Molecular Confirmation of the Causative Agents of Diarrhea and Its Antimicrobial Susceptibility Tests

Authors

  • Enerel Enkhbayar Department of Infectious Diseases, School of Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia https://orcid.org/0009-0006-9842-251X
  • Narangerel Baatar Infectious Diseases and Immunological laboratory, Institute of Veterinary Medicine, Ulaanbaatar, Mongolia
  • Avarzed Amgalanbaatar International Cyber Education Center, Graduate School, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia
  • Oyungerel Ravjir Department of Infectious Diseases, School of Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia

DOI:

https://doi.org/10.24079/cajms.2023.09.002

Keywords:

Foodborne Infection, Bloody Diarrhea, Salmonella, Shigella, Listeria

Abstract

Objectives: This study aimed to investigate molecular confirmation of the causative agents of diarrhea and its antimicrobial susceptibility tests in the samples collected from patients who have symptoms of diarrhea. There is a relative lack of diagnostic studies on the causative agents of diarrhea in Mongolia, especially on the causative agents of bacterial diarrhea and their antibiotic susceptibility. Methods: A rectal swab and stool sample were taken from 187 patients admitted to the NCCD Mongolia with a diagnosis of diarrhea and infection between June 2018 and April 2020 using a hospital-based instantaneous survey model, and bacteriology, molecular biology, and antibiotic susceptibility testing were performed at the laboratory of Bacteriology and Immunology, Institute of Veterinary Medicine. Results: Of the 187 samples, N=127 (67.9%), p<0.01) were confirmed by simple and multiplex PCR, and Salmonella spp., Shigella spp., E.Coli, and S.aureus were detected in n=20 (15.7%), n=16 (12.6%), n=20 (15.7%), and n=7 samples (5.5%), respectively. Multiplex PCR 3 samples did not detect the 16s rRNA gene of Campylobacteraceae and C.jejuni or cdt C gene of C.coli, all of which were negative. Therefore, multiplex PCR was performed for foursamples to detect pathogenic bacteria, and samples were E. coli positive but not campylobacter, salmonella, and shigella. Conclusion: 126 (67.4%) children aged 1-5 years were the most affected by foodborne infection, and most of the diarrhea causative agents detected were Salmonella spp, Shigella spp, E.Coli, and S.aureus. 

Abstract
34
PDF 76

References

Wolfsheim C, Fontaine O, Merson M. Evolution of the World Health Organization's programmatic actions to control diarrheal diseases. J Glob Health. 2019;9(2):020802. https://doi.org/10.7189/jogh.09.020802

Antonelli P, Belluco S, Mancin M, et al. Genes conferring resistance to critically important antimicrobials in Salmonella enterica isolated from animals and food: A systematic review of the literature 2013-2017. J Elsevier Res Vet Sci. 2019;126:59-67. https://doi.org/10.1016/j.rvsc.2019.08.022

Throckmorton L, Hancher J. Management of Travel-Related Infectious Diseases in the Emergency Department. Curr Emerg Hosp Med Rep. 2020;8(2):50-9. https://doi.org/10.1007/s40138-020-00213-6

Ali Saadi AB, Asmaa AH. Isolation and Identification of Escherichiacoli ProducingCytosine Deaminase from Iraqi patients. Int J Adv Res Biol. 2017;4(11):1-6. https://doi.org/10.22192/ijarbs.2017.04.11.001

Sergelidis D, Angelidis AS. Methicillin-resistant StaphylococcusAureus. Lett Appl Microbiol. 2017;64(6):409-18. https://doi.org/10.1111/lam.12735

Narantuya B, Gantsetseg Kh. Center for Health Development: Health Indicators 2019. Ulaanbaatar press; 2020:100-1.

Bor L. Report on antibiotic use and bacterial resistance. Ulaanbaatar Mongolia: Ulaanbaatar press; 2019:31-5.

Tsetsegmaa S, Erdenechimeg E. Surveillance of antibiotic use in Mongolia. Ulaanbaatar, Mongolia: Ulaanbaatar press; 2019:14-7.

