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The Tick Endosymbiont Candidatus Midichloria Mitochondrii and Selenoproteins Are Essential for the Growth of Rickettsia Parkeri in the Gulf Coast Tick Vector

Overview
Journal Microbiome
Publisher Biomed Central
Specialties Genetics
Microbiology
Date 2018 Aug 15
PMID 30103809
Citations 53
Authors
Affiliations
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Abstract

Background: Pathogen colonization inside tick tissues is a significant aspect of the overall competence of a vector. Amblyomma maculatum is a competent vector of the spotted fever group rickettsiae, Rickettsia parkeri. When R. parkeri colonizes its tick host, it has the opportunity to dynamically interact with not just its host but with the endosymbionts living within it, and this enables it to modulate the tick's defenses by regulating tick gene expression. The microbiome in A. maculatum is dominated by two endosymbiont microbes: a Francisella-like endosymbiont (FLE) and Candidatus Midichloria mitochondrii (CMM). A range of selenium-containing proteins (selenoproteins) in A. maculatum ticks protects them from oxidative stress during blood feeding and pathogen infections. Here, we investigated rickettsial multiplication in the presence of tick endosymbionts and characterized the functional significance of selenoproteins during R. parkeri replication in the tick.

Results: FLE and CMM were quantified throughout the tick life stages by quantitative PCR in R. parkeri-infected and uninfected ticks. R. parkeri infection was found to decrease the FLE numbers but CMM thrived across the tick life cycle. Our qRT-PCR analysis indicated that the transcripts of genes with functions related to redox (selenogenes) were upregulated in ticks infected with R. parkeri. Three differentially expressed proteins, selenoprotein M, selenoprotein O, and selenoprotein S were silenced to examine their functional significance during rickettsial replication within the tick tissues. Gene silencing of the target genes was found to impair R. parkeri colonization in the tick vector. Knockdown of the selenogenes triggered a compensatory response from other selenogenes, as observed by changes in gene expression, but oxidative stress levels and endoplasmic reticulum stress inside the ticks were also found to have heightened.

Conclusions: This study illustrates the potential of this new research model for augmenting our understanding of the pathogen interactions occurring within tick hosts and the important roles that symbionts and various tick factors play in regulating pathogen growth.

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References
1.
Paddock C, Goddard J . The Evolving Medical and Veterinary Importance of the Gulf Coast tick (Acari: Ixodidae). J Med Entomol. 2015; 52(2):230-52. DOI: 10.1093/jme/tju022. View

2.
Wright C, Gaff H, Sonenshine D, Hynes W . Experimental vertical transmission of Rickettsia parkeri in the Gulf Coast tick, Amblyomma maculatum. Ticks Tick Borne Dis. 2015; 6(5):568-73. DOI: 10.1016/j.ttbdis.2015.04.011. View

3.
Ahantarig A, Trinachartvanit W, Baimai V, Grubhoffer L . Hard ticks and their bacterial endosymbionts (or would be pathogens). Folia Microbiol (Praha). 2013; 58(5):419-28. DOI: 10.1007/s12223-013-0222-1. View

4.
Hughes G, Rivero A, Rasgon J . Wolbachia can enhance Plasmodium infection in mosquitoes: implications for malaria control?. PLoS Pathog. 2014; 10(9):e1004182. PMC: 4154766. DOI: 10.1371/journal.ppat.1004182. View

5.
Epis S, Sassera D, Beninati T, Lo N, Beati L, Piesman J . Midichloria mitochondrii is widespread in hard ticks (Ixodidae) and resides in the mitochondria of phylogenetically diverse species. Parasitology. 2008; 135(4):485-94. DOI: 10.1017/S0031182007004052. View