Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats

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Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats. / Ingala, Melissa R.; Becker, Daniel J.; Holm, Jacob Bak; Kristiansen, Karsten; Simmons, Nancy B.

In: Ecology and Evolution, Vol. 9, No. 11, 2019, p. 6508-6523.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ingala, MR, Becker, DJ, Holm, JB, Kristiansen, K & Simmons, NB 2019, 'Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats', Ecology and Evolution, vol. 9, no. 11, pp. 6508-6523. https://doi.org/10.1002/ece3.5228

APA

Ingala, M. R., Becker, D. J., Holm, J. B., Kristiansen, K., & Simmons, N. B. (2019). Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats. Ecology and Evolution, 9(11), 6508-6523. https://doi.org/10.1002/ece3.5228

Vancouver

Ingala MR, Becker DJ, Holm JB, Kristiansen K, Simmons NB. Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats. Ecology and Evolution. 2019;9(11):6508-6523. https://doi.org/10.1002/ece3.5228

Author

Ingala, Melissa R. ; Becker, Daniel J. ; Holm, Jacob Bak ; Kristiansen, Karsten ; Simmons, Nancy B. / Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats. In: Ecology and Evolution. 2019 ; Vol. 9, No. 11. pp. 6508-6523.

Bibtex

@article{c1333bbd80b44e7d88fe36fda4a09d83,
title = "Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats",
abstract = "Host ecological factors and external environmental factors are known to influence the structure of gut microbial communities, but few studies have examined the impacts of environmental changes on microbiotas in free-ranging animals. Rapid land-use change has the potential to shift gut microbial communities in wildlife through exposure to novel bacteria and/or by changing the availability or quality of local food resources. The consequences of such changes to host health and fitness remain unknown and may have important implications for pathogen spillover between humans and wildlife. To better understand the consequences of land-use change on wildlife microbiotas, we analyzed long-term dietary trends, gut microbiota composition, and innate immune function in common vampire bats (Desmodus rotundus) in two nearby sites in Belize that vary in landscape structure. We found that vampire bats living in a small forest fragment had more homogenous diets indicative of feeding on livestock and shifts in microbiota heterogeneity, but not overall composition, compared to those living in an intact forest reserve. We also found that irrespective of sampling site, vampire bats which consumed relatively more livestock showed shifts in some core bacteria compared with vampire bats which consumed relatively less livestock. The relative abundance of some core microbiota members was associated with innate immune function, suggesting that future research should consider the role of the host microbiota in immune defense and its relationship to zoonotic infection dynamics. We suggest that subsequent homogenization of diet and habitat loss through livestock rearing in the Neotropics may lead to disruption to the microbiota that could have downstream impacts on host immunity and cross-species pathogen transmission.",
keywords = "Desmodus rotundus, diet homogenization, land-use change, livestock, microbiota, resource provisioning",
author = "Ingala, {Melissa R.} and Becker, {Daniel J.} and Holm, {Jacob Bak} and Karsten Kristiansen and Simmons, {Nancy B.}",
year = "2019",
doi = "10.1002/ece3.5228",
language = "English",
volume = "9",
pages = "6508--6523",
journal = "Ecology and Evolution",
issn = "2045-7758",
publisher = "Wiley",
number = "11",

}

RIS

TY - JOUR

T1 - Habitat fragmentation is associated with dietary shifts and microbiota variability in common vampire bats

AU - Ingala, Melissa R.

AU - Becker, Daniel J.

AU - Holm, Jacob Bak

AU - Kristiansen, Karsten

AU - Simmons, Nancy B.

PY - 2019

Y1 - 2019

N2 - Host ecological factors and external environmental factors are known to influence the structure of gut microbial communities, but few studies have examined the impacts of environmental changes on microbiotas in free-ranging animals. Rapid land-use change has the potential to shift gut microbial communities in wildlife through exposure to novel bacteria and/or by changing the availability or quality of local food resources. The consequences of such changes to host health and fitness remain unknown and may have important implications for pathogen spillover between humans and wildlife. To better understand the consequences of land-use change on wildlife microbiotas, we analyzed long-term dietary trends, gut microbiota composition, and innate immune function in common vampire bats (Desmodus rotundus) in two nearby sites in Belize that vary in landscape structure. We found that vampire bats living in a small forest fragment had more homogenous diets indicative of feeding on livestock and shifts in microbiota heterogeneity, but not overall composition, compared to those living in an intact forest reserve. We also found that irrespective of sampling site, vampire bats which consumed relatively more livestock showed shifts in some core bacteria compared with vampire bats which consumed relatively less livestock. The relative abundance of some core microbiota members was associated with innate immune function, suggesting that future research should consider the role of the host microbiota in immune defense and its relationship to zoonotic infection dynamics. We suggest that subsequent homogenization of diet and habitat loss through livestock rearing in the Neotropics may lead to disruption to the microbiota that could have downstream impacts on host immunity and cross-species pathogen transmission.

AB - Host ecological factors and external environmental factors are known to influence the structure of gut microbial communities, but few studies have examined the impacts of environmental changes on microbiotas in free-ranging animals. Rapid land-use change has the potential to shift gut microbial communities in wildlife through exposure to novel bacteria and/or by changing the availability or quality of local food resources. The consequences of such changes to host health and fitness remain unknown and may have important implications for pathogen spillover between humans and wildlife. To better understand the consequences of land-use change on wildlife microbiotas, we analyzed long-term dietary trends, gut microbiota composition, and innate immune function in common vampire bats (Desmodus rotundus) in two nearby sites in Belize that vary in landscape structure. We found that vampire bats living in a small forest fragment had more homogenous diets indicative of feeding on livestock and shifts in microbiota heterogeneity, but not overall composition, compared to those living in an intact forest reserve. We also found that irrespective of sampling site, vampire bats which consumed relatively more livestock showed shifts in some core bacteria compared with vampire bats which consumed relatively less livestock. The relative abundance of some core microbiota members was associated with innate immune function, suggesting that future research should consider the role of the host microbiota in immune defense and its relationship to zoonotic infection dynamics. We suggest that subsequent homogenization of diet and habitat loss through livestock rearing in the Neotropics may lead to disruption to the microbiota that could have downstream impacts on host immunity and cross-species pathogen transmission.

KW - Desmodus rotundus

KW - diet homogenization

KW - land-use change

KW - livestock

KW - microbiota

KW - resource provisioning

U2 - 10.1002/ece3.5228

DO - 10.1002/ece3.5228

M3 - Journal article

C2 - 31236240

AN - SCOPUS:85065656527

VL - 9

SP - 6508

EP - 6523

JO - Ecology and Evolution

JF - Ecology and Evolution

SN - 2045-7758

IS - 11

ER -

ID: 225998611