Quinolone-resistant Salmonella typhi in Viet Nam: Molecular basis of resistance and clinical response to treatment: Molecular basis of resistance and clinical response to treatment

  • John Wain
  • , Nguyen T.T. Hoa
  • , Nguyen T. Chinh
  • , Ha Vinh
  • , Martin J. Everett
  • , To S. Diep
  • , Nicholas P.J. Day
  • , Tom Solomon
  • , Nicholas J. White
  • , Laura J.V. Piddock
  • , Christopher Parry

Research output: Contribution to journalArticlepeer-review

298 Citations (Scopus)

Abstract

Nalidixic acid-resistant Salmonella typhi (NARST) was first isolated in Viet Nam in 1993. Analysis of the quinolone resistance-determining region of gyrA in 20 NARST isolates by polymerase chain reaction and single-stranded conformational polymorphism yielded two novel patterns: pattern II corresponding to a point mutation at nucleotide 87 Asp → Gly (n = 17), and pattern III corresponding to a point mutation at nucleotide 83 Set → Phe (n = 3). In trials of short-course ofloxacin therapy for uncomplicated typhoid, 117 (78%) of 150 patients were infected with multidrug-resistant S. typhi, 18 (15%) of which were NARST. The median time to fever clearance was 156 hours (range, 30-366 hours) for patients infected with NARST and 84 hours (range, 12-378 hours) for those infected with nalidixic acid-susceptible strains (P < .001). Six (33.3%) of 18 NARST infections required retreatment, whereas 1 (0.8%) of 132 infections due to susceptible strains required retreatment (relative risk = 44; 95% confidence interval = 5.6-345; P < .0001). We recommend that short courses of quinolones not be used in patients infected with NARST.
Original languageEnglish
Pages (from-to)1404-1410
Number of pages7
JournalClinical Infectious Diseases
Volume25
Issue number6
DOIs
Publication statusPublished - 1 Jan 1997

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