Literature DB >> 33451085

Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity.

Marah Stoldt1, Linda Klein1, Sara Beros2, Falk Butter3, Evelien Jongepier4, Barbara Feldmeyer5, Susanne Foitzik1.   

Abstract

Most species are either parasites or exploited by parasites, making parasite-host interactions a driver of evolution. Parasites with complex life cycles often evolve strategies to facilitate transmission to the definitive host by manipulating their intermediate host. Such manipulations could explain phenotypic changes in the ant Temnothorax nylanderi, the intermediate host of the cestode Anomotaenia brevis. In addition to behavioral and morphological alterations, infected workers exhibit prolonged lifespans, comparable to that of queens, which live up to two decades. We used transcriptomic data from cestodes and ants of different castes and infection status to investigate the molecular underpinnings of phenotypic alterations in infected workers and explored whether the extended lifespan of queens and infected workers has a common molecular basis. Infected workers and queens commonly upregulated only six genes, one of them with a known anti-aging function. Both groups overexpressed immune genes, although not the same ones. Our findings suggest that the lifespan extension of infected workers is not achieved via the expression of queen-specific genes. The analysis of the cestodes' transcriptome revealed dominant expression of genes of the mitochondrial respiratory transport chain, which indicates an active metabolism and shedding light on the physiology of the parasite in its cysticercoid stage.

Entities:  

Keywords:  Anomotaenia brevis; Hymenoptera; Temnothorax nylanderi; extended phenotype; host lifespan; host–parasite interaction; transcriptomics

Year:  2021        PMID: 33451085      PMCID: PMC7828512          DOI: 10.3390/genes12010095

Source DB:  PubMed          Journal:  Genes (Basel)        ISSN: 2073-4425            Impact factor:   4.096


  70 in total

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