Brown D, MacGowan A. Harmonization of antimicrobial susceptibility testing breakpoints in Europe: implications for reporting intermediate susceptibility. J Antimicrob Chemother. 2010;65:183-5. https://doi.org/10.1093/jac/dkp432

Kuijpers LMF, Post AS, Jacobs J. Chromogenic media for the detection of Salmonella Enterica serovar Paratyphi A in human stool samples: evaluation in reference setting. Eur J Clin Microbiol Infect Dis. 2018;37:11-10. https://doi.org/10.1007/s10096-018-3360-1

Wences A, Aron J, Olga H, et al. Incidence and etiology of infectious diarrhea from a facility–based surveillance system in Guatemala, 2008-2012. BMC Public Health. 2019; 19:1340. https://doi.org/10.1186/s12889-019-7720-2

Roya N, Ahmed S, Marjan D, et al. A study of the prevalence of Shigella species and antimicrobial resistance patterns in the pediatric medical center, Ahvaz, Iran. Iran J. Microbiol. 2017 Oct;9(5):277-83.

Elnaz A, Alireza A, Ehsanollah G. Frequency of Listeria monocytogenes Isolated from Diarrhea Samples of Pediatric Patients at Central Iran. Rep Biochem Mol Biol. 2019 Jul;8(2):172-7.

Nachamkin I, Nguyen P. Isolation of Campylobacter Species from Stool Samples by Use of a Filtration Method: Assessment from a United States-Based Population. J Clin Microbiol. 2017;55(7):2204-7. https://doi.org/10.1128/jcm.00332-17

Mihaiu L, Mihaiu M, Tabaran A, et al. Antimicrobial Resistance Evaluation of pathogen Salmonella strains isolated in pork and poultry meat 2013. Food and Agriculture Organization of the United Nations 2014;70:266-70. https://www.cabidigitallibrary.org/doi/pdf/10.5555/20143016564

Meiji S, Noriko U, Mitsuyo K, et al., eds. Molecular Epidemiological Characterization of Staphylococcus argenteus Clinical Isolates in Japan: Identification of Three Clones (ST1223, ST2198, and ST2550) and a Novel Staphylocoagulase Genotype XV 2019; 7(10): 389. https://doi.org/10.3390/microorganisms7100389

Bertrand P, Ceyssens J. Diversity of Listeria monocytogenes Strains of Clinical and Food Chain Origins in Belgium between 1985 and 2014. PLoS One. 2016; Release of WHO News 2017. https://doi.org/10.1371/journal.pone.0164283

World Health Organization (WHO). WHO’s first-ever global estimates of foodborne diseases find children under 5 account for almost one-third of deaths Dec 2015. WHO; 2015.

Olivier D, Alexandra M, Marc L. Making Sense of the Biodiversity and Virulence of Listeria monocytogenes. Trends Microbiol. 2021;29(9):811-22. https://doi.org/10.1016/j.tim.2021.01.008

Baserisalehi M, Al-Mahdi AY, Kapadnis BP. Antimicrobial susceptibility of thermophilic Campylobacter spp. Isolated from environmental samples. Indian J Med Microbiol. 2005;23(1):48-51. https://doi.org/10.4103/0255-0857.13874

Razei A, Sorouri R, Mousavi Se, al., eds, Presenting a rapid method for detection of Bacillus cereus, Listeria monocytogenes and Campylobacter jejuni in food samples. Iran J Basic Med Sci. 2017;20(9):1050-5. https://doi.org/10.22038/IJBMS.2017.9275

Best EL, Powel EJ, Swift C, et al. eds. Applicability of a rapid duplex real-time PCR assay for speciation of Campylobacter jejuni and Campylobacter coli directly from culture plates. FEMS Microbiology 2003;19:169-71. https://doi.org/10.1016/s0378-1097(03)00845-0

Soomin L, Jeeyeon L, Jimyeong H, et al. eds. Clinical relevance of infections with zoonotic and human oral species of Campylobacter. J. Microbiology 2016;54(7):459-67. https://doi.org/10.1007/s12275-016-6254-x

Hugho EA, Kumburu HH, Amani NB, et al. eds. Enteric Pathogens Detected in Children under Five Years Old Admitted with Diarrhea in Moshi, Kilimanjaro, Tanzania. Pathogens. 2023;12(4):618. https://doi.org/10.3390/pathogens12040618

Downloads

Published

2023-09-30

How to Cite

Enkhbayar, E., Baatar, N., Amgalanbaatar, A., & Ravjir, O. (2023). Molecular Confirmation of the Causative Agents of Diarrhea and Its Antimicrobial Susceptibility Tests. Central Asian Journal of Medical Sciences, 9(3), 117–124. https://doi.org/10.24079/cajms.2023.09.002

Issue

Section

Articles