The imbalance of pulmonary Th17/Treg cells in BALB/c suckling mice infected with respiratory syncytial virus-mediated intestinal immune damage and gut microbiota changes

Author:

Liu Jiling12ORCID,Huang Yixuan3,Liu Nian4,Qiu Huan5,Zhang Xiaoyan1,Liu Xiaojie1,He Maozhang1ORCID,Chen Mingwei3ORCID,Huang Shenghai16ORCID

Affiliation:

1. Department of Microbiology, The Key Laboratory of Microbiology and Parasitology of Anhui Province, The Key Laboratory of Zoonoses of High Institutions in Anhui, School of Basic Medical Sciences, Anhui Medical University, Hefei, Anhui, China

2. College of Life Science, Hebei University, Baoding, Hebei, China

3. Department of Endocrinology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

4. Department of Critical Care Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

5. School of Nursing, Anhui Medical University, Hefei, Anhui, China

6. School of Life Sciences, Anhui Medical University, Hefei, Anhui, China

Abstract

ABSTRACT The immune response induced by respiratory syncytial virus (RSV) infection is closely related to changes in the composition and function of gastrointestinal microorganisms. However, the specific mechanism remains unknown and the pulmonary-intestinal axis deserves further study. In this study, the mRNA levels of ROR-γt and Foxp3 in the lung and intestine increased first and then decreased. IL-17 and IL-22 reached the maximum on the third day after infection in the lung, and on the second day after infection in the small intestine and colon, respectively. RegⅢγ in intestinal tissue reached the maximum on the third day after RSV infection. Moreover, the genus enriched in the RSV group was Aggregatibacter , and Proteus was reduced. RSV infection not only causes Th17/Treg cell imbalance in the lungs of mice but also leads to the release of excessive IL-22 from the lungs through blood circulation which binds to IL-22 receptors on the intestinal surface, inducing RegⅢγ overexpression, impaired intestinal Th17/Treg development, and altered gut microbiota composition. Our research reveals a significant link between the pulmonary and intestinal axis after RSV infection. IMPORTANCE RSV is the most common pathogen causing acute lower respiratory tract infections in infants and young children, but the complex interactions between the immune system and gut microbiota induced by RSV infection still requires further research. In this study, it was suggested that RSV infection in 7-day-old BALB/c suckling mice caused lung inflammation and disruption of Th17/Treg cells development, and altered the composition of gut microbiota through IL-22 induced overexpression of RegⅢγ, leading to intestinal immune injury and disruption of gut microbiota. This research reveals that IL-22 may be the link between the lung and gut. This study may provide a new insight into the intestinal symptoms caused by RSV and other respiratory viruses and the connection between the lung and gut axis, as well as new therapeutic ideas for the treatment of RSV-infected children.

Funder

MOST | National Natural Science Foundation of China

the Natural National Science Foundation of China

Major Project of Natural Science Research of Anhui Education Department

Research Fund of Anhui Institute of Translational Medicine

National First-Class Undergraduate Program Construction Point

Projects of Education Quality Engineering of Anhui Province

Publisher

American Society for Microbiology

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