Isolation and characterization of staphylococcus aureus from two large-scale food poisoning outbreaks in Vietnam

View or download the full article: 
UDC: 
61; 613.2; 614; 615
Authors: 

Lam Quoc Hung1, Huong Minh Nguyen3, Ta Thi Yen2, Le Vinh Hoa2, Tran Hong Ba2, Pham Le Quyen2,4, Do Thi Thu Huong5, Nguyen Thanh Trung2, Le Thi Hong Hao2

Organization: 

1Vietnam Food Administration, 1135 Pho Nui Truc, Giang Vo, Ba Dinh, Hanoi, Vietnam
2National Institute for food control, NIFC-Vietnam, 65 Pham Than Duat, Hanoi, Vietnam
3Institute of Biotechnology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, CauGiay, Hanoi, Vietnam
4Quang Binh Center for Disease Control and Prevention, 3150 Rampart Road, Fort Collins, USA
5National Agro-Forestry Fisheries Quality Assurance Department, 10 Nguyen Kong Hoan, Ba Đình, Hanoi, Vietnam

Abstract: 

In Vietnam and around the world, Staphylococcus aureus remains a major hazard of food safety and food poisoning. S. aureus is present in many places and easily contaminates food production during processing chains.
In this study, we successfully isolated S. aureus strains from suspected samples of two food borne poisoning outbreaks in Ha Giang and Vinh Phuc in 2017 and 2018, respectively. The collected samples were examined for presence of staphylococcal enterotoxins (SEs) by using 3MTMTECRATM Staph Enterotoxin kit, from there all the samples were positive with SEs. Different strains of S. aureus were isolated and then confirmed by MALDI-TOF technique. Those strains then were stored in Brain heart solution with 15% glycerol until further analysis.
Our results identified three STs, ST96, ST88 (spa type t7558), and ST72 (spa type t3092), were responsible for two outbreaks. Two virulence genes detected from the above strains were sea and sec. Furthermore, these strains are test for antibiotic resistance susceptibility with commonly antibiotics. Penicillin are found to be resisted by all three STs, in particularly, ST96 and ST88 are both resistant to erythromycin while ST72 is resistant to gentamicin.
Taken together, our study highlights the usefulness of molecular characterization to study and monitor bacterial pathogens associated with food poisoning outbreaks in Vietnam.

