The gut bacterial community affects immunity but not metabolism in a specialist herbivorous butterfly
(2020) In Ecology and Evolution 10(16). p.8755-8769- Abstract
Plant tissues often lack essential nutritive elements and may contain a range of secondary toxic compounds. As nutritional imbalance in food intake may affect the performances of herbivores, the latter have evolved a variety of physiological mechanisms to cope with the challenges of digesting their plant-based diet. Some of these strategies involve living in association with symbiotic microbes that promote the digestion and detoxification of plant compounds or supply their host with essential nutrients missing from the plant diet. In Lepidoptera, a growing body of evidence has, however, recently challenged the idea that herbivores are nutritionally dependent on their gut microbial community. It is suggested that many of the herbivorous... (More)
Plant tissues often lack essential nutritive elements and may contain a range of secondary toxic compounds. As nutritional imbalance in food intake may affect the performances of herbivores, the latter have evolved a variety of physiological mechanisms to cope with the challenges of digesting their plant-based diet. Some of these strategies involve living in association with symbiotic microbes that promote the digestion and detoxification of plant compounds or supply their host with essential nutrients missing from the plant diet. In Lepidoptera, a growing body of evidence has, however, recently challenged the idea that herbivores are nutritionally dependent on their gut microbial community. It is suggested that many of the herbivorous Lepidopteran species may not host a resident microbial community, but rather a transient one, acquired from their environment and diet. Studies directly testing these hypotheses are however scarce and come from an even more limited number of species. By coupling comparative metabarcoding, immune gene expression, and metabolomics analyses with experimental manipulation of the gut microbial community of prediapause larvae of the Glanville fritillary butterfly (Melitaea cinxia, L.), we tested whether the gut microbial community supports early larval growth and survival, or modulates metabolism or immunity during early stages of development. We successfully altered this microbiota through antibiotic treatments and consecutively restored it through fecal transplants from conspecifics. Our study suggests that although the microbiota is involved in the up-regulation of an antimicrobial peptide, it did not affect the life history traits or the metabolism of early instars larvae. This study confirms the poor impact of the microbiota on diverse life history traits of yet another Lepidoptera species. However, it also suggests that potential eco-evolutionary host-symbiont strategies that take place in the gut of herbivorous butterfly hosts might have been disregarded, particularly how the microbiota may affect the host immune system homeostasis.
(Less)
- author
- Duplouy, Anne LU ; Minard, Guillaume and Saastamoinen, Marjo
- organization
- publishing date
- 2020-08
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- antibiotic treatment, gut microbial community, immunity, larval development, larval survival, metabolites
- in
- Ecology and Evolution
- volume
- 10
- issue
- 16
- pages
- 15 pages
- publisher
- Wiley-Blackwell
- external identifiers
-
- pmid:32884655
- scopus:85088034282
- ISSN
- 2045-7758
- DOI
- 10.1002/ece3.6573
- language
- English
- LU publication?
- yes
- id
- 61142b02-3d39-49f6-b269-29f753f95d5c
- date added to LUP
- 2020-07-30 12:43:00
- date last changed
- 2024-06-26 19:53:08
@article{61142b02-3d39-49f6-b269-29f753f95d5c,
abstract = {{<p>Plant tissues often lack essential nutritive elements and may contain a range of secondary toxic compounds. As nutritional imbalance in food intake may affect the performances of herbivores, the latter have evolved a variety of physiological mechanisms to cope with the challenges of digesting their plant-based diet. Some of these strategies involve living in association with symbiotic microbes that promote the digestion and detoxification of plant compounds or supply their host with essential nutrients missing from the plant diet. In Lepidoptera, a growing body of evidence has, however, recently challenged the idea that herbivores are nutritionally dependent on their gut microbial community. It is suggested that many of the herbivorous Lepidopteran species may not host a resident microbial community, but rather a transient one, acquired from their environment and diet. Studies directly testing these hypotheses are however scarce and come from an even more limited number of species. By coupling comparative metabarcoding, immune gene expression, and metabolomics analyses with experimental manipulation of the gut microbial community of prediapause larvae of the Glanville fritillary butterfly (Melitaea cinxia, L.), we tested whether the gut microbial community supports early larval growth and survival, or modulates metabolism or immunity during early stages of development. We successfully altered this microbiota through antibiotic treatments and consecutively restored it through fecal transplants from conspecifics. Our study suggests that although the microbiota is involved in the up-regulation of an antimicrobial peptide, it did not affect the life history traits or the metabolism of early instars larvae. This study confirms the poor impact of the microbiota on diverse life history traits of yet another Lepidoptera species. However, it also suggests that potential eco-evolutionary host-symbiont strategies that take place in the gut of herbivorous butterfly hosts might have been disregarded, particularly how the microbiota may affect the host immune system homeostasis.</p>}},
author = {{Duplouy, Anne and Minard, Guillaume and Saastamoinen, Marjo}},
issn = {{2045-7758}},
keywords = {{antibiotic treatment; gut microbial community; immunity; larval development; larval survival; metabolites}},
language = {{eng}},
number = {{16}},
pages = {{8755--8769}},
publisher = {{Wiley-Blackwell}},
series = {{Ecology and Evolution}},
title = {{The gut bacterial community affects immunity but not metabolism in a specialist herbivorous butterfly}},
url = {{http://dx.doi.org/10.1002/ece3.6573}},
doi = {{10.1002/ece3.6573}},
volume = {{10}},
year = {{2020}},
}