scholarly journals Male Age and Wolbachia Dynamics: Investigating How Fast and Why Bacterial Densities and Cytoplasmic Incompatibility Strengths Vary

mBio ◽  
2021 ◽  
Author(s):  
J. Dylan Shropshire ◽  
Emily Hamant ◽  
Brandon S. Cooper

Wolbachia bacteria are the most common animal-associated endosymbionts due in large part to their manipulation of host reproduction. Many Wolbachia cause cytoplasmic incompatibility (CI) that kills uninfected host eggs.

2002 ◽  
Vol 80 (2) ◽  
pp. 79-87 ◽  
Author(s):  
K. TRACY REYNOLDS ◽  
ARY A. HOFFMANN

In Drosophila melanogaster, the maternally inherited endocellular microbe Wolbachia causes cytoplasmic incompatibility (CI) in crosses between infected males and uninfected females. CI results in a reduction in the number of eggs that hatch. The level of CI expression in this species has been reported as varying from partial (a few eggs fail to hatch) to nonexistent (all eggs hatch). We show that male age in this host species has a large impact on the level of CI exhibited and explains much of this variability. Strong CI is apparent when young males are used in crosses. CI declines rapidly with male age, particularly when males are repeatedly mated. Wolbachia from a Canton S line that was previously reported as not causing CI does in fact induce CI when young males are used in crosses, albeit at a weaker level than in other D. melanogaster strains. The strain differences in CI expression are due to host background effects rather than differences in Wolbachia strains. These results highlight the importance of undertaking crosses with a range of male ages and nuclear backgrounds before ascribing particular host phenotypes to Wolbachia strains.


2021 ◽  
Author(s):  
John Dylan Shropshire ◽  
Emily Hamant ◽  
Brandon S Cooper

Endosymbiotic Wolbachia bacteria infect divergent arthropod and nematode hosts. Many strains cause cytoplasmic incompatibility (CI) that kills uninfected embryos fertilized by Wolbachia-modified sperm. Infected embryos are protected from CI, promoting Wolbachia spread to high equilibrium frequencies balanced by imperfect maternal transmission. CI strength varies widely in nature and tends to decrease as males age. Understanding the causes of CI-strength variation is crucial to explain Wolbachia prevalence in host populations. Here, we investigate how fast and why CI strength decreases with male age in two model systems: wMel in Drosophila melanogaster and wRi in D. simulans. Average wMel CI strength decreases rapidly (19%/ day), and wRi CI strength decreases slowly (6%/ day) as males age; thus, within three days, wMel-infected males do not cause CI, whereas twelve-day-old wRi-infected males still cause minor, yet significant, CI. We tested if reductions in Wolbachia densities or CI gene expression as males age could explain this pattern. Indeed, wRi densities and CI gene expression decrease in testes as males age, but wMel densities and CI gene expression surprisingly increase with male age as CI strength decreases. Phage WO lytic activity and wMel Octomom copy number-an ampliconic gene region that influences wMel proliferation-do not explain age-dependent Wolbachia densities. However, the expression of Relish, an essential gene in the Drosophila immune deficiency pathway, strongly correlates with wMel densities. Together, these results suggest that testes-wide Wolbachia density and CI gene expression are insufficient to explain age-dependent CI strength across strains and that Wolbachia density is variably impacted by male age across Wolbachia-host associations. We hypothesize that host immunity may underlie variation in age-dependent density dynamics. More broadly, the rapid decline of wMel CI strength during the first week of D. melanogaster life likely contributes to wMel frequency variation observed on several continents.


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