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

被引:233
作者
Wain, J
Hoa, NTT
Chinh, NT
Vinh, H
Everett, MJ
Diep, TS
Day, NPJ
Solomon, T
White, NJ
Piddock, LJV
Parry, CM
机构
[1] Wellcome Trust, Ctr Trop Dis, Clin Res Unit, Ho Chi Minh City, Vietnam
[2] Cho Quan Hosp, Ctr Trop Dis, Ho Chi Minh City, Vietnam
[3] Sch Med, Dept Infect Dis, Ho Chi Minh City, Vietnam
[4] John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Trop Med, Oxford OX3 9DU, England
[5] Univ Birmingham, Dept Infect, Antimicrobial Agents Res Grp, Birmingham, W Midlands, England
基金
英国惠康基金;
关键词
D O I
10.1086/516128
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 Ser --> 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.
引用
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页码:1404 / 1410
页数:7
相关论文
共 30 条
[1]  
Ausubel F.M., 1996, CURRENT PROTOCOLS MO
[2]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[3]   Effects on growth of single short courses of fluoroquinolones [J].
Bethell, DB ;
Hien, TT ;
Phi, LT ;
Day, NPJ ;
Vinh, H ;
Duong, NM ;
VanLen, N ;
VanChuong, L ;
White, NJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 74 (01) :44-46
[4]   Pharmacokinetics of oral and intravenous ofloxacin in children with multidrug-resistant typhoid fever [J].
Bethell, DB ;
Day, NPJ ;
Dung, NM ;
McMullin, C ;
Loan, HT ;
Tam, DTH ;
Minh, LTN ;
Linh, NTM ;
Dung, NQ ;
Vinh, H ;
MacGowan, AP ;
White, LO ;
White, NJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (09) :2167-2172
[5]  
BINH H, 1996, ANTIMICROB AGENTS CH, V40, P958
[6]  
Biswal N, 1994, Indian Pediatr, V31, P229
[7]   Mutations responsible for reduced susceptibility to 4-quinolones in clinical isolates of multi-resistant Salmonella typhi in India [J].
Brown, JC ;
Shanahan, PMA ;
Jesudason, MV ;
Thomson, CJ ;
Amyes, SGB .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 (05) :891-900
[8]   Mutations of the gyrA gene of clinical isolates of Salmonella typhimurium and three other Salmonella species leading to decreased susceptibilities to 4-quinolone drugs [J].
Brown, JC ;
Thomson, CJ ;
Amyes, SGB .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 (02) :351-356
[9]  
CHANDRA R, 1992, J TROP MED HYG, V95, P284
[10]   Short courses of ofloxacin for the treatment of enteric fever [J].
Chinh, NT ;
Solomon, T ;
Thong, MX ;
Ly, NT ;
Hoa, NTT ;
Wain, J ;
Diep, TS ;
Smith, MD ;
Day, NPJ ;
Phi, LT ;
Parry, C ;
White, NJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1997, 91 (03) :347-349