Abstract
Vibrio cholerae causes epidemic diarrhea throughout the world. Fluid replacement is the primary therapy for cholera; however, high mortality rates often necessitate the use of antibiotics. V. cholerae, like most bacteria, has developed resistance to some antibiotics. In the early 1990s a new serotype strain, Bengal 0139, began a new wave of cholera epidemics. Bengal isolates showed unique trends in antimicrobial resistance. Many clinical laboratories use automated antibiotic susceptibility testing for V. cholerae. It is important to know if automated susceptibility test results for V. cholerae coincide with reported trends in antibiotic susceptibility. In the present study, we used the Vitek automated susceptibility system to determine the susceptibilities of 79 V. cholerae O1 isolates, 100 O139 isolates, and 112 non-O1 isolates. Vitek susceptibilities for V. cholerae showed a good correlation with preestablished epidemiological data. Although the new O139 serogroup showed a trend of increased resistance to trimethoprim-sulfamethoxazole and nitrofurantoin, it was more susceptible to ampicillin than previous serogroup O1 and non-O1 strains. Regardless of serogroup, > or = 98% of the V. cholerae isolates tested were susceptible to most antibiotics tested by us. It is important to continue susceptibility testing of all new isolates of V. cholerae because of emerging resistant strains. However, V. cholerae remains susceptible to most of the available antibiotics.
MeSH Terms
Cholera/drug therapy,epidemiology,microbiology
Disease Outbreaks
Drug Resistance, Microbial
Drug Resistance, Multiple
Evaluation Studies as Topic
Humans
Microbial Sensitivity Tests/methods
Serotyping
Species Specificity
Vibrio cholerae/classification,drug effects,isolation & purification
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sciortino C V
Department of Veterans Affairs Medical Center, Louisville, Kentucky, USA.
Johnson J A
Hamad A
References (16)
16 references, click to expand
-
Controlled comparison of tetracycline and furazolidone in cholera.
Br Med J. 1968 Aug 3;3(5613):277-80
PMID: 4873660
-
New variant of Vibrio cholerae O1 from clinical isolates in Amazonia.
J Clin Microbiol. 1995 Jan;33(1):114-8
PMID: 7535309
-
Effect of chemotherapy on the duration of diarrhoea, and on vibrio excretion by cholera patients.
J Trop Med Hyg. 1971 Aug;74(8):172-6
PMID: 4936576
-
Rapid emergence of El Tor Vibrio cholerae resistant to antimicrobial agents during first six months of fourth cholera epidemic in Tanzania.
Lancet. 1979 Feb 17;1(8112):345-7
PMID: 85001
-
Emergence of multiply antibiotic-resistant Vibrio cholerae in Bangladesh.
J Infect Dis. 1980 Dec;142(6):939-42
PMID: 7462703
-
Vibrio cholerae El Tor acquires plasmid-encoded resistance to gentamicin.
Lancet. 1982 Jan 2;1(8262):42
PMID: 6119431
-
Monoclonal antibodies to outer membrane antigens of Vibrio cholerae.
Infect Immun. 1985 Jul;49(1):122-31
PMID: 3159676
-
In vitro susceptibility of pathogenic Vibrio species to norfloxacin and six other antimicrobial agents.
Antimicrob Agents Chemother. 1985 Sep;28(3):442-5
PMID: 4073866
-
Epidemiology of antimicrobial resistant cholera in Kenya and East Africa.
Am J Trop Med Hyg. 1988 Nov;39(5):484-90
PMID: 3195696
-
Non-O group 1 Vibrio cholerae: a look at the epidemiology of an occasional pathogen.
Epidemiol Rev. 1990;12:179-91
PMID: 2286218
-
Emergence of novel strain of Vibrio cholerae with epidemic potential in southern and eastern India.
Lancet. 1993 Mar 13;341(8846):703-4
PMID: 8095620
-
Large outbreak of clinical cholera due to Vibrio cholerae non-O1 in Bangladesh.
Lancet. 1993 Mar 13;341(8846):704
PMID: 8095621
-
Vibrio cholerae non-O1--the eighth pandemic?
Lancet. 1993 Aug 14;342(8868):382-3
PMID: 8101894
-
Vibrio cholerae O139 Bengal.
J Clin Microbiol. 1994 Oct;32(10):2345-9
PMID: 7814463
-
Survey of in vitro susceptibilities of Vibrio cholerae O1 and O139 to antimicrobial agents.
Antimicrob Agents Chemother. 1995 Jan;39(1):241-4
PMID: 7695314
-
Optimal antibiotic therapy in cholera.
Bull World Health Organ. 1968;39(2):239-45
PMID: 4881071