Villar Margarita, Popara Marina, Ayllón Nieves, Fernández de Mera Isabel G, Mateos-Hernández Lourdes, Galindo Ruth C, Manrique Marina, Tobes Raquel, de la Fuente José
SaBio. Instituto de Investigación en Recursos Cinegéticos IREC-CSIC-UCLM-JCCM, Ciudad Real, Spain.
Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, Oklahoma, United States of America.
PLoS One. 2014 Feb 21;9(2):e89564. doi: 10.1371/journal.pone.0089564. eCollection 2014.
Dermacentor reticulatus (Fabricius, 1794) is distributed in Europe and Asia where it infests and transmits disease-causing pathogens to humans, pets and other domestic and wild animals. However, despite its role as a vector of emerging or re-emerging diseases, very little information is available on the genome, transcriptome and proteome of D. reticulatus. Tick larvae are the first developmental stage to infest hosts, acquire infection and transmit pathogens that are transovarially transmitted and are exposed to extremely stressing conditions. In this study, we used a systems biology approach to get an insight into the mechanisms active in D. reticulatus unfed larvae, with special emphasis on stress response.
The results support the use of paired end RNA sequencing and proteomics informed by transcriptomics (PIT) for the analysis of transcriptomics and proteomics data, particularly for organisms such as D. reticulatus with little sequence information available. The results showed that metabolic and cellular processes involved in protein synthesis were the most active in D. reticulatus unfed larvae, suggesting that ticks are very active during this life stage. The stress response was activated in D. reticulatus unfed larvae and a Rickettsia sp. similar to R. raoultii was identified in these ticks.
The activation of stress responses in D. reticulatus unfed larvae likely counteracts the negative effect of temperature and other stress conditions such as Rickettsia infection and favors tick adaptation to environmental conditions to increase tick survival. These results show mechanisms that have evolved in D. reticulatus ticks to survive under stress conditions and suggest that these mechanisms are conserved across hard tick species. Targeting some of these proteins by vaccination may increase tick susceptibility to natural stress conditions, which in turn reduce tick survival and reproduction, thus reducing tick populations and vector capacity for tick-borne pathogens.
网纹革蜱(Dermacentor reticulatus,Fabricius,1794)分布于欧洲和亚洲,它会叮咬人类、宠物及其他家养和野生动物并传播致病病原体。然而,尽管其作为新出现或再次出现疾病的传播媒介,关于网纹革蜱的基因组、转录组和蛋白质组的信息却非常少。蜱幼虫是侵染宿主、感染病原体并传播经卵传递病原体的第一个发育阶段,且会暴露于极端应激条件下。在本研究中,我们采用系统生物学方法来深入了解未进食的网纹革蜱幼虫中活跃的机制,特别关注应激反应。
结果支持使用双末端RNA测序和转录组学指导的蛋白质组学(PIT)来分析转录组学和蛋白质组学数据,尤其是对于像网纹革蜱这样序列信息很少的生物。结果表明,参与蛋白质合成的代谢和细胞过程在未进食的网纹革蜱幼虫中最为活跃,这表明蜱在这个生命阶段非常活跃。未进食的网纹革蜱幼虫中应激反应被激活,并且在这些蜱中鉴定出一种与拉乌尔立克次体(R. raoultii)相似的立克次体属(Rickettsia sp.)。
未进食的网纹革蜱幼虫中应激反应的激活可能抵消温度和其他应激条件(如立克次体感染)的负面影响,并有利于蜱适应环境条件以提高蜱的存活率。这些结果显示了网纹革蜱为在应激条件下生存而进化出的机制,并表明这些机制在硬蜱物种中是保守的。通过疫苗接种靶向其中一些蛋白质可能会增加蜱对自然应激条件的易感性,进而降低蜱的存活率和繁殖率,从而减少蜱的数量和蜱传播病原体的媒介能力。