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3.
J Hyg ; 71(1): 209-15, Mar. 1973.
Article in English | MedCarib | ID: med-15804

ABSTRACT

The antibiotic resistance patterns of califorms in faecal specimens from pigs and their human contacts were studied. The ability of the resistant coliforms to transfer their resistance in vitro to antibiotic-sensitive recipients was examined. The results showed that pigs which had received antibiotics carried more multiply-resistant, R-factor bearing coliforms than pigs which had not been given antibiotics. Human contacts of the antibiotic-treated pigs had a higher incidence of antibiotic-resistant coliforms with R-factors than contacts of pigs which had not been given antibiotics. It is concluded that antibiotic treatment of farm animals may lead to acquisition of antibiotic resistance by gut coliforms of man.(AU)


Subject(s)
Humans , 21003 , Extrachromosomal Inheritance , Penicillin Resistance , Swine Diseases/microbiology , Zoonoses , Ampicillin , Chloramphenicol , Disease Reservoirs , Feces/microbiology , Streptomycin , Sulfonamides , Swine , Tetracycline
4.
Kingston; s.n; June 1970. 114 p. tab.
Thesis in English | MedCarib | ID: med-13627

ABSTRACT

Resistance factors, the transmissible genetic elements which confer drug resistance on members of the Enterobacteriaceae, are frequently found in isolates from human specimens. It was suggested that farm animals which receive antibiotics might harbour these R factors and infect the human community by way of the farm workers who handle them. In this study, a total of 252 faecal specimens were collected - 152 from pigs and employees on a farm using antibiotics, and 100 from pigs and employees on control farms using no antibiotics. An E. coli culture was selected from each specimen and examined for resistance to: Ampicillin, Sulphonamide, Streptomysin, Chloramphenicol, Tetracycline, Nalidixic Acid. Resistance cultures were further examined for the ability to transfer drug resistance to sensitive bacteria. 1. 110 faecal specimens were collected from the test pigs which had been given antibiotics. All the specimens yielded multiply resistance E. coli of which 94 (86 percent) were able to transfer all or part of their resistance pattern to a suitable sensitive recipient. 2. 42 humans in contact with the test pigs were examined in the same manner. 86 percent of the isoaltes were resistant to one or more of the drugs and 48 percent transferred drug resistance. 3. Specimens were collected from 72 pigs in the control group. 68 (94 percent) contained drug resistant E. coli of which 16 (22 percent) transferred their resistance. 4. 20 out of 28 humans (i.e. 72 percent) in the control group yielded resistant E. coli and six (21 percent) transferred their resistance. The results indicate that: I. Those pigs exposed to antibiotics harboured coliforms with R factors more frequently than pigs not exposed to antibiotics. II. The control human group also had a lower occurrence of transmissible drug resistance than the group who worked with the antibiotic-treated pigs. III. The relatives of the farm employees excreted more transmissible drug resistant strain (43 percent) than the human control group (21 percent). IV. The highest incidence of transmissible drug resistant strains was among individuals who were taking antibiotics at the same time the specimens were collected. Pigs which had not been given antibiotics for some months showed a lower yield of transmissible drug resistant strains than those currently taking antibiotics at the time the specimens were collected. V. The humans from the test farm, although they were not currently taking antibiotics, yielded drug resistant strains at a rate comparable to the test pigs. However, only 48 percent of these transferred drug resistance, compared with 86 percent of the test pigs. VI. Drug resistant bacteria were found in the majority of specimens from all groups, but the ability to transfer these resistances varied widely (Summary)


Subject(s)
Humans , 21003 , Escherichia coli/immunology , Anti-Bacterial Agents/immunology , Drug Resistance, Microbial/immunology , R Factors/immunology , Feces/microbiology , Rural Population , F Factor/immunology , Swine/immunology
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