Open Access Open Access  Restricted Access Subscription Access

Assessment of Foods and Drinks for the Presence of Extended Spectrum Beta Lactamase (ESBL) Producing Bacteria in Gombe Metropolis, Nigeria


Affiliations
1 Department of Food Service and Management, Faculty of Food Science and Technology University Putra Malaysia,43400 Serdang, Selangor Darul Ehsan, Malaysia
2 Department of Microbiology, Gombe State University, P.M.B. 127, Gombe State, Nigeria
3 Department of Microbiology, Bayero University Kano, P.M.B. 3011, Kano State, Nigeria
4 College of Health sciences, Maryam Abacha American University of Niger, ADS Avenue, Roy Mohd VI, Du Maroc, Maradi, Republic Du Niger
5 Faculty of Chemical Engineering and Natural Resources, University Malaysia Pahang,26300 Gambang, Pahang, Malaysia
 

Objectives: To make preliminary screening study for the presence of ESBL producing bacteria, in food and drinks sold in Gombe metropolis. 30 samples of food and drinks were collected and analyzed. Method: Bacterial isolation was performed on nutrient agar and identification started from gram staining; the gram negative isolates obtained, among which ESBL producers were found and further subjected to standard biochemical tests and confirmed to be enterobacteriaceae. They were then screened for ESBLs in accordance with Clinical and Laboratory Standard Institute (CLSI) breakpoint, and the suspected ESBLs bacteria were confirmed using double disc synergy testing (DDST) with standard Augmentin (Amoxycillin/ Clavulanic Acid, 30μg; Oxoid England, CT0223B), Ceftriaxone (CRO 30μg; Oxoid England, CT0417B) and Ceftazidime (CAZ 30μg; Oxoid England, CT0412B). Findings: The fourteen 14(100%) Gram negative bacteria isolated were found to include Pseudomonasaeruginosa 2(14.29%) and members of the family Enterobacteriaceae (enteric gram negative rods): Citrobacterfreundii 2(14.29%), Enterobacterspp. 1(7.14%), Escherichiacoli 4(28.57%), Klebsiellapneumoniae 3(21.43%), Proteusvulgaris 1(7.14%) and Salmonellatyphi 1(7.14%). When screened for ESBL production based on CLSI breakpoint, only 6 (49.99%) were positive and included C.freundii 1(7.14%), E.coli 2(14.29%), K.pneumoniae 1(7.14%), S. typhi 1(7.14%) and 1(7.14%) for Ps. aeruginosa. On subjecting them to DDST, only 2(33.34%) out of them were found to be ESBLs positive by an increase in inhibition zone of 5mm toward the centre disc, Augmentin. They include E. coli 1(16.67%) and S. typhi 1(16.67%). Application: In a nutshell, foods and drinks sold therein could serve as reservoirs for ESBLs producing bacteria.

Keywords

ESBL, Foods and Drinks, Gombe Metropolis, Screening.
User

Abstract Views: 187

PDF Views: 0




  • Assessment of Foods and Drinks for the Presence of Extended Spectrum Beta Lactamase (ESBL) Producing Bacteria in Gombe Metropolis, Nigeria

Abstract Views: 187  |  PDF Views: 0

Authors

I. Shu’aibu
Department of Food Service and Management, Faculty of Food Science and Technology University Putra Malaysia,43400 Serdang, Selangor Darul Ehsan, Malaysia
J. A. Hadiza
Department of Microbiology, Gombe State University, P.M.B. 127, Gombe State, Nigeria
M. Yusha’u
Department of Microbiology, Bayero University Kano, P.M.B. 3011, Kano State, Nigeria
M. Y. Kabiru
College of Health sciences, Maryam Abacha American University of Niger, ADS Avenue, Roy Mohd VI, Du Maroc, Maradi, Republic Du Niger
M. M. Ahmad
Faculty of Chemical Engineering and Natural Resources, University Malaysia Pahang,26300 Gambang, Pahang, Malaysia
G. Lawal
Department of Microbiology, Gombe State University, P.M.B. 127, Gombe State, Nigeria
M. T. Adamu
Department of Microbiology, Gombe State University, P.M.B. 127, Gombe State, Nigeria
M. Khairiyya
Department of Microbiology, Gombe State University, P.M.B. 127, Gombe State, Nigeria

Abstract


Objectives: To make preliminary screening study for the presence of ESBL producing bacteria, in food and drinks sold in Gombe metropolis. 30 samples of food and drinks were collected and analyzed. Method: Bacterial isolation was performed on nutrient agar and identification started from gram staining; the gram negative isolates obtained, among which ESBL producers were found and further subjected to standard biochemical tests and confirmed to be enterobacteriaceae. They were then screened for ESBLs in accordance with Clinical and Laboratory Standard Institute (CLSI) breakpoint, and the suspected ESBLs bacteria were confirmed using double disc synergy testing (DDST) with standard Augmentin (Amoxycillin/ Clavulanic Acid, 30μg; Oxoid England, CT0223B), Ceftriaxone (CRO 30μg; Oxoid England, CT0417B) and Ceftazidime (CAZ 30μg; Oxoid England, CT0412B). Findings: The fourteen 14(100%) Gram negative bacteria isolated were found to include Pseudomonasaeruginosa 2(14.29%) and members of the family Enterobacteriaceae (enteric gram negative rods): Citrobacterfreundii 2(14.29%), Enterobacterspp. 1(7.14%), Escherichiacoli 4(28.57%), Klebsiellapneumoniae 3(21.43%), Proteusvulgaris 1(7.14%) and Salmonellatyphi 1(7.14%). When screened for ESBL production based on CLSI breakpoint, only 6 (49.99%) were positive and included C.freundii 1(7.14%), E.coli 2(14.29%), K.pneumoniae 1(7.14%), S. typhi 1(7.14%) and 1(7.14%) for Ps. aeruginosa. On subjecting them to DDST, only 2(33.34%) out of them were found to be ESBLs positive by an increase in inhibition zone of 5mm toward the centre disc, Augmentin. They include E. coli 1(16.67%) and S. typhi 1(16.67%). Application: In a nutshell, foods and drinks sold therein could serve as reservoirs for ESBLs producing bacteria.

Keywords


ESBL, Foods and Drinks, Gombe Metropolis, Screening.



DOI: https://doi.org/10.17485/ijst%2F2016%2Fv9i48%2F140852