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Ticks Ixodes scapularis Feed Repeatedly on White-Footed Mice despite Strong Inflammatory Response: An Expanding Paradigm for Understanding Tick–Host Interactions

机译:Strong虫肩cap突尽管有强烈的炎症反应但仍反复在白脚小鼠上进食:了解Understanding与宿主相互作用的扩展范式

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摘要

Ticks transmit infectious agents including bacteria, viruses and protozoa. However, their transmission may be compromised by host resistance to repeated tick feeding. Increasing host resistance to repeated tick bites is well known in laboratory animals, including intense inflammation at the bite sites. However, it is not known whether this also occurs in wild rodents such as white-footed mice, Peromyscus leucopus, and other wildlife, or if it occurs at all. According to the “host immune incompetence” hypothesis, if these mice do not have a strong inflammatory response, they would not reject repeated tick bites by Ixodes scapularis. To test this hypothesis, histopathological studies were done comparing dermal inflammation in P. leucopus versus guinea pigs, Cavia porcellus, repeatedly infested with I. scapularis. In P. leucopus, the immune cell composition was like that seen in laboratory mouse models, with some differences. However, there was a broad sessile lesion with intact dermal architecture, likely enabling the ticks to continue feeding unimpeded. In contrast, in C. porcellus, there was a relatively similar mixed cellular profile, but there also was a large, leukocyte-filled cavitary lesion and scab-like hyperkeratotic changes to the epidermal layer, along with itching and apparent pain. Ticks attached to sensitized C. porcellus fed poorly or were dislodged, presumably due to the weakened anchoring of the tick’s mouthparts cemented in the heavily inflamed and disintegrating dermal tissues. This is the first time that the architecture of the skin lesions has been recognized as a major factor in understanding tick–host tolerance versus tick bite rejection. These findings broadly strengthen previous work done on lab animal models but also help explain why I. scapularis can repeatedly parasitize white-footed mice, supporting the “immune evasion theory” but cannot repeatedly parasitize other, non-permissive hosts such as guinea pigs.
机译:cks传播传染病,包括细菌,病毒和原生动物。但是,它们的传播可能会因宿主对重复tick的抵抗而受到损害。在实验动物中,增加宿主对重复tick叮咬的抵抗力是众所周知的,包括叮咬部位的强烈炎症。但是,还不知道这种现象是否也发生在野生啮齿动物中,例如白脚小鼠,白皮病菌和其他野生动物,还是根本没有发生。根据“宿主免疫功能不全”假说,如果这些小鼠没有强烈的炎症反应,它们将不会拒绝肩x骨反复叮咬。为了验证这一假设,进行了组织病理学研究,比较了反复感染肩骨的白斑假单胞菌与豚鼠Cavia porcellus的皮肤炎症。在白斑假单胞菌中,免疫细胞组成类似于实验室小鼠模型中看到的,但有一些差异。然而,有一个完整的真皮结构的无蒂病变,很可能使壁虱能够不受阻碍地继续觅食。相比之下,在C. porcellus中,有一个相对相似的混合细胞分布,但是在表皮层上还有一个大的白细胞填充的空洞病变和sc样的过度角化变化,以及瘙痒和明显的疼痛。附着在致敏的梭状芽胞杆菌上的虫喂食不佳或被驱逐,可能是由于s虫的口器锚定在严重发炎和崩解的真皮组织中的固着力减弱。这是首次认识到皮损的结构是了解壁虱宿主耐受性与壁虱叮咬排斥的主要因素。这些发现在很大程度上增强了先前在实验室动物模型上所做的工作,但也有助于解释为什么肩I鱼可以反复寄生白脚小鼠,支持“免疫逃逸理论”,但不能反复寄生其他豚鼠等不允许的宿主。

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