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Second-line drug susceptibility breakpoints for Mycobacterium tuberculosis using the MODS assay.
Trollip, A P; Moore, D; Coronel, J; Caviedes, L; Klages, S; Victor, T; Romancenco, E; Crudu, V; Ajbani, K; Vineet, V P; Rodrigues, C; Jackson, R L; Eisenach, K; Garfein, R S; Rodwell, T C; Desmond, E; Groessl, E J; Ganiats, T G; Catanzaro, A.
Affiliation
  • Trollip AP; Biomedical Sciences, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Medical Research Council Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa.
  • Moore D; TB Centre and Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK; Laboratorio de Investigación de Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
  • Coronel J; Laboratorio de Investigación de Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
  • Caviedes L; Laboratorio de Investigación de Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
  • Klages S; Biomedical Sciences, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Medical Research Council Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa.
  • Victor T; Biomedical Sciences, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Medical Research Council Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa.
  • Romancenco E; Microbiology and Morphology Laboratory, Phthisiopneumology Institute, Chisinau, Moldova.
  • Crudu V; Microbiology and Morphology Laboratory, Phthisiopneumology Institute, Chisinau, Moldova.
  • Ajbani K; Department of Microbiology, Parmanand Deepchand Hinduja National Hospital and Medical Research Centre Tertiary Care Hospital, Mumbai, India.
  • Vineet VP; Department of Microbiology, Parmanand Deepchand Hinduja National Hospital and Medical Research Centre Tertiary Care Hospital, Mumbai, India.
  • Rodrigues C; Department of Microbiology, Parmanand Deepchand Hinduja National Hospital and Medical Research Centre Tertiary Care Hospital, Mumbai, India.
  • Jackson RL; University of California San Diego School of Medicine, La Jolla, California, USA.
  • Eisenach K; Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Garfein RS; University of California San Diego School of Medicine, La Jolla, California, USA.
  • Rodwell TC; Division of Global Public Health, University of California San Diego School of Medicine, La Jolla, California, USA.
  • Desmond E; Mycobacteriology and Mycology Section, Microbial Diseases Laboratory, California Department of Public Health, Richmond, California, USA.
  • Groessl EJ; University of California San Diego, Veterans' Affairs San Diego Healthcare System, La Jolla, California, USA.
  • Ganiats TG; University of California San Diego Health Services Research Center, UCSD, La Jolla, California, USA.
  • Catanzaro A; University of California San Diego School of Medicine, La Jolla, California, USA.
Int J Tuberc Lung Dis ; 18(2): 227-32, 2014 Feb.
Article in En | MEDLINE | ID: mdl-24429318
ABSTRACT

OBJECTIVE:

To establish breakpoint concentrations for the fluoroquinolones (moxifloxacin [MFX] and ofloxacin [OFX]) and injectable second-line drugs (amikacin [AMK], kanamycin [KM] and capreomycin [CPM]) using the microscopic observation drug susceptibility (MODS) assay.

SETTING:

A multinational study conducted between February 2011 and August 2012 in Peru, India, Moldova and South Africa.

DESIGN:

In the first phase, breakpoints for the fluoroquinolones and injectable second-line drugs (n = 58) were determined. In the second phase, MODS second-line drug susceptibility testing (DST) as an indirect test was compared to MGIT™ DST (n = 89). In the third (n = 30) and fourth (n = 156) phases, we determined the reproducibility and concordance of MODS second-line DST directly from sputum.

RESULTS:

Breakpoints for MFX (0.5 µg/ml), OFX (1 µg/ml), AMK (2 µg/ml), KM (5 µg/ml) and CPM (2.5 µg/ml) were determined. In all phases, MODS results were highly concordant with MGIT DST. The few discrepancies suggest that the MODS breakpoint concentrations for some drugs may be too low.

CONCLUSION:

MODS second-line DST yielded comparable results to MGIT second-line DST, and is thus a promising alternative. Further studies are needed to confirm the accuracy of the drug breakpoints and the reliability of MODS second-line DST as a direct test.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Tuberculosis, Pulmonary / Microbial Sensitivity Tests / Tuberculosis, Multidrug-Resistant / Drug Resistance, Multiple, Bacterial / Microscopy / Mycobacterium tuberculosis / Antitubercular Agents Type of study: Clinical_trials / Prognostic_studies Limits: Humans Country/Region as subject: Africa / America do sul / Asia / Europa / Peru Language: En Journal: Int J Tuberc Lung Dis Year: 2014 Type: Article Affiliation country: South Africa

Full text: 1 Database: MEDLINE Main subject: Tuberculosis, Pulmonary / Microbial Sensitivity Tests / Tuberculosis, Multidrug-Resistant / Drug Resistance, Multiple, Bacterial / Microscopy / Mycobacterium tuberculosis / Antitubercular Agents Type of study: Clinical_trials / Prognostic_studies Limits: Humans Country/Region as subject: Africa / America do sul / Asia / Europa / Peru Language: En Journal: Int J Tuberc Lung Dis Year: 2014 Type: Article Affiliation country: South Africa