Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia

Abstract Background Mounting experimental evidence has shown that the gut microbiota plays a significant role in the pathogenesis of mastitis, and clinical investigations have found that the occurrence of mastitis is correlated with ruminal dysbiosis. However, the underlying mechanism by which the r...

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Main Authors: Caijun Zhao, Xiaoyu Hu, Lijuan Bao, Keyi Wu, Yihong Zhao, Kaihe Xiang, Shuang Li, Ying Wang, Min Qiu, Lianjun Feng, Xiangyue Meng, Naisheng Zhang, Yunhe Fu
Format: Article
Language:English
Published: BMC 2022-12-01
Series:Microbiome
Subjects:
Online Access:https://doi.org/10.1186/s40168-022-01402-z
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author Caijun Zhao
Xiaoyu Hu
Lijuan Bao
Keyi Wu
Yihong Zhao
Kaihe Xiang
Shuang Li
Ying Wang
Min Qiu
Lianjun Feng
Xiangyue Meng
Naisheng Zhang
Yunhe Fu
author_facet Caijun Zhao
Xiaoyu Hu
Lijuan Bao
Keyi Wu
Yihong Zhao
Kaihe Xiang
Shuang Li
Ying Wang
Min Qiu
Lianjun Feng
Xiangyue Meng
Naisheng Zhang
Yunhe Fu
author_sort Caijun Zhao
collection DOAJ
description Abstract Background Mounting experimental evidence has shown that the gut microbiota plays a significant role in the pathogenesis of mastitis, and clinical investigations have found that the occurrence of mastitis is correlated with ruminal dysbiosis. However, the underlying mechanism by which the ruminal microbiota participates in the development of mastitis remains unknown. Results In the present study, we found that cows with clinical mastitis had marked systemic inflammation, which was associated with significant ruminal dysbiosis, especially enriched Proteobacteria in the rumen. Ruminal microbiota transplantation from mastitis cows (M-RMT) to mice induced mastitis symptoms in recipient mice along with increased mammary proinflammatory signature activation of the TLR4-cGAS-STING-NF-κB/NLRP3 pathways. M-RMT also induced mucosal inflammation and impaired intestinal barrier integrity, leading to increased endotoxemia and systemic inflammation. Moreover, we showed that M-RMT mirrored ruminal microbiota disruption in the gut of recipient mice, as evidenced by enriched Proteobacteria and similar bacterial functions, which were correlated with most proinflammatory parameters and serum lipopolysaccharide (LPS) levels in mice. Recurrent low-grade LPS treatment mirrored gut dysbiosis-induced endotoxemia and caused severe mastitis in mice. Furthermore, we found that gut dysbiosis-derived LPS reduced host alkaline phosphatase activity by activating neuraminidase (Neu), which facilitates low-grade LPS exposure and E. coli-induced mastitis in mice. Conversely, treatment with calf intestinal alkaline phosphatase or the Neu inhibitor zanamivir alleviated low-grade LPS exposure and E. coli-induced mastitis in mice. Conclusions Our results suggest that ruminal dysbiosis-derived low-grade endotoxemia can cause mastitis and aggravate pathogen-induced mastitis by impairing host anti-inflammatory enzymes, which implies that regulating the ruminal or gut microbiota to prevent low-grade systemic inflammation is a potential strategy for mastitis intervention. Video Abstract
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spelling doaj.art-6bbe7ca475b84908ab46db7ffee9288a2022-12-22T03:48:25ZengBMCMicrobiome2049-26182022-12-0110112210.1186/s40168-022-01402-zGut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemiaCaijun Zhao0Xiaoyu Hu1Lijuan Bao2Keyi Wu3Yihong Zhao4Kaihe Xiang5Shuang Li6Ying Wang7Min Qiu8Lianjun Feng9Xiangyue Meng10Naisheng Zhang11Yunhe Fu12Department of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Breast Center, West China Hospital, Sichuan UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityDepartment of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin UniversityAbstract Background Mounting experimental evidence has shown that the gut microbiota plays a significant role in the pathogenesis of mastitis, and clinical investigations have found that the occurrence of mastitis is correlated with ruminal dysbiosis. However, the underlying mechanism by which the ruminal microbiota participates in the development of mastitis remains unknown. Results In the present study, we found that cows with clinical mastitis had marked systemic inflammation, which was associated with significant ruminal dysbiosis, especially enriched Proteobacteria in the rumen. Ruminal microbiota transplantation from mastitis cows (M-RMT) to mice induced mastitis symptoms in recipient mice along with increased mammary proinflammatory signature activation of the TLR4-cGAS-STING-NF-κB/NLRP3 pathways. M-RMT also induced mucosal inflammation and impaired intestinal barrier integrity, leading to increased endotoxemia and systemic inflammation. Moreover, we showed that M-RMT mirrored ruminal microbiota disruption in the gut of recipient mice, as evidenced by enriched Proteobacteria and similar bacterial functions, which were correlated with most proinflammatory parameters and serum lipopolysaccharide (LPS) levels in mice. Recurrent low-grade LPS treatment mirrored gut dysbiosis-induced endotoxemia and caused severe mastitis in mice. Furthermore, we found that gut dysbiosis-derived LPS reduced host alkaline phosphatase activity by activating neuraminidase (Neu), which facilitates low-grade LPS exposure and E. coli-induced mastitis in mice. Conversely, treatment with calf intestinal alkaline phosphatase or the Neu inhibitor zanamivir alleviated low-grade LPS exposure and E. coli-induced mastitis in mice. Conclusions Our results suggest that ruminal dysbiosis-derived low-grade endotoxemia can cause mastitis and aggravate pathogen-induced mastitis by impairing host anti-inflammatory enzymes, which implies that regulating the ruminal or gut microbiota to prevent low-grade systemic inflammation is a potential strategy for mastitis intervention. Video Abstracthttps://doi.org/10.1186/s40168-022-01402-zRuminal microbiotaMastitisDysbiosisLPSALPNeu
spellingShingle Caijun Zhao
Xiaoyu Hu
Lijuan Bao
Keyi Wu
Yihong Zhao
Kaihe Xiang
Shuang Li
Ying Wang
Min Qiu
Lianjun Feng
Xiangyue Meng
Naisheng Zhang
Yunhe Fu
Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
Microbiome
Ruminal microbiota
Mastitis
Dysbiosis
LPS
ALP
Neu
title Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
title_full Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
title_fullStr Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
title_full_unstemmed Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
title_short Gut dysbiosis induces the development of mastitis through a reduction in host anti-inflammatory enzyme activity by endotoxemia
title_sort gut dysbiosis induces the development of mastitis through a reduction in host anti inflammatory enzyme activity by endotoxemia
topic Ruminal microbiota
Mastitis
Dysbiosis
LPS
ALP
Neu
url https://doi.org/10.1186/s40168-022-01402-z
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