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Caprylate-thallous Agar Medium for Selectively Isolating Serratia and Its Utility in the Clinical Laboratory

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Specialty Microbiology
Date 1976 Sep 1
PMID 972193
Citations 18
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Abstract

A defined agar medium (hereinafter designated caprylate-thallous [CT5 agar) containing 0.01% yeast extract, 0.1% caprylic (n-octanoic) acid, and 0.025% thallous sulfate is highly selective for all Serratia species and effectively discriminates against most non-Serratia strains likely to be in the same habitats. The selectivity of CT agar is demonstrated by the very high efficiency of colony formation (mean, 80.7% of that on a nonselective complex medium) on CT agar by known Serratia strains and the very low efficiency of colony formation (close to zero) on CT agar by bacterial strains known not to be Serratia. The utility of this medium in actual clinical laboratory practice is demonstrated by the more rapid and higher recovery of Serratia on this selective medium as compared to conventional procedures of in-tandem runs of 513 consecutive urine, feces, and sputum specimens. Pigmented and nonpigmented Serratia strains deliberately added to fecal specimens can be selectively and quantitatively recovered on CT agar. CT agar compares favorably with, or in some cases is an improvement over, other selective media which have been recommended for isolating Serratia. This selective CT agar medium could be quite useful in ecological surveys, especially those related to hospital-acquired infections.

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References
1.
LANCASTER L . Role of Serratia species in urinary tract infections. Arch Intern Med. 1962; 109:536-9. DOI: 10.1001/archinte.1962.03620170034005. View

2.
WHEAT R, Zuckerman A, RANTZ L . Infection due to chromobacteria; report of 11 cases. AMA Arch Intern Med. 1951; 88(4):461-6. DOI: 10.1001/archinte.1951.03810100045004. View

3.
Wilson C, Slavin G . A direct culture method for the examination of milk samples. J Comp Pathol. 1950; 60(3):230-4. DOI: 10.1016/s0368-1742(50)80022-x. View

4.
CABRERA H . An outbreak of Serratia marcescens, and its control. Arch Intern Med. 1969; 123(6):650-5. View

5.
RAGAZZINI F, LA CAUZA C, Ferrucci M . Infection by Serratia marcescens in premature children. Ann Paediatr. 1965; 205(4):289-300. View