Sequential inactivation of rdxA (hp0954) and frxA (HP0642) nitroreductase genes causes moderate and high-level metronidazole resistance in Helicobacter pylori

J. Y. Jeong, A. K. Mukhopadhyay, D. Dailidiene, Y. Wang, B. Velapatino, Robert H Gilman, A. J. Parkinson, G. B. Nair, B. C Y Wong, Kum Lam Shiu Kum Lam, R. Mistry, I. Segal, Y. Yuan, H. Gao, T. Alarcon, M. L. Brea, Y. Ito, D. Kersulyte, H. K. Lee, Y. GongA. Goodwin, P. S. Hoffman, D. E. Berg

Research output: Contribution to journalArticle

Abstract

Helicobacter pylori is a human-pathogenic bacterial species that is subdivided geographically, with different genotypes predominating in different parts of the world. Here we test and extend an earlier conclusion that metronidazole (Mtz) resistance is due to mutation in rdxA (HP0954), which encodes a nitroreductase that converts Mtz from prodrug to bactericidal agent. We found that (i) rdxA genes PCR amplified from 50 representative Mtz(r) strains from previously unstudied populations in Asia, South Africa, Europe, and the Americas could, in each case, transform Mtz(s) H. pylori to Mtz(r); (ii) Mtz(r) mutant derivatives of a cultured Mtz(s) strain resulted from mutation in rdxA; and (iii) transformation of Mtz(s) strains with rdxA-null alleles usually resulted in moderate level Mtz resistance (16 μg/ml). However, resistance to higher Mtz levels was common among clinical isolates, a result that implicates at least one additional gene. Expression in Escherichia coli of frxA (HP0642; flavin oxidoreductase), an rdxA paralog, made this normally resistant species Mtz(s), and frxA inactivation enhanced Mtz resistance in rdxA-deficient cells but had little effect on the Mtz susceptibility of rdxA+ cells. Strains carrying frxA-null and rdxA-null alleles could mutate to even higher resistance, a result implicating one or more additional genes in residual Mtz susceptibility and hyperresistance. We conclude that most Mtz resistance in H. pylori depends on rdxA inactivation, that mutations in frxA can enhance resistance, and that genes that confer Mtz resistance without rdxA inactivation are rare or nonexistent in H. pylori populations.

Original languageEnglish (US)
Pages (from-to)5082-5090
Number of pages9
JournalJournal of Bacteriology
Volume182
Issue number18
DOIs
StatePublished - 2000
Externally publishedYes

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Nitroreductases
Metronidazole
Helicobacter pylori
Genes
Mutation
Alleles

ASJC Scopus subject areas

  • Applied Microbiology and Biotechnology
  • Immunology

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Sequential inactivation of rdxA (hp0954) and frxA (HP0642) nitroreductase genes causes moderate and high-level metronidazole resistance in Helicobacter pylori. / Jeong, J. Y.; Mukhopadhyay, A. K.; Dailidiene, D.; Wang, Y.; Velapatino, B.; Gilman, Robert H; Parkinson, A. J.; Nair, G. B.; Wong, B. C Y; Shiu Kum Lam, Kum Lam; Mistry, R.; Segal, I.; Yuan, Y.; Gao, H.; Alarcon, T.; Brea, M. L.; Ito, Y.; Kersulyte, D.; Lee, H. K.; Gong, Y.; Goodwin, A.; Hoffman, P. S.; Berg, D. E.

In: Journal of Bacteriology, Vol. 182, No. 18, 2000, p. 5082-5090.

Research output: Contribution to journalArticle

Jeong, JY, Mukhopadhyay, AK, Dailidiene, D, Wang, Y, Velapatino, B, Gilman, RH, Parkinson, AJ, Nair, GB, Wong, BCY, Shiu Kum Lam, KL, Mistry, R, Segal, I, Yuan, Y, Gao, H, Alarcon, T, Brea, ML, Ito, Y, Kersulyte, D, Lee, HK, Gong, Y, Goodwin, A, Hoffman, PS & Berg, DE 2000, 'Sequential inactivation of rdxA (hp0954) and frxA (HP0642) nitroreductase genes causes moderate and high-level metronidazole resistance in Helicobacter pylori', Journal of Bacteriology, vol. 182, no. 18, pp. 5082-5090. https://doi.org/10.1128/JB.182.18.5082-5090.2000
Jeong, J. Y. ; Mukhopadhyay, A. K. ; Dailidiene, D. ; Wang, Y. ; Velapatino, B. ; Gilman, Robert H ; Parkinson, A. J. ; Nair, G. B. ; Wong, B. C Y ; Shiu Kum Lam, Kum Lam ; Mistry, R. ; Segal, I. ; Yuan, Y. ; Gao, H. ; Alarcon, T. ; Brea, M. L. ; Ito, Y. ; Kersulyte, D. ; Lee, H. K. ; Gong, Y. ; Goodwin, A. ; Hoffman, P. S. ; Berg, D. E. / Sequential inactivation of rdxA (hp0954) and frxA (HP0642) nitroreductase genes causes moderate and high-level metronidazole resistance in Helicobacter pylori. In: Journal of Bacteriology. 2000 ; Vol. 182, No. 18. pp. 5082-5090.
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abstract = "Helicobacter pylori is a human-pathogenic bacterial species that is subdivided geographically, with different genotypes predominating in different parts of the world. Here we test and extend an earlier conclusion that metronidazole (Mtz) resistance is due to mutation in rdxA (HP0954), which encodes a nitroreductase that converts Mtz from prodrug to bactericidal agent. We found that (i) rdxA genes PCR amplified from 50 representative Mtz(r) strains from previously unstudied populations in Asia, South Africa, Europe, and the Americas could, in each case, transform Mtz(s) H. pylori to Mtz(r); (ii) Mtz(r) mutant derivatives of a cultured Mtz(s) strain resulted from mutation in rdxA; and (iii) transformation of Mtz(s) strains with rdxA-null alleles usually resulted in moderate level Mtz resistance (16 μg/ml). However, resistance to higher Mtz levels was common among clinical isolates, a result that implicates at least one additional gene. Expression in Escherichia coli of frxA (HP0642; flavin oxidoreductase), an rdxA paralog, made this normally resistant species Mtz(s), and frxA inactivation enhanced Mtz resistance in rdxA-deficient cells but had little effect on the Mtz susceptibility of rdxA+ cells. Strains carrying frxA-null and rdxA-null alleles could mutate to even higher resistance, a result implicating one or more additional genes in residual Mtz susceptibility and hyperresistance. We conclude that most Mtz resistance in H. pylori depends on rdxA inactivation, that mutations in frxA can enhance resistance, and that genes that confer Mtz resistance without rdxA inactivation are rare or nonexistent in H. pylori populations.",
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T1 - Sequential inactivation of rdxA (hp0954) and frxA (HP0642) nitroreductase genes causes moderate and high-level metronidazole resistance in Helicobacter pylori

