The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome

Abstract Animals living in high‐altitude environments, such as the Tibetan Plateau, must face harsh environmental conditions (e.g., hypoxia, cold, and strong UV radiation). These animals' physiological adaptations (e.g., increased red cell production and turnover rate) might also be associated...

Full description

Bibliographic Details
Main Authors: Dayong Li, Wancai Xia, Xinyuan Cui, Mei Zhao, Kai Huang, Xueyu Wang, Jian Shen, Hua Chen, Lifeng Zhu
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:Evolutionary Applications
Subjects:
Online Access:https://doi.org/10.1111/eva.13595
_version_ 1797541888262144000
author Dayong Li
Wancai Xia
Xinyuan Cui
Mei Zhao
Kai Huang
Xueyu Wang
Jian Shen
Hua Chen
Lifeng Zhu
author_facet Dayong Li
Wancai Xia
Xinyuan Cui
Mei Zhao
Kai Huang
Xueyu Wang
Jian Shen
Hua Chen
Lifeng Zhu
author_sort Dayong Li
collection DOAJ
description Abstract Animals living in high‐altitude environments, such as the Tibetan Plateau, must face harsh environmental conditions (e.g., hypoxia, cold, and strong UV radiation). These animals' physiological adaptations (e.g., increased red cell production and turnover rate) might also be associated with the gut microbial response. Bilirubin is a component of red blood cell turnover or destruction and is excreted into the intestine and reduced to urobilinoids and/or urobilinogen by gut bacteria. Here, we found that the feces of macaques living in high‐altitude regions look significantly browner (with a high concentration of stercobilin, a component from urobilinoids) than those living in low‐altitude regions. We also found that gut microbes involved in urobilinogen reduction (e.g., beta‐glucuronidase) were enriched in the high‐altitude mammal population compared to the low‐altitude population. Moreover, the spatial–temporal change in gut microbial function was more profound in the low‐altitude macaques than in the high‐altitude population, which might be attributed to profound changes in food resources in the low‐altitude regions. Therefore, we conclude that a high‐altitude environment's stress influences living animals and their symbiotic microbiota.
first_indexed 2024-03-10T13:23:02Z
format Article
id doaj.art-3775dae36ef543d98beef2b1dd70dba5
institution Directory Open Access Journal
issn 1752-4571
language English
last_indexed 2024-03-10T13:23:02Z
publishDate 2023-10-01
publisher Wiley
record_format Article
series Evolutionary Applications
spelling doaj.art-3775dae36ef543d98beef2b1dd70dba52023-11-21T09:52:38ZengWileyEvolutionary Applications1752-45712023-10-0116101708172010.1111/eva.13595The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiomeDayong Li0Wancai Xia1Xinyuan Cui2Mei Zhao3Kai Huang4Xueyu Wang5Jian Shen6Hua Chen7Lifeng Zhu8Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education) China West Normal University Nanchong ChinaKey Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education) China West Normal University Nanchong ChinaCollege of Life Science Nanjing Normal University Nanjing ChinaKey Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education) China West Normal University Nanchong ChinaKey Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education) China West Normal University Nanchong ChinaKey Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education) China West Normal University Nanchong ChinaHuadian Energy Co., Ltd. Tibet ChinaMingke Biotechnology Hangzhou ChinaSchool of Medicine & Holistic Integrative Medicine Nanjing University of Chinese Medicine Nanjing ChinaAbstract Animals living in high‐altitude environments, such as the Tibetan Plateau, must face harsh environmental conditions (e.g., hypoxia, cold, and strong UV radiation). These animals' physiological adaptations (e.g., increased red cell production and turnover rate) might also be associated with the gut microbial response. Bilirubin is a component of red blood cell turnover or destruction and is excreted into the intestine and reduced to urobilinoids and/or urobilinogen by gut bacteria. Here, we found that the feces of macaques living in high‐altitude regions look significantly browner (with a high concentration of stercobilin, a component from urobilinoids) than those living in low‐altitude regions. We also found that gut microbes involved in urobilinogen reduction (e.g., beta‐glucuronidase) were enriched in the high‐altitude mammal population compared to the low‐altitude population. Moreover, the spatial–temporal change in gut microbial function was more profound in the low‐altitude macaques than in the high‐altitude population, which might be attributed to profound changes in food resources in the low‐altitude regions. Therefore, we conclude that a high‐altitude environment's stress influences living animals and their symbiotic microbiota.https://doi.org/10.1111/eva.13595adaptationfecal colorgut microbiomehigh altitudeprimatesspatial–temporal changes
spellingShingle Dayong Li
Wancai Xia
Xinyuan Cui
Mei Zhao
Kai Huang
Xueyu Wang
Jian Shen
Hua Chen
Lifeng Zhu
The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
Evolutionary Applications
adaptation
fecal color
gut microbiome
high altitude
primates
spatial–temporal changes
title The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
title_full The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
title_fullStr The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
title_full_unstemmed The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
title_short The putatively high‐altitude adaptation of macaque monkeys: Evidence from the fecal metabolome and gut microbiome
title_sort putatively high altitude adaptation of macaque monkeys evidence from the fecal metabolome and gut microbiome
topic adaptation
fecal color
gut microbiome
high altitude
primates
spatial–temporal changes
url https://doi.org/10.1111/eva.13595
work_keys_str_mv AT dayongli theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT wancaixia theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT xinyuancui theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT meizhao theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT kaihuang theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT xueyuwang theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT jianshen theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT huachen theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT lifengzhu theputativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT dayongli putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT wancaixia putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT xinyuancui putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT meizhao putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT kaihuang putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT xueyuwang putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT jianshen putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT huachen putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome
AT lifengzhu putativelyhighaltitudeadaptationofmacaquemonkeysevidencefromthefecalmetabolomeandgutmicrobiome