Multidisciplinary research and review journal | Online ISSN 3064-9870
RESEARCH ARTICLE   (Open Access)

Antibiotic Sensitivity Pattern of Staphylococcus aureus Isolated from Various Dry Foods

Golam Md. Sarwar 1, Maruf Abony 2, Suvamoy Datta 2*

+ Author Affiliations

Journal of Primeasia 2(1) 1-6 https://doi.org/10.25163/primeasia.2120213

Submitted: 19 January 2021  Revised: 18 March 2021  Published: 22 March 2021 

Abstract

Background: Staphylococcus aureus is a well-known pathogen responsible for a range of clinical and localized infections, including nosocomial methicillin-resistant S. aureus (MRSA) infections. The emergence of vancomycin-resistant S. aureus (VRSA) strains has further complicated treatment options. Globally, food-borne diseases (FBD), including those caused by S. aureus, pose significant public health concerns. This study investigates the prevalence and antibiotic resistance of S. aureus in ready-to-eat packaged foods in Dhaka, Bangladesh, to better understand food safety risks. Methods: Samples of ready-to-eat packaged foods were collected from superstores in Dhaka and transported to the laboratory under appropriate conditions. Bacterial isolation was performed using standard methods on Mannitol salt agar medium, followed by incubation at 37°C for 24 hours. Biochemical tests, including the Catalase Test, IMViC tests, and Coagulase Test, were conducted for bacterial identification. Antibiotic susceptibility testing was performed using the Kirby-Bauer method with a range of antibiotics including amoxicillin, gentamicin, penicillin, chloramphenicol, ciprofloxacin, ceftriaxone, cephradine, nalidixic acid, erythromycin, and azithromycin. Results: The study found that resistance among S. aureus strains varied significantly, from 0% for gentamicin to 100% for amoxicillin. Gentamicin was the most effective antibiotic, with 100% sensitivity, followed by chloramphenicol with 95% sensitivity. Of the samples, 2.5% showed resistance to six antibiotics, 12.5% were resistant to at least five antibiotics, and overall, 27.5% of the strains were multidrug-resistant. These results align with findings from similar studies conducted in China and Greece. Conclusion: The study highlights the significant presence of multidrug-resistant S. aureus in ready-to-eat packaged foods in Dhaka. Preventing staphylococcal food poisoning requires strict adherence to hygiene practices, proper food storage, and thorough cooking. Education of food handlers on Good Manufacturing Practices (GMP) and Good Hygienic Practices (GHP) is essential to reduce contamination risks. Further research on the impact of hygiene on the development of food-borne illnesses is recommended to enhance food safety measures.

Keywords: Staphylococcus aureus, food-borne, multidrug resistance, antibiotic susceptibility, packaged food. 

References

Abebe, M., Daniel, A., Yimtubezinash, W., & Genene, T. (2013). Identification and antimicrobial susceptibility of Staphylococcus aureus isolated from milk samples of dairy cows and nasal swabs of farm workers in selected dairy farms around Addis Ababa, Ethiopia. African Journal of Microbiology Research, 7(27), 3501-3510.

Abony, M., Banik, A., Muhaiminul, K., Jannat, B., & Datta, S. (2018). Isolation and identification of antibiotic-producing microorganism from Actinomycetaceae family from soil samples of Dhaka and Comilla. Journal of Primeasia University, 2(1), 11-18.

Addo, K. K., Mensah, G. I., Aning, K. G., Nartey, N., Nipah, G. K., Bonsu, C., Akyeh, M. L., & Smits, H. L. (2011). Microbiological quality and antibiotic residues in informally marketed raw cow milk within the coastal savannah zone of Ghana. Tropical Medicine & International Health, 16(2), 227-232.

Adesiji, Y. O., Alli, O. T., Adekanle, M. A., & Jolayemi, J. B. (2011). Prevalence of Arcobacter, Escherichia coli, Staphylococcus aureus, and Salmonella species in retail raw chicken, pork, beef, and goat meat in Osogbo, Nigeria. Journal of Biomedical Research, 3(1), 8-12.

Ahmadi, M., Rohani, S. M. R., & Ayremlou, N. (2009). Detection of Staphylococcus aureus in milk by PCR. Comparative Clinical Pathology, 19(1), 91-94.

Akhi, M. A., Das, N. C., Banik, A., Abony, M., Juthi, M., & Uddin, M. E. (2019). Detection of drug-resistant S. aureus from poultry samples collected from different areas of Bangladesh. Microbiology Research Journal International, 29(1), 1-10.

Akhi, M., Banik, A., Ghurnee, O., Das, N., Nondi, S., & Abony, M. (2019). Prevalence and antibiogram profiling of rotten fruits from different areas of Dhaka City, Bangladesh. European Journal of Medicinal Plants, 1-9.

Ateba, C. N., Mbewe, M., Moneoang, M. S., & Bezuidenhout, C. C. (2010). Antibiotic-resistant Staphylococcus aureus isolated from milk in the Mafikeng Area, North West province. South African Journal of Science, 106(1-2), 1-6.

Aydin, A., Sudagidan, M., & Muratoglu, K. (2011). Prevalence of staphylococcal enterotoxins, toxin genes, and genetic relatedness of foodborne Staphylococcus aureus strains isolated in the Marmara Region of Turkey. International Journal of Food Microbiology, 148(2), 99-106.

