In vitro activity of rifampicin and verapamil combination in multidrug-resistant mycobacterium tuberculosis.
Fernanda de Oliveira Demitto, Renata Claro Ribeiro do Amaral, Flaviane Granero Maltempe, Vera Lúcia Dias Siqueira, Regiane Bertin de Lima Scodro, Mariana Aparecida Lopes, Katiany R Caleffi-Ferracioli, Pedro Henrique Canezin, Rosilene Fressatti Cardoso
Author Information
Fernanda de Oliveira Demitto: Postgraduation in Health Sciences, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Renata Claro Ribeiro do Amaral: Postgraduation in Bioscience and Pathophysiology, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Flaviane Granero Maltempe: Postgraduation in Bioscience and Pathophysiology, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Vera Lúcia Dias Siqueira: Laboratory of Medical Bacteriology, Department of Clinical Analysis and Biomedicine, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Regiane Bertin de Lima Scodro: Laboratory of Medical Bacteriology, Department of Clinical Analysis and Biomedicine, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Mariana Aparecida Lopes: Postgraduation in Bioscience and Pathophysiology, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Katiany R Caleffi-Ferracioli: Laboratory of Medical Bacteriology, Department of Clinical Analysis and Biomedicine, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Pedro Henrique Canezin: Postgraduation in Health Sciences, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
Rosilene Fressatti Cardoso: Laboratory of Medical Bacteriology, Department of Clinical Analysis and Biomedicine, State University of Maringa, Avenida Colombo, 5790, Maringa, Parana, 87020-900, Brazil.
The aim of the present study was to evaluate the effect of the combination of rifampicin (RIF) and verapamil (VP) against the Mycobacterium tuberculosis H37Rv reference strain and six multidrug-resistant (MDR) M. tuberculosis clinical isolates by determining Time-Kill Curves and the ability to efflux drug by fluorometry. The RIF+VP combination showed synergism in one MDR clinical isolate. For the other five MDR clinical isolates, the drug combination showed no interaction. The MDR clinical isolate had lower ethidium bromide (EtBr) accumulation when exposed to the RIF+VP combination, compared with RIF and VP exposure alone. The other MDR clinical isolates showed no significant difference in EtBr accumulation. These results suggest greater efflux action in one of the MDR clinical isolates compared with the M. tuberculosis H37Rv reference strain. The other five MDR isolates may have additional mechanisms of drug resistance to RIF. The use of the RIF+VP combination made one MDR bacillus more susceptible to RIF probably by inhibiting efflux pumps, and this combination therapy, in some cases, may contribute to a reduction of resistance to RIF in M. tuberculosis.
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