Evidence map›Paper›PMID 35314755›Full record

ArticleScientific reports2022

Dynamic alterations in the lung microbiota in a rat model of lipopolysaccharide-induced acute lung injury.

Zhigang Tian, Enqi Wu, Jia You, Gang Ma, Shenzhen Jiang, Yuanyuan Liu, Jia Hou, Sihan Hou, Yaqin Ling, Lingpeng Pei and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Acute Endotoxemia-Induced Respiratory and Intestinal Dysbiosis.International journal of molecular sciences · 2022
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Zhigang TianDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China.
Enqi WuKey Laboratory of Ethnomedicine (Minzu University of China), Ministry of Education, Minzu University of China, No. 27 Zhongguancun South Avenue, Beijing, 100081, China. 2012006@muc.edu.cn.
Jia YouBiotherapy Center, The Seventh Medical Center of PLA General Hospital, Beijing, China.
Gang MaDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China.
Shenzhen JiangDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China.
Yuanyuan LiuDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China.
Jia HouDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China.
Sihan HouKey Laboratory of Ethnomedicine (Minzu University of China), Ministry of Education, Minzu University of China, No. 27 Zhongguancun South Avenue, Beijing, 100081, China.
Yaqin LingKey Laboratory of Ethnomedicine (Minzu University of China), Ministry of Education, Minzu University of China, No. 27 Zhongguancun South Avenue, Beijing, 100081, China.
Lingpeng PeiKey Laboratory of Ethnomedicine (Minzu University of China), Ministry of Education, Minzu University of China, No. 27 Zhongguancun South Avenue, Beijing, 100081, China.
Xiwei ZhengDepartment of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, No. 804 Shenglijie, Xingqing District, Yinchuan, 750004, China. zhengxiwei1964@163.com.
Ningxia Medical University · CNMinzu University of China · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lung microbiota have been found to be substantially altered in numerous pulmonary disorders, and crosstalk between the host pathophysiology and lung microbiota plays critical roles in the regulation of disease states. The aim of this study was to investigate dynamic changes in the lung microbiota during different stages of acute lung injury and acute respiratory distress syndrome (ALI/ARDS). Rats receiving an intraperitoneal administration of lipopolysaccharide (LPS) were sacrificed at 12 and 48 h after injection, and the hematological parameters, serum cytokine levels, and histological characteristics of the lung tissue and lung microbiota were assessed. After LPS injection, along with fluctuations of systemic cytokine levels and the onset and regression of pulmonary edema, the diversity, components, and functionalities of the pulmonary microbiota underwent significant dynamic changes. The volatility of the α-diversity indices narrowed after LPS injection, and the indices significantly decreased 48 h later. The abundance of 18 genera and functionality of adenosine triphosphate-binding cassette (ABC) transporters, pentose phosphate, and bacterial chemotaxis pathways were found to significantly differ between specified time points. Several significant correlations between the components and functionalities of the lung microbiota and indicative symptoms of ALI/ARDS were also observed. Brevibacterium was correlated with cytokines tumor necrosis factor (TNF)-α, interleukin (IL)-10, and IL-6 and with hematological percentage of neutrophils (NEU%); Wnt, Notch, and chronic myeloid leukemia signaling pathways were correlated with IL-1β; mitogen-activated protein kinase (MAPK) signaling pathway-yeast was correlated with IL-10; and the pathways of ascorbate and aldarate metabolism and basal transcription factors were correlated with platelet-related indicators. The correlations between the lung microbiota and indicative symptoms of ALI/ARDS identified in this study support further investigation into the underlying mechanism of host-microbiota interactions during lung injury and repair.

Indexed as

Acute Lung InjuryMicrobiotaRespiratory Distress SyndromeAnimalsCytokinesLipopolysaccharidesLungRatsTumor Necrosis Factor-alphaCytokinesLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID35314755
PMCPMC8938502
OpenAlexW4220718171

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.