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Prevalence of multidrug resistance Salmonella species isolated from clinical specimens at University of Gondar comprehensive specialized hospital Northwest Ethiopia: A retrospective study.

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  • معلومة اضافية
    • المصدر:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
    • بيانات النشر:
      Original Publication: San Francisco, CA : Public Library of Science
    • الموضوع:
    • نبذة مختصرة :
      Background: Multidrug resistance Salmonellosis remains an important public health problem globally. The disease is among the leading causes of morbidity and mortality in developing countries, but there have been limited recent studies about the prevalence, antimicrobial resistance, and multidrug resistance patterns of Salmonella isolates from various clinical specimens.
      Objective: Aimed to assess the prevalence, antimicrobial resistance, and multidrug resistance patterns of Salmonella isolates from clinical specimens at the University of Gondar Comprehensive Specialised Hospital, northwestern Ethiopia.
      Method: A retrospective hospital-based cross-sectional study was conducted to determine the prevalence, antimicrobial resistance, and multidrug resistance patterns of isolated from all clinical specimens at the University of Gondar Salmonella Comprehensive Specialised Hospital from June 1st, 2017 to June 3rd, 2022. A total of 26,154 data points were collected using a checklist of records of laboratory registration. Clinical specimens were collected, inoculated, and incubated for about a week with visual inspection for growth and gram staining. The isolates were grown on MacConkey agar and Xylose Lysine Deoxycholate agar. Pure colonies were identified with a conventional biochemical test, and those unidentified at the species level were further identified by the analytical profile index-20E. Then, antimicrobial susceptibility was determined by the Kirby-Bauer disc diffusion technique. The multidrug resistance Salmonella isolates was identified using the criteria set by Magiorakos. Finally, the data was cleaned and checked for completeness and then entered into SPSS version 26 for analysis. Then the results were displayed using tables and figures.
      Results: Of the total 26,154 Salmonella suspected clinical samples, 41 (0.16%) Salmonella species were isolated. Most of the Salmonella isolates, 19 (46.3%), were in the age group of less than 18 years, followed by the age group of 19-44 years, 11 (26.8%). In this study, S. enterica subsp. arizonae accounts for the highest 21 (51%), followed by S. paratyphi A 9 (22%). Of the Salmonella isolates, S. typhi were highly resistant to ampicillin (100%), followed by tetracycline and trimethoprim-sulfamethoxazole, each accounting for 83.3%. Furthermore, S. paratyphi A was resistant to ampicillin (100%), tetracycline (88.9%), and chloramphenicol (88.9%). The overall multi-drug resistance prevalence was 22 (53.7%; 95% CI: 39.7-61). Accordingly, S. paratyphi A was 100% multidrug-resistant, followed by S. typhi (66.6%).
      Conclusion: A low prevalence of Salmonella species was observed in the past six years. Moreover, most S. typhi and S. paratyphi strains in the study area were found to be resistant to routinely recommended antibiotics like ciprofloxacin and ceftriaxone, compared to what was reported earlier. In addition, all isolates of S. paratyphi A and the majority of S. typhi were multidrug resistant. Therefore, health professionals should consider antimicrobial susceptibility tests and use antibiotics with caution for Salmonellosis management.
