Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 11, Number 1—January 2005
Letter

Fluoroquinolone-resistant Salmonella Paratyphi A

On This Page
Tables
Article Metrics
24
citations of this article
EID Journal Metrics on Scopus

Cite This Article

To the Editor: Fluoroquinolones have been the drug of choice for treating typhoid and paratyphoid fever since the beginning of the 1990s. Multidrug-resistant strains began to prevail in disease-endemic areas, and former first-line antimicrobial drugs, such as chloramphenicol, were sometimes ineffective (1). In recent years, however, strains with decreased susceptibility to quinolones have emerged, and clinical treatment failure is a serious concern (25).

An 87-year-old woman was referred from a local clinic to Yokohama Municipal Citizen’s Hospital in July 2002 because Salmonella enterica serovar Paratyphi A was detected in her urine. She had no subjective symptoms such as pain on urination or urinary urgency, and her temperature was normal. She had never had paratyphoid fever, and she had not traveled abroad. No other person in the community had paratyphoid. Before being admitted to the hospital, she had experienced frequent episodes of urinary tract infection and had been empirically treated each time with oral antimicrobial drugs, including ciprofloxacin. She had been given a dose of 600 mg/day for 7 days, 25 times in the last 4 years.

The patient did not display any abnormal findings on physical examination. S. Paratyphi A was not detected in the urine but was confirmed in the stool; therefore, the previous report of bacteriuria could have been due to contamination of a urine sample with feces. An ultrasound showed a polyp and multiple stones in her gallbladder. A carrier state was suspected. Bile was obtained by duodenal aspiration and was positive for S. Paratyphi A. The patient was considered to be an asymptomatic cholecystic carrier of S. Paratyphi A.

On disk diffusion susceptibility testing, the isolate was resistant to nalidixic acid (NA) and to ofloxacin. The MIC of ofloxacin was as high as 256 µg/mL, and the MIC of ciprofloxacin was128 µg/mL (Table). An open cholecystectomy was performed for treatment of the polyp, the stones, and the highly quinolone-resistant bacteria. A routine perioperative intravenous antimicrobial agent, cefmetazole, was administered as surgical prophylaxis. The polyp was malignant, and the operation was curative. The patient resumed normal activities, and had no further fecal excretion of S. Paratyphi A.

Polymerase chain reaction (PCR) amplification and DNA sequencing were conducted to detect mutations responsible for the fluoroquinolone resistance. Nucleotide sequences of gyrA, gyrB, parC, and parE genes were investigated. The primers used for PCR amplification and DNA sequencing have been previously described (6,7). An ABI Prism dye terminator cycle sequencing kit (Perkin-Elmer, Applied Biosystems, Foster City, CA) and an automated sequencer (311A; Perkin-Elmer, Applied Biosystems) were used. The isolated strain possessed triple point mutations. The first 2 mutations were in the gyrA gene, which encodes DNA gyrase, at codon 83 (TCC to TTC), which substitutes phenylalanine for serine, and at codon 87 (GAC to AAC), which substitutes asparagine for aspartic acid. The third mutation was in the parC gene, which encodes DNA topoisomerase IV, at codon 84 (GAA to AAA), which substitutes lysine for glutamic acid. No mutations were found in gyrB and pare E.

S. Typhi and Paratyphi A with decreased susceptibility to fluoroquinolones emerged on the Indian subcontinent, Southeast Asia, and Central Asia in the mid-1990s (25). On disk diffusion testing, these strains were NA-resistant, and susceptible to ofloxacin or ciprofloxacin; however, the MICs of ciprofloxacin increased to 0.25–4 μg/mL, 10- to 100-fold higher than the usual NA–susceptible strains (5,8,9). NA-resistant strains of S. Typhi have 1 point mutation at the target site of quinolones, DNA gyrase, in the quinolone resistance–determining region of gyrA, either at codon 83 or codon 87 (2,3). Several epidemics of typhoid and paratyphoid fever caused by NA-resistant strains with clinical failure of quinolone treatment have been reported (4,5).

An experimental attempt had been previously made to induce the production of strains with high-level fluoroquinolone resistance by culturing strains of S. Typhi and Paratyphi A in ciprofloxacin-supplemented medium (7). One of these in vitro–induced, high-level resistant strains of S. Paratyphi A had triple mutations in the gyrA gene at codons 83 and 87 and in the parC gene at codon 84, which are the same triple mutations as those seen in the current in vivo case.

