Evidence map›Paper›PMID 36447140›Full record

ArticleBMC microbiology2022

Airway microecology in rifampicin-resistant and rifampicin-sensitive pulmonary tuberculosis patients.

Xingshan Cai, Yang Luo, Yuanliang Zhang, Yuan Lin, Bitong Wu, Zhizhong Cao, Zuqiong Hu, Xingyi Wu, Shouyong Tan

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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  7. Bibliometric analysis of intestinal microbiota and lung diseases.Frontiers in cellular and infection microbiology · 2024
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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

9 authors at 1 institution in 1 country.

Xingshan Cai *Department of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Yang Luo *Department of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Yuanliang ZhangDepartment of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Yuan LinDepartment of Tuberculosis Internal Medicine, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Bitong WuDepartment of Tuberculosis Internal Medicine, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Zhizhong CaoDepartment of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Zuqiong HuDepartment of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Xingyi WuDepartment of Medical Laboratory, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China.
Shouyong TanDepartment of Tuberculosis Internal Medicine, Guangzhou Chest Hospital, Guangzhou, 510095, P. R. China. tanshouyong2021@163.com.
Guangzhou Chest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary tuberculosis is a chronic infectious disease of the respiratory system. It is still one of the leading causes of death from a single infectious disease, but it has been stuck in the study of a single pathogen. Recent studies have shown that many diseases are associated with disruption of the native microbiota. In this study we investigated the occurrence of tuberculosis and the correlation between drug resistance and respiratory flora. High-throughput 16 S rRNA gene sequencing was used to characterize the respiratory microbiota composition of 30 tuberculosis (TB) affected patients and compared with 30 healthy (H) controls. According to their Gene Xpert results, 30 pulmonary tuberculosis patients were divided into 12 persons in the drug-sensitive group (DS0) and 18 persons in the drug-resistant group (DR0). The microbial flora of the two were compared with the H group.

resultsThe data generated by sequencing showed that Firmicutes, Proteus, Bacteroides, Actinomyces and Fusobacterium were the five main bacterial phyla detected, and they constituted more than 96% of the microbial community. The relative abundances of Fusobacterium, Haemophilus, Porphyromonas, Neisseria, TM7, Spirochetes, SR1, and Tenericutes in the TB group was lower than that of the H group, and Granulicatella was higher than the H group. The PcoA diagrams of the two groups had obvious clustering differences. The Alpha diversity of the TB group was lower than that of the H group, and the Beta diversity was higher than that of the H group (P < 0.05). The relative abundance of Streptococcus in the DS0 group was significantly higher than that in the DR0 group (P < 0.05).

conclusionPulmonary tuberculosis can cause disorders of the respiratory tract microbial flora, in which the relative abundance of Streptococcus was significantly different between rifampicin-sensitive and rifampicin-resistant patients.

Indexed as

MicrobiotaTuberculosis, PulmonaryFusobacteriumHumansRespiratory SystemRifampinRifampin16S rRNA gene sequencingMicrobial floraTuberculosis

Identifiers

PMID36447140
PMCPMC9706898
OpenAlexW4310363050

What OpenQuestion holds

Textmetadata
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.