Isolation and identification of autoagglutinating serogroup O:11 Aeromonas strains in the clinical laboratory

Author:

Kokka R P1,Janda J M1

Affiliation:

1. Microbial Diseases Laboratory, California Department of Health Services, Berkeley 94704.

Abstract

We evaluated the extent to which serogroup O:11 Aeromonas strains could be recovered from both clinical and environmental specimens and the cultural parameters that affected the phenotypic marker (autoagglutination) associated with this group. Of over 200 Aeromonas strains screened, serogroup O:11 was identified only among the phenospecies A. hydrophila and A. sobria and was associated with clinical isolates more frequently than with environmental strains. Blood and wound isolates accounted for almost 50% of all O:11 strains identified. The autoagglutination phenotype associated with O:11 strains could be detected in most commercial liquid media, under a wide range of growth temperatures, and within 15 min of incubation at 100 degrees C. The results suggest that clinical laboratories can recognize this important group of Aeromonas strains by two simple tests.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference11 articles.

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3. Surface protein composition of Aeromonas hydrophila strains virulent for fish: identification of a surface array protein;Dooley J. S. G.;J. Bacteriol.,1988

4. Congo red agar, a differential medium for Aeromonas salmonicida, detects the presence of the cell surface protein array involved in virulence;Ishiguro E. E.;J. Bacteriol.,1985

5. Janda J. M. 1987. Aeromonas and Plesiomonas infections p. 37-44. In B. Wentworth (ed.) Diagnostic procedures for bacterial infections 7th ed. American Public Health Association Washington D.C.

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