Full fluoroquinolone resistance has already emerged in the community in nontyphoid Salmonella species. In a clinical isolate of S. enterica serovar Typhimurium, the MIC of ciprofloxacin was 32 µg/mL, and mutations in both gyrA and gyrB were noted (10).

Our findings strongly suggest that high-level quinolone resistance was induced through the long-term carrier state of S. Paratyphi A under selective pressure of frequent quinolone administration. The resistance is associated with the 2 mutation sites in gyrA and 1 site in parC, and multiple point mutations are likely related to the acquisition of full resistance. Physicians should be aware of the emergence of S. Typhi and Paratyphi A, as well as nontyphoid Salmonella species, which are highly quinolone-resistant.

Top

Takuya Adachi*Comments to Author , Hiroko Sagara*, Kenji Hirose†, and Haruo Watanabe†
Author affiliations: *Yokohama Municipal Citizen’s Hospital, Yokohama, Japan; †National Institute of Infectious Diseases, Tokyo, Japan

Top

References

  1. Rowe  B, Threlfall  EJ, Ward  LR. Spread of multiresistant Salmonella typhi. Lancet. 1990;336:1065. DOIPubMedGoogle Scholar
  2. Brown  JC, Shanahan  PM, Jesudason  MV, Thomson  CJ, Amyes  SG. Mutations responsible for reduced susceptibility to 4-quinolones in clinical isolates of multi-resistant Salmonella typhi in India. J Antimicrob Chemother. 1996;37:891900. DOIPubMedGoogle Scholar
  3. Wain  J, Hoa  NTT, Chinh  NT, Vinh  H, Everett  MJ, Diep  TS, Quinolone-resistant Salmonella typhi in Viet Nam: molecular basis of resistance and clinical response to treatment. Clin Infect Dis. 1997;25:140410. DOIPubMedGoogle Scholar
  4. Murdoch  DA, Banatvala  NA, Bone  A, Shiosmatulloev  BI, Ward  LR, Threlfall  EJ. Epidemic ciprofloxacin-resistant Salmonella typhi in Tajikistan. Lancet. 1998;351:339. DOIPubMedGoogle Scholar
  5. Chandel  DS, Chaudhry  R, Dhawan  B, Pandey  A, Dey  AB. Drug-resistant Salmonella enterica serotype Paratyphi A in India. Emerg Infect Dis. 2000;6:4201. DOIPubMedGoogle Scholar
  6. Giraud  E, Brisabois  A, Martel  JL, Chaslus-Dancla  E. Comparative studies of mutations in animal isolates and experimental in vitro- and in vivo- selected mutants of Salmonella spp. suggest a counterselection of highly fluororquinolone-resistant strains in the field. Antimicrob Agents Chemother. 1999;43:21317.PubMedGoogle Scholar
  7. Hirose  K, Hashimoto  A, Tamura  K, Kawamura  Y, Ezaki  T, Sagara  H, DNA sequence analysis of DNA gyrase and DNA topoisomerase IV quinolone resistance–determining regions of Salmonella enterica serovar Typhi and serovar Paratyphi A. Antimicrob Agents Chemother. 2002;46:324952. DOIPubMedGoogle Scholar
  8. Atkins  BL, Gottlieb  T. Emerging drug resistance and vaccination for typhoid fever [letter]. JAMA. 1998;279:57980. DOIPubMedGoogle Scholar
  9. Threlfall  EJ, Skinner  JA, Ward  LR. Detection of decreased in vitro susceptibility to ciprofloxacin in Salmonella enterica serotypes Typhi and Paratyphi A. J Antimicrob Chemother. 2001;48:7401. DOIPubMedGoogle Scholar
  10. Heisig  P. High-level fluoroquinolone resistance in a Salmonella typhimurium isolate due to alterations in both gyrA and gyrB genes. J Antimicrob Chemother. 1993;32:36777. DOIPubMedGoogle Scholar

Top

Table

Top

Cite This Article

DOI: 10.3201/eid1101.040145

Related Links

Top

Table of Contents – Volume 11, Number 1—January 2005

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Takuya Adachi, 56 Okazawacho, Hodogaya-Ku, Yokohama 240-8555, Japan; fax: +81-45-331-1960

Send To

10000 character(s) remaining.

Top

Page created: April 14, 2011
Page updated: April 14, 2011
Page reviewed: April 14, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external