Evidence map›Paper›PMID 41691168›Full record

ArticleBMC infectious diseases2026

Acquired linezolid resistance in DR-TB: genotype-phenotype discordance and molecular heterogeneity in a retrospective cohort.

Wenqiang Zhou, Qingfeng Wang, Wenjuan Nie, Wenhui Shi, Yang Yang, Wenjie Qi, Yu Lu, Naihui Chu

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Wenqiang ZhouDepartment of Infectious Diseases, Beijing Friendship Hospital, Affiliated to Capital Medical University, No. 95, Yongan Road, Xicheng District, Beijing, 100050, China.
Qingfeng WangDepartment of Tuberculosis, Beijing Chest Hospital, Affiliated to Capital Medical University, No 9, Beiguan Street, Tongzhou District, Beijing, 101149, China.
Wenjuan NieDepartment of Tuberculosis, Beijing Chest Hospital, Affiliated to Capital Medical University, No 9, Beiguan Street, Tongzhou District, Beijing, 101149, China.
Wenhui ShiDepartment of Tuberculosis, Beijing Chest Hospital, Affiliated to Capital Medical University, No 9, Beiguan Street, Tongzhou District, Beijing, 101149, China.
Yang YangDepartment of Tuberculosis, Beijing Chest Hospital, Affiliated to Capital Medical University, No 9, Beiguan Street, Tongzhou District, Beijing, 101149, China.
Wenjie QiDepartment of Infectious Diseases, Beijing Friendship Hospital, Affiliated to Capital Medical University, No. 95, Yongan Road, Xicheng District, Beijing, 100050, China. qi_wenjie@ccmu.edu.cn.
Yu LuBeijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing Chest Hospital, Capital Medical University, Beijing, China. luyu4876@hotmail.com.
Naihui ChuDepartment of Tuberculosis, Beijing Chest Hospital, Affiliated to Capital Medical University, No 9, Beiguan Street, Tongzhou District, Beijing, 101149, China. chunaihui1994@sina.com.

Funding

Beijing Clinical Medicine Development Special Project "Sailing 3.0" ZLRK202331Beijing Municipal Health Commission Research Ward Excellent Clinical Research Program BRWEP2024W042160109Global Tuberculosis Drug Research and Development Alliance Cooperation Project of China Anti-TB Association CATA/TBA-20210310HQ7High-level Public Health Technology Talent Construction Project Academic Leader-02-29National Key Research and Development Program 2024YFC2311203Special Project of Guangzhou National Laboratory for 2024- Short Term Treatment of Tuberculosis GZNL2024A01030
6 · The paper itself

Abstract

backgroundLinezolid is an important drug for the treatment of drug-resistant tuberculosis (DR-TB). Acquired linezolid resistance threatens treatment efficacy. This study aimed to analyze the risk factors and molecular mechanisms of linezolid-acquired resistance in a clinical cohort.

methodsWe conducted a retrospective study of 61 patients with DR-TB who failed linezolid-containing regimens (2017–2021). Paired baseline and post-treatment Mycobacterium tuberculosis isolates were subjected to linezolid Minimum inhibitory concentration (MIC) testing (Microplate Alamar Blue Assay) and sequencing of rplC, rrl (23 S rRNA), and rplD. Acquired resistance was defined as a ≥ 4-fold increase in MIC or the presence of new resistance-conferring mutation. Risk factors were analyzed using logistic regression.

resultsAcquired linezolid resistance occurred in 31.1% (19/61) of patients. Younger age (< 37.5 years; OR = 1.04/year decrease, p = 0.012) and prolonged therapy (> 14.3 months; OR = 1.07/month, p = 0.004) were the independent risk factors. Sequencing revealed 26 mutation events across the longitudinal isolates; 57.7% (15/26) harbored rplC T460C (Cys154Arg), whereas 38.5% (10/26) had rrl mutations (G2270T, G2814T). A novel rplD A518T (Lys173Ile) mutation emerged concurrently with the rplC T460C mutation. Phenotypic-genotypic discordance occurred in 11.5% (3/26) of resistant isolates, including one strain with MIC elevation (0.25→4.0 mg/L) lacking target mutations. Linezolid resistance correlated with prior resistance to clofazimine (kappa = 0.538, p < 0.001), amikacin, and pasiniazid.

conclusionsYoung age, extended therapy, and ribosomal mutations drive linezolid resistance. Pretreatment susceptibility screening is critical.

Indexed as

Antitubercular AgentsDrug Resistance, BacterialLinezolidMycobacterium tuberculosisTuberculosis, Multidrug-ResistantAdultFemaleGenotypeHumansMaleMicrobial Sensitivity TestsMiddle AgedMutationPhenotypeRetrospective StudiesRibosomal ProteinsAntitubercular AgentsLinezolidRibosomal ProteinsRNA, Ribosomal, 23SAcquired drug resistanceLinezolid resistanceMycobacterium tuberculosisRibosomal mutationsRisk factors

Identifiers

PMID41691168
PMCPMC12980970

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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.