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  Afr. J. Biotechnol.

  Vol. 8 No. 22

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  Search Pubmed for articles by:

  Ramalivhana NJ
  Obi CL

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African Journal of Biotechnology Vol. 8 (22), pp. 6388-6392, 16 November 2009

ISSN 1684-5315  © 2009 Academic Journals  

 

 

Full Length Research Paper

 

Plesiomonas shigelloides in stool samples of patients in the Venda Region: Possible considerations on pathogenicity and antibiogram profiles

 

Ramalivhana, N. J.1 and Obi, C. L.2*

 

1College of Agriculture and Environmental Sciences, University of South Africa, P.O. Box 392, Pretoria. 0003, South Africa.

2Academic and Research Directorate, Walter Sisulu University, Nelson Mandela Drive, Mthatha, Eastern Cape, South Africa.

 

*Corresponding author. E-mail: c355251@yahoo.com.

 

Accepted 18 April, 2008

 

   Abstract

 

This study determined the haemolytic, haemagglutinating and antibiotic susceptibility activities of Plesiomonas shigelloides isolated from stool samples of patients attending different health centers in the Venda region of South Africa. P. shigelloides was isolated and identified using the API 20E, API 20NE systems. Antibiotic susceptibility profiles of the isolates were determined using the disc diffusion method and analyzed according to NCCLS standards. The hemolytic and hemagglutination activities of the isolates on human, sheep, pig and chicken red blood cells were determined using the plate and slide methods. A total of 89 (13%) P. shigelloide were isolated from 660 samples. The hemolytic activities of the isolates were variable with no heamolysis on sheep red cells. 33 (37%) of isolates were beta lactamase producers. There was a high level of resistance to the penicilllins with 100% resistance to Penicillin G, Amoxicillin and Ampicillin. This study has demonstrated multiple resistance to different antibiotics and production of beta lactamase. Most of the isolates showed evidence of pathogenicity as demonstrated by hemolytic and haemagglutinating activities.

 

Key words: Plesiomonas shigelloides, stool samples, antibiograms, red blood cells, pathogenicity, haemolysis, haemagglutination.

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