Keywords: 
antibiotic-resistant, food poisoning, β-lactamase, ESBL, ampC β-lactamases, Staphylococcus areus, MLST, Spa genes, staphylococcal toxins.
Lam Quoc Hung, Huong Minh Nguyen, Ta Thi Yen, Le Vinh Hoa, Tran Hong Ba, Pham Le Quyen, Do Thi Thu Huong, Nguyen Thanh Trung, Le Thi Hong Hao. Isolation and characterization of staphylococcus aureus from two large-scale food poisoning outbreaks in Vietnam. Health Risk Analysis, 2020, no. 3, pp. 139–147. DOI: 10.21668/health.risk/2020.3.17.eng
References: 
  1. Kadariya J., Smith T.C., Thapaliya D. Staphylococcus aureus and Staphylococcal Food-Borne Disease: An Ongoing Challenge in Public Health. BioMed Research International, 2014, vol. 214, no. 1, pp. 827965. DOI: 10.1155/2014/82796
  2. The European Union Summary Report on Trends and Sources of Zoonoses, Zoonotic Agents and Food-borne Outbreaks in 2010. EFSA Journal, 2012, vol. 10, no. 3, pp. 2597. DOI: 10.2903/j.efsa.2012.2597
  3. The European Union Summary Report on Trends and Sources of Zoonoses, Zoonotic Agents and Food-borne Outbreaks in 2011. EFSA Journal, 2013, vol. 11, no. 4, pp. 3129. DOI: 10.2903/j.efsa.2013.3129
  4. Joint Annual Health Review 2015. Hanoi, Vietnam Ministry of health, Medical publishing house Publ., 2016, 223 p.
  5. Sub Department of Food Hygiene and Safety of Ho Chi Minh. School food safety assurance report, 2016, 103 p.
  6. Bhunia A. Foodborne Microbial Pathogens. New York, Springer-Verlag Publ., 2019, 273 p.
  7. Microbiology of food and animal feeding stuffs – Horizontal methods for sampling techniques from surfaces using contact plates and swabs. Vietnamese Ministry of Science and Technology, 2009. Available at: https://vanbanphapluat.co/tcvn-8129-2009-vi-sinh-vat-trong-thuc-pham-va-... (10.04.2020).
  8. Pinchuk I.V., Beswick E.J., Reyes V.E. Staphylococcal Enterotoxins. Toxins, 2010, vol. 2, no. 8, pp. 2177–2197. DOI: 10.3390/toxins2082177
  9. Bad bug book: handbook of foodborne pathogenic microorganisms and natural toxins. Second Edition. Hanoi, Food and Drug Administration Publ., 2012, 292 p.
  10. Chaibenjawong P., Foster S.J. Desiccation tolerance in Staphylococcus aureus. Archives of Microbiology, 2010, vol. 193, no. 2, pp. 125–135. DOI: 10.1007/s00203-010-0653-x
  11. Argudín M.Á., Mendoza M.C., Rodicio M.R. Food Poisoning and Staphylococcus aureus Enterotoxins. Toxins, 2010, vol. 2, no. 7, pp. 1751–1773. DOI: 10.3390/toxins2071751
  12. Koreen L., Ramaswamy S.V., Graviss E.A., Naidich S., Musser J.M., Kreiswirth B.N. spa Typing Method for Discriminating among Staphylococcus aureus Isolates: Implications for Use of a Single Marker To Detect Genetic Micro- and Macrovariation. Journal of Clinical Microbiology, 2004, vol. 42, no. 2, pp. 792–799. DOI: 10.1128/jcm.42.2.792-799.2004
  13. Official Methods of Analysis of AOAC International. 19-th edition. Gaithersburg, AOAC International Publ., 2012, 771 p.
  14. Performance standards for antimicrobial susceptibility testing. 29-th edition. Clinical and Laboratory Standards Institute (CLSI) Publ., 2016, 25 p.
  15. Magiorakos A., Srinivasan A., Carey R., Carmeli Y., Falagas M., Giske C., Harbarth S., Hindler J. [et al.]. Multidrugresistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clinical Microbiology and Infection, 2012, vol. 18, no. 3, pp. 268–281. DOI: 10.1111/j.1469-0691.2011.03570.x
  16. Johnson W.M., Tyler S.D., Ewan E.P., Ashton F.E., Pollard D.R., Rozee K.R. Detection of genes for enterotoxins, exfoliative toxins, and toxic shock syndrome toxin 1 in Staphylococcus aureus by the polymerase chain reaction. Journal of Clinical Microbiology, 1991, vol. 24, pp. 426–430. DOI: 10.1128/JCM.29.3.426-430.1991
  17. Jolley K., Bray J. Maiden M. Open-access bacterial population genomics: BIGSdb software, the PubMLST.org website and their applications. Wellcome Open Research, 2018, vol. 3, pp. 124. DOI: 10.12688/wellcomeopenres.14826.1
  18. Strommenger B., Kettlitz C., Weniger T., Harmsen D., Friedrich A.W., Witte W. Assignment of Staphylococcus Isolates to Groups by spa Typing, SmaI Macrorestriction Analysis, and Multilocus Sequence Typing. Journal of Clinical Microbiology, 2006, vol. 44, no. 7, pp. 2533–2540. DOI: 10.1128/jcm.00420-06
  19. Feil E.J., Li B.C., Aanensen D.M., Hanage W.P., Spratt B.G. eBURST: Inferring Patterns of Evolutionary Descent among Clusters of Related Bacterial Genotypes from Multilocus Sequence Typing Data. Journal of Bacteriology, 2004, vol. 186, no. 5, pp. 1518–1530. DOI: 10.1128/jb.186.5.1518-1530.2004
  20. Argimón S., Abudahab K., Goater R., Fedosejev A., Bhai J., Glasner C., Feil E., Holden M. [et al.]. Microreact: visualizing and sharing data for genomic epidemiology and phylogeography. Microbial Genomics, 2016, vol. 2, no. 11, pp. 1–11. DOI: 10.1099/mgen.0.000093
  21. Mellmann A., Weniger T., Berssenbrügge C., Rothgänger J., Sammeth M., Stoye J., Harmsen D. Based Upon Repeat Pattern (BURP): an algorithm to characterize the long-term evolution of Staphylococcus aureus populations based on spa polymorphisms. BMC Microbiology, 2007, vol. 7, article number 98. DOI: 10.1186/1471-2180-7-98
  22. Mapping of spa with MLST S. aureus database. Ridom SpaServer, 2020. Available at: http://spa.ridom.de/mlst.shtml (19.03.2020).
  23. The community summary report on trends and sources of zoonoses and zoonotic agents and food-borne outbreaks in the European Union in 2008. EFSA Journal, 2010, vol. 8, no. 1, pp. 1496. DOI: 10.2903/j.efsa.2010.1496
Received: 
14.04.2020
Accepted: 
17.08.2020
Published: 
30.09.2020

You are here