Vermeulen Sophia, Forsman Anna M, de Bekker Charissa
Department of Biology, University of Central Florida, Orlando FL 32816, USA.
Department of Biology, Colby University, Waterville ME 04901, USA.
Curr Res Insect Sci. 2024 Nov 30;7:100102. doi: 10.1016/j.cris.2024.100102. eCollection 2025.
The bacterial microbiome of the ant has been well characterized across body regions and maturation levels. However, potential effects of entomopathogens on the gut microbiome, and the fungal communities therein, are yet to be assessed. Additionally, the mycobiome remains often overlooked despite playing a vital role in gut ecology with potential implications for health and infection outcomes. We characterized the effects of two entomopathogens with different infection strategies on the gut micro- and mycobiota of over time; and Specialist, 'zombie-making' fungi hijack the behavior of ants over three weeks, leading them to find an elevated position and fix themselves in place with their mandibles. This summiting behavior is adaptive to as the ant transports the fungus to conditions that favor fruiting body development, spore production, dispersal, and transmission. In contrast, the generalist entomopathogen infects and kills the ant within a few days, without the induction of obvious fungus-adaptive behaviors. By comparing healthy ants with and infected ants we aimed to 1) describe the dynamics of the micro- and mycobiome of during infection and 2) determine if the effects on gut microbiota are distinctive between fungi that have different infection strategies. While did not measurably affect the ant host micro-and mycobiome, did, especially for the mycobiome. Moreover, ants that were sampled during -adaptive summiting behavior had a significantly different micro- and mycobiome composition compared to healthy controls and those sampled before and after manipulation took place. This suggests that the host microbiome might have a role to play in the manipulation strategy of .
蚂蚁的细菌微生物群已在不同身体区域和成熟水平上得到了充分表征。然而,昆虫病原体对肠道微生物群及其内部真菌群落的潜在影响尚未得到评估。此外,尽管真菌微生物群在肠道生态中起着至关重要的作用,对健康和感染结果可能有影响,但它仍然常常被忽视。我们表征了两种具有不同感染策略的昆虫病原体随时间对蚂蚁肠道微生物群和真菌微生物群的影响;以及专性的“制造僵尸”真菌在三周多的时间里控制蚂蚁的行为,使它们找到一个较高的位置并用下颚固定在那里。这种登高行为对[真菌名称]是适应性的,因为蚂蚁将真菌带到有利于子实体发育、孢子产生、传播和扩散的条件下。相比之下,泛性昆虫病原体在几天内感染并杀死蚂蚁,不会诱导明显的真菌适应性行为。通过将健康蚂蚁与[真菌名称1]和[真菌名称2]感染的蚂蚁进行比较,我们旨在:1)描述感染期间[蚂蚁名称]肠道微生物群和真菌微生物群的动态变化;2)确定对肠道微生物群的影响在具有不同感染策略的真菌之间是否有差异。虽然[真菌名称1]对蚂蚁宿主的微生物群和真菌微生物群没有可测量的影响,但[真菌名称2]有影响,尤其是对真菌微生物群。此外,在[真菌名称2]适应性登高行为期间采样的蚂蚁,其微生物群和真菌微生物群组成与健康对照组以及在操作前后采样的蚂蚁相比有显著差异。这表明宿主微生物群可能在[真菌名称2]的控制策略中发挥作用。