Sudan Journal of Medical Sciences (Apr 2017)

Molecular Diagnosis of Shigella, Salmonella and Campylobacter by Multiplex Real-Time PCR in Stool Culture Samples in Ouagadougou (Burkina Faso)

  • Salfo Sawadogo,
  • Msc,
  • Engineer1comma2,
  • Birama Diarra,
  • PharmD,
  • Msc,
  • PhD Student,
  • Cyrille Bisseye,
  • PhD,
  • Assistant Professor,
  • Tegwindé Rebeca Compaore,
  • PhD,
  • assistant researcher,
  • Florencia W. Djigma,
  • PhD,
  • Assistant Professor,
  • Djénéba Ouermi,
  • PhD,
  • assistant Professor,
  • Aboubakar S. Ouattara,
  • PhD,
  • Full Professor,
  • Jacques Simporé,
  • PhD,
  • Full Professor

DOI
https://doi.org/10.18502/sjms.v12i3.931
Journal volume & issue
Vol. 2017
pp. 1 – 11

Abstract

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Background: Bacteriological diagnosis of Campylobacter spp, Salmonella spp and Shigella sppcould be necessary in case of infectious gastroenteritis syndrome. The objective of this study was to diagnose concomitantly the three enteropathogenic bacteria by multiplex Real-Time PCR in stool culture samples in Ouagadougou (Burkina Faso). Materials and Methods: The study was conducted from February 5th to March 9th, 2013. Two hundred stool samples were received during the study period. The bacteria were identified by bacterial culture following by multiplex Real-Time PCR. Results: Shigella spp and Campylobacter spp were sought by culture in all 200 samples. Enteropathogenic E. coli was sought only in 37 samples from all children under 2 years old. The bacterial culture was positive in 12 stool samples. Shigella spp and Salmonella spp. were isolated respectively in 5 (2.5%) and 3 samples (1.5%). Enteropathogenic E. coli was isolated in 10.8% (4/37) of the samples tested. The multiplex real-time PCR identified bacteria in 20 patients, including 17 cases of Shigella spp., 1 case of Salmonella spp. and 2 cases of Campylobacter spp. Conclusions: This study has highlighted the low frequency of 3 sought bacterial genera in stool samples. It has also demonstrated a significant difference between the culture and the multiplex Real-Time PCR method in the diagnosis of Shigella.

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