猫蚤消化道IMD信号通路的转录诱导及其抗菌活性

IF 3 2区 医学 Q1 PARASITOLOGY
Katie Weber, Dhruva Karnik, Lisa D Brown
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引用次数: 0

摘要

背景:跳蚤是传播几种革兰氏阴性细菌病原体的昆虫媒介,通过摄入受感染的脊椎动物血液获得。为了对抗食源性疾病,昆虫中肠上皮细胞具有有效的微生物识别和控制系统,例如调节抗菌肽(AMPs)表达的免疫缺陷(IMD)途径。然而,尽管它们在医学和兽医方面具有重要意义,但人们对猫蚤(Ctenocephalides felis)消化道中IMD信号通路和amp产生的了解相对较少。方法:在本研究中,我们在暴露于三种不同细菌(革兰氏阴性亨塞巴尔通菌(一种蚤传病原体)、革兰氏阴性粘质沙雷氏菌(一种实验室模型物种)和革兰氏阳性黄体微球菌(一种实验室模型物种)后,测量了猫C. felis消化道中包含IMD途径的靶基因以及相应的AMP转录物的表达。此外,我们检测了体外细菌攻击后和成虫羽化后不同天数从跳蚤消化道分离的蛋白质的抗菌活性,以确定喂养诱导的抗菌活性是否随年龄而变化。结果:在我们对C. felis的分析中,我们观察到代表性IMD通路基因和相关AMP转录物的表达增加,表明IMD通路被激活。此外,我们的研究结果显示,不同的细菌物种引发了不同的IMD途径基因的转录谱,表明对细菌入侵的物种特异性反应。我们发现猫梭菌的肠道产生抗菌分子作为一种局部防御机制。此外,我们观察到具有抗菌特性的蛋白质是肠道局部防御机制的一部分,其抗菌活性模式与感染状态和年龄有关。结论:我们的研究结果为猫蚤调节消化道中针对不同细菌的免疫反应的潜在机制提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional induction of the IMD signaling pathway and associated antibacterial activity in the digestive tract of cat fleas (Ctenocephalides felis).

Background: Fleas are insect vectors that transmit several Gram-negative bacterial pathogens acquired by ingesting infected vertebrate blood. To combat foodborne illness, insect midgut epithelial cells are armed with efficient microbial recognition and control systems, such as the immune deficiency (IMD) pathway that regulates the expression of antimicrobial peptides (AMPs). However, despite their medical and veterinary importance, relatively little is known about the IMD signaling pathway and production of AMPs in the digestive tract of cat fleas (Ctenocephalides felis).

Methods: In the present study, we measured the expression of target genes comprising the IMD pathway, as well as corresponding AMP transcripts, in the digestive tract of C. felis following exposure to three different species of bacteria: Gram-negative Bartonella henselae (a flea-borne pathogen), Gram-negative Serratia marcescens (a model laboratory species), and Gram-positive Micrococcus luteus (a model laboratory species). Additionally, we examined the antibacterial activity of proteins isolated from the flea digestive tract in vitro following bacterial challenge and at different days post adult emergence to determine if feeding-induced antibacterial activity varies with age.

Results: In our analysis of C. felis, we observed an increase in the expression of representative IMD pathway genes and associated AMP transcripts, indicating the activation of the IMD pathway. Furthermore, our results revealed that different bacterial species elicit distinct transcriptional profiles of IMD pathway genes, suggesting a species-specific response to bacterial invasion. We found that the gut of C. felis produces antibacterial molecules as a localized defense mechanism. Additionally, we observed that proteins with antimicrobial properties are synthesized as part of local defense mechanisms in the gut, with differential patterns of antibacterial activity related to infection status and age.

Conclusions: Our findings provide essential insights into the potential mechanisms by which cat fleas regulate immune responses in their digestive tract against different bacterial species.

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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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