Beyene, G. F. (2016). Antimicrobial susceptibility of Staphylococcus aureus in cow milk, Afar Ethiopia. International Journal of Modern Chemistry and Applied Science, 3(1), 280-283.

Bryant, C. (2017). Investment opportunities in Mekelle, Tigray state, Ethiopia. Retrieved from https://www.ciaonet.org/attachments/15494

Clinical and Laboratory Standards Institute (CLSI). (2008). Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals (3rd ed., Approved standard M31-A3). Wayne, PA: CLSI.

Clinical and Laboratory Standards Institute (CLSI). (2012). Performance standards for antimicrobial susceptibility testing; Twenty-second informational supplement (CLSI document M100-S22). Wayne, PA: CLSI.

Cohen, M. L. (2000). Changing patterns of infectious disease. Nature, 406(6797), 762-767.

Cong, Y., Yang, S., & Rao, X. (2020). Vancomycin-resistant Staphylococcus aureus infections: A review of case updating and clinical features. Journal of Advanced Research, 21, 169-176.

Ekici, K., Bozkurt, H., & Isleyici, O. (2004). Isolation of some pathogens from raw milk of different milk animals. Pakistan Journal of Nutrition, 3(3), 161-162.

El-Gedawy, A. A., Ahmed, H. A., & Awadallah, M. A. (2014). Occurrence and molecular characterization of some zoonotic bacteria in bovine milk, milking equipment, and humans in dairy farms, Sharkia, Egypt. International Food Research Journal, 21(5), 1813-1823.

Gooraninejad, S., Ghorbanpoor, M., & Salati, A. P. (2007). Antibiotic susceptibility of staphylococci isolated from bovine sub-clinical mastitis. Pakistan Journal of Biological Sciences, 10(16), 2781-2783.

Hamid, S., Bhat, M. A., Mir, I. A., Taku, A., Badroo, G. A., Nazki, S., & Malik, A. (2017). Phenotypic and genotypic characterization of methicillin-resistant Staphylococcus aureus from bovine mastitis. Veterinary World, 10(3), 363-367.

Hassoun, A., Linden, P. K., & Friedman, B. (2017). Incidence, prevalence, and management of MRSA bacteremia across patient populations—a review of recent developments in MRSA management and treatment. Critical Care, 21(1), 1-10.

Hennekinne, J.-A., De Buyser, M.-L., & Dragacci, S. (2012). Staphylococcus aureus and its food poisoning toxins: Characterization and outbreak investigation. FEMS Microbiology Reviews, 36(4), 815-836.

Kadariya, J., Smith, T. C., & Thapaliya, D. (2014). Staphylococcus aureus and staphylococcal food-borne disease: An ongoing challenge in public health. BioMed Research International, 2014, 1-10.

Le Loir, Y., Baron, F., & Gautier, M. (2003). Staphylococcus aureus and food poisoning. Genetics and Molecular Research, 2(1), 63-76.

Md. Eaktear Uddin, Shakila Sultana, Maruf Abony et al., (2020). Antibiotic Sensitivity Pattern of Staphylococcus aureus Isolated from Pus Samples of Different Age and Sex Groups in Gazipur District, Bangladesh, Journal of Primesia University, 1(1), 1-8, 560013

Scallan, E., Jones, T. F., Cronquist, A., Thomas, S., Frenzen, P., Hoefer, D., et al. (2006). Factors associated with seeking medical care and submitting a stool sample in estimating the burden of foodborne illness. Foodborne Pathogens & Disease, 3(4), 432-438.

Sergelidis, D., Abrahim, A., Anagnostou, V., Govaris, A., Papadopoulos, T., & Papa, A. (2012). Prevalence, distribution, and antimicrobial susceptibility of Staphylococcus aureus in ready-to-eat salads and in the environment of a salad manufacturing plant in Northern Greece. Czech Journal of Food Sciences, 30(3), 285-291.

Shariati, A., Dadashi, M., Moghadam, M. T., van Belkum, A., Yaslianifard, S., & Darban-Sarokhalil, D. (2020). Global prevalence and distribution of vancomycin-resistant, vancomycin-intermediate, and heterogeneously vancomycin-intermediate Staphylococcus aureus clinical isolates: A systematic review and meta-analysis. Scientific Reports, 10(1), 1-16.

Sofos, J. N. (2008). Challenges to meat safety in the 21st century. Meat Science, 78(1-2), 3-13.

Syne, S.-M., Ramsubhag, A., & Adesiyun, A. A. (2013). Microbiological hazard analysis of ready-to-eat meats processed at a food plant in Trinidad, West Indies. Infection Ecology & Epidemiology, 3(1), 20450.

Tiwari, H. K., & Sen, M. R. (2006). Emergence of vancomycin-resistant Staphylococcus aureus (VRSA) from a tertiary care hospital from northern part of India. BMC Infectious Diseases, 6(1), 1-6.

Tong, S. Y., Davis, J. S., Eichenberger, E., Holland, T. L., & Fowler Jr, V. G. (2015). Staphylococcus aureus infections: Epidemiology, pathophysiology, clinical manifestations, and management. Clinical Microbiology Reviews, 28(3), 603-661.

Yang, X., Zhang, J., Yu, S., Wu, Q., Guo, W., Huang, J., et al. (2016). Prevalence of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus in retail ready-to-eat foods in China. Frontiers in Microbiology, 7, 816.

PDF
Full Text
Export Citation

View Dimensions


View Plumx



View Altmetric



1
Save
0
Citation
275
View
0
Share