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Rifamycin antibiotics and the mechanisms of their failure.
Adams, Rebekah A; Leon, Gabrielle; Miller, Natalia M; Reyes, Saira P; Thantrong, Chantal H; Thokkadam, Alina M; Lemma, Annabel S; Sivaloganathan, Darshan M; Wan, Xuanqing; Brynildsen, Mark P.
Afiliação
  • Adams RA; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Leon G; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Miller NM; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Reyes SP; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Thantrong CH; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Thokkadam AM; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Lemma AS; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Sivaloganathan DM; Program in Quantitative and Computational Biology, Princeton University, Princeton, NJ, USA.
  • Wan X; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA.
  • Brynildsen MP; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, USA. mbrynild@princeton.edu.
J Antibiot (Tokyo) ; 74(11): 786-798, 2021 11.
Article em En | MEDLINE | ID: mdl-34400805
ABSTRACT
Rifamycins are a class of antibiotics that were first discovered in 1957 and are known for their use in treating tuberculosis (TB). Rifamycins exhibit bactericidal activity against many Gram-positive and Gram-negative bacteria by inhibiting RNA polymerase (RNAP); however, resistance is prevalent and the mechanisms range from primary target modification and antibiotic inactivation to cytoplasmic exclusion. Further, phenotypic resistance, in which only a subpopulation of bacteria grow in concentrations exceeding their minimum inhibitory concentration, and tolerance, which is characterized by reduced rates of bacterial cell death, have been identified as additional causes of rifamycin failure. Here we summarize current understanding and recent developments regarding this critical antibiotic class.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rifamicinas / Tuberculose / Antibióticos Antituberculose Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rifamicinas / Tuberculose / Antibióticos Antituberculose Idioma: En Ano de publicação: 2021 Tipo de documento: Article