Evidence map›Paper›PMID 41024077›Full record

ArticleAIDS research and therapy2025

Metagenomic next-generation sequencing for pathogen detection of pulmonary infections in persons living with HIV.

Yapeng Zhang, Shaowei Guo, Lihua Lu, Yimin Li, Yong Wu

Abstract read
In one paragraph

Article in AIDS research and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yapeng ZhangThe Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha, 410005, China.
Shaowei GuoHengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.
Lihua LuHengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.
Yimin LiThe Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha, 410005, China.
Yong WuThe Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha, 410005, China. wuyong_zn@csu.edu.cn.

Funding

Natural Science Foundation of Changsha kq2403197Natural Science Foundation of Hunan Province 2025JJ80470
6 · The paper itself

Abstract

backgroundThis study aimed to evaluate the diagnostic utility of metagenomic next-generation sequencing (mNGS) in detecting pulmonary infections in persons living with HIV(PLWH).

methodsWe conducted a retrospective study involving 246 PLWH with pulmonary infections. Bronchoalveolar lavage fluid (BALF) specimens were collected from all patients. mNGS and traditional microbial cultures were performed in parallel to compare the differences in pathogen identification. Patients were stratified by immune status based on CD4

resultsmNGS demonstrated a significantly higher pathogen detection sensitivity (98.0%) compared to traditional cultures (32.1%). The spectrum of pathogens detected by mNGS and culture methods differed significantly. mNGS identified 123 pathogenic microorganisms, whereas cultures detected only 17. mNGS detected additional pathogens, including viruses (e.g., Epstein-Barr virus and cytomegalovirus) and fastidious microorganisms (e.g., Pneumocystis jirovecii). Furthermore, mNGS revealed a significant correlation between PLWH-associated immunodeficiency and pathogen profiles. The diversity of pathogens, particularly fungi and viruses, increased with declining CD4

conclusionmNGS comprehensively characterizes the complex pathogen spectrum in PLWH-associated pulmonary infections, significantly enhancing detection sensitivity for mixed and fastidious infections, thereby guiding targeted anti-infective therapy. Immunosuppression severity strongly correlates with opportunistic pathogen profiles and the risk of specific pathogen detection, highlighting the importance of immune status-guided clinical strategies. mNGS serves as a valuable adjunct to conventional diagnostic methods, enhancing the detection and prognostic assessment of infectious complications in PLWH.

Indexed as

High-Throughput Nucleotide SequencingHIV InfectionsLung DiseasesMetagenomicsRespiratory Tract InfectionsAdultBronchoalveolar Lavage FluidCD4 Lymphocyte CountFemaleHumansMaleMiddle AgedRetrospective StudiesSensitivity and SpecificityAcquired immune deficiency syndromeMetagenomicsNext-generation sequencingPulmonary infection

Identifiers

PMID41024077
PMCPMC12481790

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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.