Detection by Culture and by Multiplex Real-Time PCR of Staphylococcus aureus and Staphylococcus spp. in Vaginal Secretions and Urines in Patients Received at Saint Camille Hospital of Ouagadougou, Burkina Faso

Nikiema, Rabiétou and Zohoncon, Théodora M. and Bado, Prosper and Guigma, Geraud Joel and Dabiré, Amana Metuor and Simpore, Jacques (2024) Detection by Culture and by Multiplex Real-Time PCR of Staphylococcus aureus and Staphylococcus spp. in Vaginal Secretions and Urines in Patients Received at Saint Camille Hospital of Ouagadougou, Burkina Faso. Current Journal of Applied Science and Technology, 43 (3). pp. 90-100. ISSN 2457-1024

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Abstract

Staphylococci are bacteria involved in various pathologies and varying degrees of severity. They are one of the first causative agents of nosocomial and community infections with humans and animals as natural habitats. The genus Staphylococcus is subdivided into two groups, coagulase-negative staphylococci, the most isolated of which is Staphylococcus aureus and coagulase-positive staphylococci and constitutes about fifty species and subspecies. Some of these species are implicated in urinary tract and vaginal tract infections and are a real health problem especially for women. The aim of the study was to detect S. aureus and Staphylococcus spp. in vaginal secretions and urine using culture and real-time PCR. The microbiological analysis was done using the conventional methods adopted at Saint Camille's hospital laboratory. Molecular analysis was done using the Sacace multiplex PCR kit.

We examined a total of 97 samples including 77 urine samples and 20 vaginal secretion samples. At culture, no Staphylococcus was isolated. On the other hand, with the same culture-negative samples, we were able to identify two S. aureus and two Staphylococcus spp. in the urine and three Staphylococcus spp in vaginal secretions. The study then demonstrates the difference in sensitivity between the two identification techniques and confirms that there is a possibility of infection in case of negative culture. It is then necessary to involve rt-PCR in routine analyses.

Item Type: Article
Subjects: Archive Paper Guardians > Multidisciplinary
Depositing User: Unnamed user with email support@archive.paperguardians.com
Date Deposited: 02 Mar 2024 06:37
Last Modified: 02 Mar 2024 06:37
URI: http://archives.articleproms.com/id/eprint/2678

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