      Competing Interests: The authors have declared that no competing interests exist
      (Copyright: © 2024 Amare et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
    • References:
      Environ Health Prev Med. 2018 Oct 27;23(1):54. (PMID: 30368236)
      Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S317-24. (PMID: 26449947)
      Int J Infect Dis. 2015 Jun;35:96-102. (PMID: 25931197)
      J Infect Dev Ctries. 2020 Feb 29;14(2):169-176. (PMID: 32146451)
      J Infect Dev Ctries. 2011 Feb 01;5(1):23-33. (PMID: 21330737)
      Genome Announc. 2014 Oct 30;2(5):. (PMID: 25359907)
      Afr J Lab Med. 2018 Dec 06;7(2):770. (PMID: 30568898)
      Food Microbiol. 2018 May;71:55-59. (PMID: 29366469)
      Ann Clin Microbiol Antimicrob. 2018 Feb 1;17(1):1. (PMID: 29391040)
      Microorganisms. 2021 Nov 30;9(12):. (PMID: 34946085)
      Microbiology (Reading). 2018 Nov;164(11):1327-1344. (PMID: 30136920)
      Foodborne Pathog Dis. 2011 Jun;8(6):693-7. (PMID: 21388293)
      Sci Rep. 2021 Apr 1;11(1):7359. (PMID: 33795754)
      Infect Drug Resist. 2021 Nov 25;14:4957-4966. (PMID: 34858036)
      Clin Infect Dis. 2010 Jan 15;50(2):241-6. (PMID: 20014951)
      SAGE Open Med. 2021 Apr 16;9:20503121211009729. (PMID: 33948178)
      SAGE Open Med. 2019 Mar 15;7:2050312119837854. (PMID: 30906553)
      J Pathog. 2016;2016:4065603. (PMID: 26942013)
      ScientificWorldJournal. 2015;2015:520179. (PMID: 25664339)
      PLoS One. 2022 Mar 17;17(3):e0264818. (PMID: 35298493)
      Int J Infect Dis. 2010 Sep;14 Suppl 3:e93-9. (PMID: 20236850)
      Foodborne Pathog Dis. 2021 Nov;18(11):778-783. (PMID: 34197185)
      Infect Drug Resist. 2017 Jan 13;10:19-25. (PMID: 28144154)
      Oman Med J. 2019 May;34(3):184-193. (PMID: 31110624)
      Trop Dis Travel Med Vaccines. 2020 Sep 11;6:19. (PMID: 32944267)
      Front Microbiol. 2015 Jan 21;5:791. (PMID: 25653644)
      Clin Microbiol Infect. 2012 Mar;18(3):268-81. (PMID: 21793988)
      Int J Microbiol. 2019 Aug 01;2019:2489063. (PMID: 31467550)
      J Clin Microbiol. 2020 Feb 24;58(3):. (PMID: 31915289)
      BMC Med. 2020 Mar 13;18(1):49. (PMID: 32164681)
      Microbiol Res. 2018 Jan;206:60-73. (PMID: 29146261)
      BMC Res Notes. 2014 Aug 18;7:545. (PMID: 25134959)
      Lancet Infect Dis. 2013 Aug;13(8):672-9. (PMID: 23721756)
      BMC Infect Dis. 2021 Jan 7;21(1):30. (PMID: 33413186)
      Yale J Biol Med. 2017 Jun 23;90(2):283-290. (PMID: 28656014)
      PLoS One. 2021 Dec 2;16(12):e0256556. (PMID: 34855767)
      BMC Pharmacol Toxicol. 2014 May 19;15:26. (PMID: 24887310)
      Trans R Soc Trop Med Hyg. 2015 Aug;109(8):538-40. (PMID: 25979527)
      Clin Infect Dis. 2010 Mar 15;50(6):882-9. (PMID: 20158401)
      Trends Microbiol. 2014 Nov;22(11):648-55. (PMID: 25065707)
      Malawi Med J. 2019 Sep;31(3):184-192. (PMID: 31839887)
      Infect Drug Resist. 2020 Nov 04;13:3991-4002. (PMID: 33177849)
      J Infect Dis. 2018 Nov 10;218(suppl_4):S206-S213. (PMID: 30307566)
      East Afr Med J. 2014 Mar;91(3):73-6. (PMID: 26859034)
      PLoS Negl Trop Dis. 2018 Jun 8;12(6):e0006571. (PMID: 29883448)
      Infect Dis Rep. 2021 Apr 21;13(2):388-400. (PMID: 33919283)
      BMC Res Notes. 2014 Sep 17;7:653. (PMID: 25231649)
      Biomed Res Int. 2018 May 23;2018:6406405. (PMID: 29951540)
      Nat Commun. 2021 Aug 9;12(1):4786. (PMID: 34373455)
      SAGE Open Med. 2019 May 10;7:2050312119846041. (PMID: 31205690)
      Nepal Med Coll J. 2011 Jun;13(2):69-73. (PMID: 22364084)
      Asian Pac J Trop Biomed. 2014 Apr;4(4):306-11. (PMID: 25182556)
    • الرقم المعرف:
      0 (Anti-Bacterial Agents)
    • الموضوع:
      Date Created: 20240507 Date Completed: 20240507 Latest Revision: 20240509
    • الموضوع:
      20240509
    • الرقم المعرف:
      PMC11075907
    • الرقم المعرف:
      10.1371/journal.pone.0301697
    • الرقم المعرف:
      38713729