Evidence map›Paper›PMID 41525034›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Development and evaluation of 'Quick TB DNA Extraction' kit for the rapid and efficient detection of multidrug-resistant tuberculosis from sputum transported on bio-safe filter.

Rakesh Kumar Gupta, Keerti Chauhan, Ritu Singhal, Divya Anthwal, Vithal Prasad Myneedu, Khalid Umar Khayyam, Sangeeta Choudhary, Ashawant Gupta, Nalini Kant Gupta, Manjula Singh and 3 more

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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5 · Who and what money

Authors and funding

13 authors.

Rakesh Kumar Gupta *Department of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Keerti Chauhan *Department of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Ritu SinghalDepartment of Microbiology, National Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.
Divya AnthwalDepartment of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Vithal Prasad MyneeduDepartment of Microbiology, National Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.
Khalid Umar KhayyamDepartment of Microbiology, National Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.
Sangeeta ChoudharyDepartment of Bioscience and Biotechnology, Banasthali Vidyapith, P.O. Banasthali Vidyapith, Rajasthan, 304022, India.
Ashawant GuptaAdvanced Microdevices Pvt Ltd, Industrial Area, Ambala Cantt, India.
Nalini Kant GuptaAdvanced Microdevices Pvt Ltd, Industrial Area, Ambala Cantt, India.
Manjula SinghIndia Tuberculosis Research Consortium (ITRC), Indian Council of Medical Research, V. Ramalingaswami Bhawan, Ansari Nagar, New Delhi, India.
Jaya Sivaswami TyagiDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Manpreet BhallaDepartment of Microbiology, National Institute of Tuberculosis and Respiratory Diseases, New Delhi, India. mnprtbhalla@yahoo.com.
Sagarika HaldarDepartment of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India. sagarikahaldar.pgimer@gmail.com.ORCID http://orcid.org/0000-0001-8276-4458

Funding

Indian Council of Medical Research 5/8/5/7/Adhoc/2020/ECD-I
6 · The paper itself

Abstract

purposeWe recently demonstrated the utility of the 'TB Concentration & Transport' kit for bio-safe, ambient-temperature transport of dried sputum samples on Trans-Filter, along with the 'TB DNA Extraction' kit for efficient DNA extraction from Trans-Filter for use in the Line Probe Assay (LPA) for diagnosing drug-resistant tuberculosis (TB). The present study aimed to develop and evaluate a new 'Quick TB DNA Extraction' kit ('Quick DNA' kit) for rapid DNA isolation from Trans-Filter samples and assess its compatibility with LPA for the detection of multidrug-resistant TB (MDR-TB).

methodsConsecutive presumptive TB/MDR-TB/XDR-TB patients (n = 1823) were screened using LED-FM and/or TBDetect microscopy at 2 Designated Microscopy Centres associated with the National Institute of Tuberculosis and Respiratory Diseases (NITRD), New Delhi. Smear-positive samples (n = 235) were processed in duplicate using the 'TB Concentration and Transport' kit. Dried sputum on bio-safe Trans-Filters was transported at ambient temperature, along with sputum samples, in a 3-layer packing in cooling conditions to NITRD Hospital (a National Reference Laboratory). DNA was extracted from Trans-Filters using 'Quick DNA' kit and the 'TB DNA Extraction' kit, and from sputum using Hain's GenoLyse® DNA Extraction kit for first-line LPA for MDR-TB detection.

resultsQuick Kit-LPA and Kit-LPA (LPA with DNA extracted from Trans-Filter using 'Quick DNA' kit and 'TB DNA Extraction' kit, respectively) showed similar sensitivity of 88.9% (95% CI: 65.3-98.6) and 88.5% (95% CI: 69.9-97.5) and specificity of 100% (95% CI: 98.2-100) and 99.5% (95% CI: 97.3-99.9) for rifampicin and isoniazid resistance detection, respectively against Direct-LPA (LPA with DNA extracted from sputum samples using GenoLyse kit). User feedback obtained from laboratory technicians corroborated that the one-step 'Quick DNA' kit procedure was rapid (5 minutes), easy to perform, seamlessly integrated with LPA testing, and was suitable as a replacement for Kit-LPA or Direct-LPA. - ,

conclusionThe gap between drug-resistant TB detection and treatment initiation can be narrowed through Universal-Drug Susceptibility Testing by implementing (i) bio-safe and ambient temperature transport of sputum from primary healthcare centres to central laboratories, and (ii) by using Quick Kit-LPA over Direct-LPA in patients residing in remote areas.

Indexed as

Molecular Diagnostic TechniquesMycobacterium tuberculosisReagent Kits, DiagnosticSpecimen HandlingTuberculosis, Multidrug-ResistantAntitubercular AgentsDNA, BacterialFiltrationHumansSensitivity and SpecificitySputumAntitubercular AgentsDNA, BacterialReagent Kits, DiagnosticDrug-resistanceFilter-membraneLPASputumTransportTuberculosis

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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.