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The chemotherapeutic drug methotrexate selects for antibiotic resistance

Gudmundsdottir, Jonina S. (author)
UiT Arctic Univ Norway, Fac Hlth Sci, Dept Pharm, Sykehusveien 44, N-9019 Tromso, Norway
Fredheim, Elizabeth G. A. (author)
UiT Arctic Univ Norway, Fac Hlth Sci, Dept Pharm, Sykehusveien 44, N-9019 Tromso, Norway
Koumans, Catharina I. M. (author)
Leiden Univ, Inst Biol, Leiden, Netherlands
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Hegstad, Joachim (author)
UiT Arctic Univ Norway, Fac Hlth Sci, Dept Pharm, Sykehusveien 44, N-9019 Tromso, Norway.;Univ Hosp North Norway, Dept Microbiol & Infect Control, Res & Dev Div, Tromso, Norway
Tang, Po-Cheng (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Andersson, Dan I. (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Samuelsen, Ørjan (author)
UiT Arctic Univ Norway, Fac Hlth Sci, Dept Pharm, Sykehusveien 44, N-9019 Tromso, Norway.;Univ Hosp North Norway, Norwegian Natl Advisory Unit Detect Antimicrobial, Dept Microbiol & Infect Control, Tromso, Norway
Johnsen, Pål J. (author)
UiT Arctic Univ Norway, Fac Hlth Sci, Dept Pharm, Sykehusveien 44, N-9019 Tromso, Norway
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 (creator_code:org_t)
Elsevier, 2021
2021
English.
In: EBioMedicine. - : Elsevier. - 2352-3964. ; 74
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Understanding drivers of antibiotic resistance evolution is fundamental for designing optimal treatment strategies and interventions to reduce the spread of antibiotic resistance. Various cytotoxic drugs used in cancer chemotherapy have antibacterial properties, but how bacterial populations are affected by these selective pressures is unknown. Here we test the hypothesis that the widely used cytotoxic drug methotrexate affects the evolution and selection of antibiotic resistance.Methods: First, we determined methotrexate susceptibility (IC90) and selective abilities in a collection of Escherichia coli and Klebsiella pneumoniae strains with and without pre-existing trimethoprim resistance determinants. We constructed fluorescently labelled pairs of E. coli MG1655 differing only in trimethoprim resistance determinants and determined the minimum selective concentrations of methotrexate using flow-cytometry. We further used an experimental evolution approach to investigate the effects of methotrexate on de novo trimethoprim resistance evolution.Findings: We show that methotrexate can select for acquired trimethoprim resistance determinants located on the chromosome or a plasmid. Additionally, methotrexate co-selects for genetically linked resistance determinants when present together with trimethoprim resistance on a multi-drug resistance plasmid. These selective effects occur at concentrations 40- to >320-fold below the methotrexate minimal inhibitory concentration.Interpretation: Our results strongly suggest a selective role of methotrexate for virtually any antibiotic resistance determinant when present together with trimethoprim resistance on a multi-drug resistance plasmid. The presented results may have significant implications for patient groups strongly depending on effective antibiotic treatment.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Läkemedelskemi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medicinal Chemistry (hsv//eng)

Keyword

Chemotherapeutic drugs
E. coli
Antibiotic resistance
Methotrexate
Resistance evolution

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