不均,大多数人口中度感染(1至6 L3)。丝虫感染不会显着影响供血的探测延迟。在受感染的螨虫中,释放的质子淋巴的数量较少,但与L3负担无关。最后,从受感染的螨虫诱导的排泄蛋白,但未受感染的螨虫诱导的排泄蛋白,可刺激抗原呈递细胞(APC)刺激TNF-α和嗜中性白细胞趋化因子KC的产生。总而言之,这些结果描述了在丝虫感染下螨的行为的改变,并表明该寄生虫的存在可能改变了螨的免疫调节能力,从而阻碍了其对脊椎动物宿主的防御能力。

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