Rapid Detection of Mycobacterium tuberculosis in Pleural Fluid Using Resuscitation-Promoting Factor-Based Thin Layer Agar Culture Method

Pleural tuberculous is difficult to diagnose. Culture is still considered the gold standard, especially in resource-limited settings where quick, cheap, and easy techniques are needed. The aim of the study was to evaluate resuscitation-promoting factors (Rpfs)-based thin layer agar (TLA) culture met...

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Published inFrontiers in microbiology Vol. 13; p. 803521
Main Authors Du, Fengjiao, Xing, Aiying, Li, Zihui, Pan, Liping, Jia, Hongyan, Du, Boping, Sun, Qi, Wei, Rongrong, Liu, Zhongquan, Zhang, Zongde
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 16.02.2022
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Summary:Pleural tuberculous is difficult to diagnose. Culture is still considered the gold standard, especially in resource-limited settings where quick, cheap, and easy techniques are needed. The aim of the study was to evaluate resuscitation-promoting factors (Rpfs)-based thin layer agar (TLA) culture method for quick detection of in pleural fluid. Patients with suspected pleural TB were enrolled prospectively in our hospital, pleural fluid of all patients were collected, stained with Ziehl-Neelsen for acid-fast bacilli (AFB), cultured on Rpfs-TLA, TLA, and Löwenstein-Jensen (LJ) medium, and identified according to recommended procedures. A total of 137 suspected pleural TB were enrolled and categorized, including 103 pleural TB (49 confirmed and 54 probable pleural TB) and 34 non-TBP patients. The sensitivity of Rpfs-TLA for total pleural TB was 43.7% (34.5∼53.3%), higher than that of TLA 29.1% (21.2∼38.5%) and LJ 26.2% (18.7∼35.5%) ( 0.01), and all specificity was 100% in the diagnosis of pleural TB. Median time to detection of a positive culture was 11.8 days (95% CI 10.4∼13.4) for Rpfs-TLA, 21.0 days (95% CI 19.1∼22.9) for TLA, and 30.5 days (95% CI 28.5∼32.5) for LJ ( < 0.001). Rpfs-TLA is an accurate, rapid, cheap, and easy culture method, which makes it promising for use in clinical laboratories.
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Reviewed by: Vignesh Ramachandran, University of Kuala Lumpur, Malaysia; Evgeniya V. Nazarova, Immunology Discovery, Genentech, United States
These authors jointly supervised this work
These authors have contributed equally to this work
Edited by: Ales Lapanje, Institut Jožef Stefan (IJS), Slovenia
This article was submitted to Infectious Agents and Disease, a section of the journal Frontiers in Microbiology
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2022.803521