Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif

<p>Microbiome analysis has relied largely on metagenomics to characterize microbial populations and predict their functions. Here, we used a metaproteomic analysis of the fecal microbiome in piglets before and after weaning to compare protein abundances as they pertain to microbial populations...

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Main Author: Israel Rivera (3471599) (author)
Other Authors: KaLynn Harlow (5236988) (author), Robert N. Cole (82811) (author), Robert O’Meally (789845) (author), Wesley Garrett (1397437) (author), Weili Xiong (1348971) (author), William Oliver (5337962) (author), James E. Wells (11257785) (author), Katie Lynn Summers (7473512) (author), Nisan Chhetri (21236264) (author), Olga Postnikova (6998345) (author), Lea Rempel (21236267) (author), Matt Crouse (21236270) (author), Bryan Neville (21236273) (author), Cary Pirone Davies (14261792) (author)
Published: 2025
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_version_ 1852020832035930112
author Israel Rivera (3471599)
author2 KaLynn Harlow (5236988)
Robert N. Cole (82811)
Robert O’Meally (789845)
Wesley Garrett (1397437)
Weili Xiong (1348971)
William Oliver (5337962)
James E. Wells (11257785)
Katie Lynn Summers (7473512)
Nisan Chhetri (21236264)
Olga Postnikova (6998345)
Lea Rempel (21236267)
Matt Crouse (21236270)
Bryan Neville (21236273)
Cary Pirone Davies (14261792)
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Israel Rivera (3471599)
KaLynn Harlow (5236988)
Robert N. Cole (82811)
Robert O’Meally (789845)
Wesley Garrett (1397437)
Weili Xiong (1348971)
William Oliver (5337962)
James E. Wells (11257785)
Katie Lynn Summers (7473512)
Nisan Chhetri (21236264)
Olga Postnikova (6998345)
Lea Rempel (21236267)
Matt Crouse (21236270)
Bryan Neville (21236273)
Cary Pirone Davies (14261792)
author_role author
dc.creator.none.fl_str_mv Israel Rivera (3471599)
KaLynn Harlow (5236988)
Robert N. Cole (82811)
Robert O’Meally (789845)
Wesley Garrett (1397437)
Weili Xiong (1348971)
William Oliver (5337962)
James E. Wells (11257785)
Katie Lynn Summers (7473512)
Nisan Chhetri (21236264)
Olga Postnikova (6998345)
Lea Rempel (21236267)
Matt Crouse (21236270)
Bryan Neville (21236273)
Cary Pirone Davies (14261792)
dc.date.none.fl_str_mv 2025-05-02T10:52:05Z
dc.identifier.none.fl_str_mv 10.3389/fmicb.2025.1504433.s005
dc.relation.none.fl_str_mv https://figshare.com/articles/figure/Image_2_A_metaproteomic_analysis_of_the_piglet_fecal_microbiome_across_the_weaning_transition_tif/28919900
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Microbiology
metaproteome
microbiome
weaning
digestion
swine
dc.title.none.fl_str_mv Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
dc.type.none.fl_str_mv Image
Figure
info:eu-repo/semantics/publishedVersion
image
description <p>Microbiome analysis has relied largely on metagenomics to characterize microbial populations and predict their functions. Here, we used a metaproteomic analysis of the fecal microbiome in piglets before and after weaning to compare protein abundances as they pertain to microbial populations specific to either a milk- or plant-based diet. Fecal samples were collected from six piglets on the day of weaning and 4 weeks after transitioning to a standard nursery diet. Using the 12,554 protein groups identified in samples, we confirmed the shift in protein composition that takes place in response to the microbial succession following weaning and demonstrated the redundancy in metabolic processes between taxa. We identified taxa with roles as primary degraders based on corresponding proteins synthesized, thereby providing evidence for cross-feeding. Proteins associated with the breakdown of milk-specific carbohydrates were common among pre-weaned pigs, whereas the proteome of post-weaned piglets contained a greater abundance of proteins involved in the breaking down plant-specific carbohydrates. Furthermore, output revealed that production of propionate takes place via the propionaldehyde pathway in pre-weaned piglets, but changes to production via the succinate pathway in post-weaned piglets. Finally, a disproportionate quantity of carbohydrate-active enzymes (CAZymes) (~8%) were produced by fungi, which typically only represent ~0.1% of the microbiome taxa. Information gathered through this characterization of the metaproteome before and after weaning revealed important differences regarding the role of members in the microbial community, thereby providing information for the optimization of diets and products for both piglet and microbiome health.</p>
eu_rights_str_mv openAccess
id Manara_7b025e34646e07794fe8d8d80aa439dd
identifier_str_mv 10.3389/fmicb.2025.1504433.s005
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/28919900
publishDate 2025
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rights_invalid_str_mv CC BY 4.0
spelling Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tifIsrael Rivera (3471599)KaLynn Harlow (5236988)Robert N. Cole (82811)Robert O’Meally (789845)Wesley Garrett (1397437)Weili Xiong (1348971)William Oliver (5337962)James E. Wells (11257785)Katie Lynn Summers (7473512)Nisan Chhetri (21236264)Olga Postnikova (6998345)Lea Rempel (21236267)Matt Crouse (21236270)Bryan Neville (21236273)Cary Pirone Davies (14261792)Microbiologymetaproteomemicrobiomeweaningdigestionswine<p>Microbiome analysis has relied largely on metagenomics to characterize microbial populations and predict their functions. Here, we used a metaproteomic analysis of the fecal microbiome in piglets before and after weaning to compare protein abundances as they pertain to microbial populations specific to either a milk- or plant-based diet. Fecal samples were collected from six piglets on the day of weaning and 4 weeks after transitioning to a standard nursery diet. Using the 12,554 protein groups identified in samples, we confirmed the shift in protein composition that takes place in response to the microbial succession following weaning and demonstrated the redundancy in metabolic processes between taxa. We identified taxa with roles as primary degraders based on corresponding proteins synthesized, thereby providing evidence for cross-feeding. Proteins associated with the breakdown of milk-specific carbohydrates were common among pre-weaned pigs, whereas the proteome of post-weaned piglets contained a greater abundance of proteins involved in the breaking down plant-specific carbohydrates. Furthermore, output revealed that production of propionate takes place via the propionaldehyde pathway in pre-weaned piglets, but changes to production via the succinate pathway in post-weaned piglets. Finally, a disproportionate quantity of carbohydrate-active enzymes (CAZymes) (~8%) were produced by fungi, which typically only represent ~0.1% of the microbiome taxa. Information gathered through this characterization of the metaproteome before and after weaning revealed important differences regarding the role of members in the microbial community, thereby providing information for the optimization of diets and products for both piglet and microbiome health.</p>2025-05-02T10:52:05ZImageFigureinfo:eu-repo/semantics/publishedVersionimage10.3389/fmicb.2025.1504433.s005https://figshare.com/articles/figure/Image_2_A_metaproteomic_analysis_of_the_piglet_fecal_microbiome_across_the_weaning_transition_tif/28919900CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/289199002025-05-02T10:52:05Z
spellingShingle Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
Israel Rivera (3471599)
Microbiology
metaproteome
microbiome
weaning
digestion
swine
status_str publishedVersion
title Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
title_full Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
title_fullStr Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
title_full_unstemmed Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
title_short Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
title_sort Image 2_A metaproteomic analysis of the piglet fecal microbiome across the weaning transition.tif
topic Microbiology
metaproteome
microbiome
weaning
digestion
swine