Comparative Community Ecology Reveals Conserved Ectoparasite Microbiomes Amidst Variable Host and Environment Microbiomes

The microbiome-the community of microorganisms that is associated with an individual animal-has been an important driver of insect biodiversity globally, enabling insects to specialize in narrow, nutrient-deficient diets. The importance of maternally inherited, obligate bacterial endosymbionts in provisioning nutrients missing from these narrow dietary niches has been well studied in insects. However, we know comparatively little about the processes that dictate the composition of non-maternally inherited bacteria in insect microbiomes, despite the importance of these bacteria in insect health, fitness, and vector competence. Here, we used two species of obligate insect ectoparasites of bats, the bat flies (Streblidae) <i>Trichobius sphaeronotus</i> and <i>Nycterophilia coxata</i>, to examine whether the microbiome, beyond obligate bacterial endosymbionts, is conserved or variable across geographic space, between ectoparasite species, or covaries with the external microbiome of their bat hosts or the cave environment. Our results indicate that ectoparasite microbiomes are highly conserved and specific to ectoparasite species, despite these species feeding on the blood of the same bat individuals in some cases. In contrast, we found high geographic variation in the fur microbiome of host bats and that the bat fur microbiome mimics the cave microbiomes. This research suggests that there is a constraint on blood-feeding insect ectoparasites to maintain a specific microbiome distinct from their host and the environment, potentially to meet their nutritional needs. Given that many of these bacteria are not known to be maternally inherited, this research lays the foundation for future examinations of how blood-feeding arthropods acquire and maintain bacteria in their microbiomes.

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Journal
Ecology and Evolution
Published
2025-04-01
DOI
https://doi.org/10.1002/ece3.71120
Citations
2
Primary Topic
Insect symbiosis and bacterial influences
Type
article
Field-Weighted Citation Impact
3.34

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article

Comparative Community Ecology Reveals Conserved Ectoparasite Microbiomes Amidst Variable Host and Environment Microbiomes

S. Sommer, Luis Víquez‐R, Ana M. Ibarra, Rodrigo A. Medellín et al.
2 citations
Ecology and Evolution
Insect symbiosis and bacterial influences
3.34
article

Comparative Community Ecology Reveals Conserved Ectoparasite Microbiomes Amidst Variable Host and Environment Microbiomes

S. Sommer, Luis Víquez‐R, Ana M. Ibarra, Rodrigo A. Medellín, Katharina Dittmar, Winifred F. Frick, Marco Tschapka, Nancy B. Simmons, Susan L. Perkins, Kelly A. Speer, Raisa Preciado, Ricardo Sánchez Calderón
article en
2 citations

Abstract

The microbiome-the community of microorganisms that is associated with an individual animal-has been an important driver of insect biodiversity globally, enabling insects to specialize in narrow, nutrient-deficient diets. The importance of maternally inherited, obligate bacterial endosymbionts in provisioning nutrients missing from these narrow dietary niches has been well studied in insects. However, we know comparatively little about the processes that dictate the composition of non-maternally inherited bacteria in insect microbiomes, despite the importance of these bacteria in insect health, fitness, and vector competence. Here, we used two species of obligate insect ectoparasites of bats, the bat flies (Streblidae) <i>Trichobius sphaeronotus</i> and <i>Nycterophilia coxata</i>, to examine whether the microbiome, beyond obligate bacterial endosymbionts, is conserved or variable across geographic space, between ectoparasite species, or covaries with the external microbiome of their bat hosts or the cave environment. Our results indicate that ectoparasite microbiomes are highly conserved and specific to ectoparasite species, despite these species feeding on the blood of the same bat individuals in some cases. In contrast, we found high geographic variation in the fur microbiome of host bats and that the bat fur microbiome mimics the cave microbiomes. This research suggests that there is a constraint on blood-feeding insect ectoparasites to maintain a specific microbiome distinct from their host and the environment, potentially to meet their nutritional needs. Given that many of these bacteria are not known to be maternally inherited, this research lays the foundation for future examinations of how blood-feeding arthropods acquire and maintain bacteria in their microbiomes.

Ecology and EvolutionVol. 15(4)
City College of New York (US), Bucknell University (US), American Museum of Natural History (US), City University of New York (US), University of California, Santa Cruz (US), Universität Ulm (DE), Northern Arizona University (US), Bat Conservation International (US), Universidad de Costa Rica (CR), Universidad de Sonora (MX), University at Buffalo, State University of New York (US), Universidad Nacional Autónoma de México (MX)
Rufford Foundation, Columbus Zoo and Aquarium, Elisabeth Kalko-Stiftung, Consejo Nacional de Ciencia y Tecnología, Universidad Nacional Autónoma de México
Openalex Percentile: Top 10%
Insect symbiosis and bacterial influences
3.34
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