Journal
FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.868575
Keywords
Coxiella; symbiont; Rhipicephalus microplus; transcriptome; microbiome; tick
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Funding
- Conselho Nacional de Desenvolvimento Tecnologico-CNPq
- Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-CAPES
- INCT-Entomologia Molecular, Brazil
- Intramural Research Program of the National Institute of Allergy and Infectious Diseases [Z01 AI001337-01]
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Metagenomic studies have shown that bacteria and arthropods, including ticks, have widespread interactions, including symbiotic interactions. In this study, the absence of the mutualist endosymbiont CERM in R. microplus larvae led to changes in gene expression, specifically in genes involved in blood feeding capacity and extracellular matrix remodeling. These changes may explain the developmental blockage at the metanymph stage and reveal new physiological aspects of the symbiont-tick-vertebrate host interaction.
In the past decade, metagenomics studies exploring tick microbiota have revealed widespread interactions between bacteria and arthropods, including symbiotic interactions. Functional studies showed that obligate endosymbionts contribute to tick biology, affecting reproductive fitness and molting. Understanding the molecular basis of the interaction between ticks and their mutualist endosymbionts may help to develop control methods based on microbiome manipulation. Previously, we showed that Rhipicephalus microplus larvae with reduced levels of Coxiella endosymbiont of R. microplus (CERM) were arrested at the metanymph life stage (partially engorged nymph) and did not molt into adults. In this study, we performed a transcriptomic differential analysis of the R. microplus metanymph in the presence and absence of its mutualist endosymbiont. The lack of CERM resulted in an altered expression profile of transcripts from several functional categories. Gene products such as DA-P36, protease inhibitors, metalloproteases, and evasins, which are involved in blood feeding capacity, were underexpressed in CERM-free metanymphs. Disregulation in genes related to extracellular matrix remodeling was also observed in the absence of the symbiont. Taken together, the observed alterations in gene expression may explain the blockage of development at the metanymph stage and reveal a novel physiological aspect of the symbiont-tick-vertebrate host interaction.
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