Phylogeny, morphology, virulence, ecology, and host range of Ordospora pajunii (Ordosporidae), a microsporidian symbiont of Daphnia spp

The impacts of microsporidia on host individuals are frequently subtle and can be context dependent. A key example of the latter comes from a recently discovered microsporidian symbiont of , the net impact of which was found to shift from negative to positive based on environmental context. Given th...

Full description

Saved in:
Bibliographic Details
Published in:mBio Vol. 15; no. 6; p. e0058224
Main Authors: Dziuba, Marcin K, McIntire, Kristina M, Seto, Kensuke, Davenport, Elizabeth S, Rogalski, Mary A, Gowler, Camden D, Baird, Emma, Vaandrager, Megan, Huerta, Cristian, Jaye, Riley, Corcoran, Fiona E, Withrow, Alicia, Ahrendt, Steven, Salamov, Asaf, Nolan, Matt, Tejomurthula, Sravanthi, Barry, Kerrie, Grigoriev, Igor V, James, Timothy Y, Duffy, Meghan A
Format: Journal Article
Language:English
Published: United States American Society for Microbiology 23-04-2024
American Society for Microbiology (ASM)
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The impacts of microsporidia on host individuals are frequently subtle and can be context dependent. A key example of the latter comes from a recently discovered microsporidian symbiont of , the net impact of which was found to shift from negative to positive based on environmental context. Given this, we hypothesized low baseline virulence of the microsporidian; here, we investigated the impact of infection on hosts in controlled conditions and the absence of other stressors. We also investigated its phylogenetic position, ecology, and host range. The genetic data indicate that the symbiont is , a newly described microsporidian parasite of . We show that infection damages the gut, causing infected epithelial cells to lose microvilli and then rupture. The prevalence of this microsporidian could be high (up to 100% in the lab and 77% of adults in the field). Its overall virulence was low in most cases, but some genotypes suffered reduced survival and/or reproduction. Susceptibility and virulence were strongly host-genotype dependent. We found that North American were able to infect multiple species, including the European species , as well as spp. Given the low, often undetectable virulence of this microsporidian and potentially far-reaching consequences of infections for the host when interacting with other pathogens or food, this symbiosis emerges as a valuable system for studying the mechanisms of context-dependent shifts between mutualism and parasitism, as well as for understanding how symbionts might alter host interactions with resources. The net outcome of symbiosis depends on the costs and benefits to each partner. Those can be context dependent, driving the potential for an interaction to change between parasitism and mutualism. Understanding the baseline fitness impact in an interaction can help us understand those shifts; for an organism that is generally parasitic, it should be easier for it to become a mutualist if its baseline virulence is relatively low. Recently, a microsporidian was found to become beneficial to its hosts in certain ecological contexts, but little was known about the symbiont (including its species identity). Here, we identify it as the microsporidium . Despite the parasitic nature of microsporidia, we found to be, at most, mildly virulent; this helps explain why it can shift toward mutualism in certain ecological contexts and helps establish is a valuable model for investigating shifts along the mutualism-parasitism continuum.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
USDOE
Gordon and Betty Moore Foundation (GBMF)
National Science Foundation (NSF)
AC02-05CH11231; DEB-1305836; DEB-1748729; GBMF9202; DEB-1929738
USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science (BSS)
The authors declare no conflict of interest.
ISSN:2150-7511
2150-7511
DOI:10.1128/mbio.00582-24