AU - Jeong, J. Y.

AU - Mukhopadhyay, A. K.

AU - Dailidiene, D.

AU - Wang, Y.

AU - Velapatino, B.

AU - Gilman, Robert H

AU - Parkinson, A. J.

AU - Nair, G. B.

AU - Wong, B. C Y

AU - Shiu Kum Lam, Kum Lam

AU - Mistry, R.

AU - Segal, I.

AU - Yuan, Y.

AU - Gao, H.

AU - Alarcon, T.

AU - Brea, M. L.

AU - Ito, Y.

AU - Kersulyte, D.

AU - Lee, H. K.

AU - Gong, Y.

AU - Goodwin, A.

AU - Hoffman, P. S.

AU - Berg, D. E.

PY - 2000

Y1 - 2000

N2 - Helicobacter pylori is a human-pathogenic bacterial species that is subdivided geographically, with different genotypes predominating in different parts of the world. Here we test and extend an earlier conclusion that metronidazole (Mtz) resistance is due to mutation in rdxA (HP0954), which encodes a nitroreductase that converts Mtz from prodrug to bactericidal agent. We found that (i) rdxA genes PCR amplified from 50 representative Mtz(r) strains from previously unstudied populations in Asia, South Africa, Europe, and the Americas could, in each case, transform Mtz(s) H. pylori to Mtz(r); (ii) Mtz(r) mutant derivatives of a cultured Mtz(s) strain resulted from mutation in rdxA; and (iii) transformation of Mtz(s) strains with rdxA-null alleles usually resulted in moderate level Mtz resistance (16 μg/ml). However, resistance to higher Mtz levels was common among clinical isolates, a result that implicates at least one additional gene. Expression in Escherichia coli of frxA (HP0642; flavin oxidoreductase), an rdxA paralog, made this normally resistant species Mtz(s), and frxA inactivation enhanced Mtz resistance in rdxA-deficient cells but had little effect on the Mtz susceptibility of rdxA+ cells. Strains carrying frxA-null and rdxA-null alleles could mutate to even higher resistance, a result implicating one or more additional genes in residual Mtz susceptibility and hyperresistance. We conclude that most Mtz resistance in H. pylori depends on rdxA inactivation, that mutations in frxA can enhance resistance, and that genes that confer Mtz resistance without rdxA inactivation are rare or nonexistent in H. pylori populations.

AB - Helicobacter pylori is a human-pathogenic bacterial species that is subdivided geographically, with different genotypes predominating in different parts of the world. Here we test and extend an earlier conclusion that metronidazole (Mtz) resistance is due to mutation in rdxA (HP0954), which encodes a nitroreductase that converts Mtz from prodrug to bactericidal agent. We found that (i) rdxA genes PCR amplified from 50 representative Mtz(r) strains from previously unstudied populations in Asia, South Africa, Europe, and the Americas could, in each case, transform Mtz(s) H. pylori to Mtz(r); (ii) Mtz(r) mutant derivatives of a cultured Mtz(s) strain resulted from mutation in rdxA; and (iii) transformation of Mtz(s) strains with rdxA-null alleles usually resulted in moderate level Mtz resistance (16 μg/ml). However, resistance to higher Mtz levels was common among clinical isolates, a result that implicates at least one additional gene. Expression in Escherichia coli of frxA (HP0642; flavin oxidoreductase), an rdxA paralog, made this normally resistant species Mtz(s), and frxA inactivation enhanced Mtz resistance in rdxA-deficient cells but had little effect on the Mtz susceptibility of rdxA+ cells. Strains carrying frxA-null and rdxA-null alleles could mutate to even higher resistance, a result implicating one or more additional genes in residual Mtz susceptibility and hyperresistance. We conclude that most Mtz resistance in H. pylori depends on rdxA inactivation, that mutations in frxA can enhance resistance, and that genes that confer Mtz resistance without rdxA inactivation are rare or nonexistent in H. pylori populations.

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