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High-sensitivity detection of Mycobacterium tuberculosis DNA in tongue swab samples.
Olson, Alaina M; Wood, Rachel C; Weigel, Kris M; Yan, Alexander J; Lochner, Katherine A; Dragovich, Rane B; Luabeya, Angelique K; Yager, Paul; Hatherill, Mark; Cangelosi, Gerard A.
Afiliación
  • Olson AM; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
  • Wood RC; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
  • Weigel KM; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
  • Yan AJ; Department of Bioengineering, University of Washington, Seattle, Washington, United States of America.
  • Lochner KA; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
  • Dragovich RB; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
  • Luabeya AK; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease & Molecular Medicine and Department of Pathology, Faculty of Health Sciences, University of Cape Town, South Africa.
  • Yager P; Department of Bioengineering, University of Washington, Seattle, Washington, United States of America.
  • Hatherill M; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease & Molecular Medicine and Department of Pathology, Faculty of Health Sciences, University of Cape Town, South Africa.
  • Cangelosi GA; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
medRxiv ; 2024 Jul 27.
Article en En | MEDLINE | ID: mdl-39108520
ABSTRACT
Tongue swab (TS) sampling combined with qPCR to detect Mycobacterium tuberculosis (MTB) DNA is a promising alternative to sputum testing for tuberculosis (TB) diagnosis. In prior studies, the sensitivity of tongue swabbing has usually been lower than sputum. In this study, we evaluated two strategies to improve sensitivity. In one, centrifugation was used to concentrate tongue dorsum bacteria from 2-mL suspensions eluted from high-capacity foam swab samples. The pellets were resuspended as 500-µL suspensions, and then mechanically lysed prior to dual-target qPCR to detect MTB insertion elements IS6110 and IS1081. Fractionation experiments demonstrated that most of the MTB DNA signal in clinical swab samples (99.22% ± 1.46%) was present in the sedimentable fraction. When applied to archived foam swabs collected from 124 South Africans with presumptive TB, this strategy exhibited 83% sensitivity (71/86) and 100% specificity (38/38) relative to sputum MRS (microbiological reference standard; sputum culture and/or Xpert® Ultra). The second strategy used sequence-specific magnetic capture (SSMaC) to concentrate DNA released from MTB cells. This protocol was evaluated on archived Copan FLOQSwabs® flocked swab samples collected from 128 South African participants with presumptive TB. Material eluted into 500 µL buffer was mechanically lysed. The suspensions were digested by proteinase K, hybridized to biotinylated dual-target oligonucleotide probes, and then concentrated ~20-fold using magnetic separation. Upon dual-target qPCR testing of concentrates, this strategy exhibited 90% sensitivity (83/92) and 97% specificity (35/36) relative to sputum MRS. These results point the way toward automatable, high-sensitivity methods for detecting MTB DNA in TS. Importance Improved testing for tuberculosis (TB) is needed. Using a more accessible sample type than sputum may enable the detection of more cases, but it is critical that alternative samples be tested appropriately. Here, we describe two new, highly accurate methods for testing tongue swabs for TB DNA.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: MedRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: MedRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos