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Assessment of the Presence of Resistance Genes Detected from the Environment and Selected Food Products in Benin
Author(s) -
Victorien Doug,
Vincentia Marie Camille Houssou,
Eugénie Anago,
Chimène Nanoukon,
Jibril Mohammed,
Alidéhou Jerrold Agbankpé,
Hornel Koudokpon,
Birikissou Bouraima,
Esther Dégué,
Kafayath Fabiyi,
Marie Hidjo,
Fidélia Djegui,
Lamine BabaMoussa,
Martin Pépin Aïna
Publication year - 2021
Publication title -
journal of environmental and public health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.869
H-Index - 35
eISSN - 1687-9813
pISSN - 1687-9805
DOI - 10.1155/2021/8420590
Subject(s) - bacilli , microbiology and biotechnology , virulence , biology , pseudomonas aeruginosa , agar , multiple drug resistance , agar diffusion test , polymerase chain reaction , food science , escherichia coli , antibiotics , bacteria , gene , veterinary medicine , medicine , genetics
Gram-negative bacilli can spread from the environment and through food products. This study aimed to characterize ESBL production and virulence genes from multidrug-resistant Gram-negative bacilli isolated from specimen collected from the environment, kitchen, and food products. A total of 130 samples were collected at local markets in seven different communities in Benin (Abomey-Calavi, Ouidah, Bohicon, Abomey, Parakou, Djougou, and Grand-Popo). Samples were cultured on McConkey and ChromID ™ ESBL agar plates. The isolates were identified by the API 20E gallery. An antibiotic susceptibility test was carried out, and the detection of ESBL production and virulence-associated genes was carried out by Polymerase Chain Reaction (PCR). The data collected was coded and analyzed using GraphPad prism 7 software and Excel. The software R was used to calculate the correlation coefficient between the results of the detection of ESBL+ on agar and by the effect of the double synergy. The results showed that sixty-three (63) bacterial strains were isolated from the 130 samples, of which the dominant species was Chryseomonas luteola (10/63). The kitchen samples were the most contaminated with 36.50%. More than 40% of the isolates were resistant to at least three different classes of antibiotics. Also, blaSHV gene was detected in 33.33% (21/63) of the isolates and in all isolates of Pseudomonas aeruginosa (5/5%). 11.11% (7/63) of isolates were virulent with dominance of the fim H gene, especially with Escherichia coli (83.33%). The kitchen samples showed a high prevalence of ESBL-producing strains with fim H gene. This raises the problem of non-compliance with hygiene rules in community cooking and food handling.

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