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Journal of the South African Veterinary Association2018; 89; e1-e10; doi: 10.4102/jsava.v89i0.1643

Detection of Salmonella from animal sources in South Africa between 2007 and 2014.

Abstract: Retrospective laboratory-based surveillance was conducted on Salmonella serotypes isolated from various animal species from 2007 to 2014 at the Agricultural Research Council, Onderstepoort Veterinary Research Institute, South Africa. During the surveillance period, 1229 salmonellae isolations were recorded. Around 108 different serotypes were recovered from nine different food and non-food animal host species. The three most common serotypes were Salmonella entericasubspecies enterica serotype Heidelberg (n = 200), Salmonella enterica subspecies enterica serotype Enteritidis (n = 170) and Salmonella enterica subspecies enterica serotype Typhimurium (n = 146). These were followed by Salmonella enterica subspecies enterica serotype Anatum (n = 62) and Salmonella entericasubspecies enterica serotype Infantis (n = 57). Salmonella enterica subspecies enterica serotype Schwarzengrund and Salmonella enterica subspecies entericaserotype Muenchen were recovered in 50 and 48 cases, respectively. Of the total number of isolations recorded during the period under review, 871 (70.8%) occurred in poultry and other birds, 162 (13.2%) in horses, 116 (9.4%) in cattle, 26 (2.1%) in sheep and goats, 22 (1.8%) in rhinoceroses, 16 (1.3%) in pigs, 8 (0.6%) in crocodiles, 6 (0.5%) in cats and 6 (0.5%) in leopards. Food animals accounted for 83.5% of the total isolations, with cattle and poultry representing approximately 72.7%. Forty-two (3.4 %) isolates were found from non-food animals that include rhinoceroses (n = 22), crocodiles (n = 8), leopards (n = 6) and cats (n = 6). Salmonella Heidelberg was the most frequently isolated serotype, whereas S. Typhimurium had the widest zoological distribution. Clinical laboratory isolation of different Salmonella serotypes from various hosts may aid in recognising the threat to livestock, public and environmental health. Moreover, it may also highlight the potential zoonotic and food safety risk implications of the detected Salmonella serotypes.
Publication Date: 2018-11-07 PubMed ID: 30456978PubMed Central: PMC6244140DOI: 10.4102/jsava.v89i0.1643Google Scholar: Lookup
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  • Journal Article

Summary

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This research involved a retrospective study on different types of Salmonella (referred to as serotypes) isolated from different species of animals in South Africa between 2007 and 2014. The study found a wide distribution of various Salmonella serotypes in different host species, highlighting potential health risks to both humans and animals.

Scope of the Research

  • The study was a retrospective laboratory-based surveillance carried out on Salmonella serotypes isolated from various animal species over a period of seven years.
  • The analysis was performed at the Agricultural Research Council, Onderstepoort Veterinary Research Institute in South Africa.
  • Out of nine different host species, 108 different serotypes of Salmonella were isolated.

Major Findings

  • The surveillance period recorded a total of 1229 Salmonella isolations.
  • The three most common Salmonella serotypes found were Salmonella enterica serotype Heidelberg, Salmonella enterica serotype Enteritidis, and Salmonella enterica serotype Typhimurium. These were followed by Salmonella enterica serotype Anatum and Salmonella enterica serotype Infantis.
  • By host species, the highest number of isolations recorded occurred in poultry and other birds. This was followed by horses, cattle, sheep and goats, rhinoceroses, pigs, crocodiles, cats, and leopards.

Health Implications

  • Food animals accounted for 83.5% of the total isolations, inevitably bringing potential food safety risks into light.
  • Non-food animals including rhinoceroses, crocodiles, leopards, and cats also hosted a small percentage of isolations. These findings indicate potential zoonotic risks.
  • Given the wide zoological distribution of Salmonella, the study highlights the urgency to be vigilant over the public, environmental, and animal health threats posed by the bacteria.

Concluding Remarks

  • The research underscores the importance of continuous surveillance of Salmonella serotypes in various hosts which can serve as an early warning and preventive measure against potential health crises.
  • The findings also highlight food and zoonotic safety risks, drawing decision makers’ attention towards implementing strategies to mitigate these potential threats.

Cite This Article

APA
Gelaw AK, Nthaba P, Matle I. (2018). Detection of Salmonella from animal sources in South Africa between 2007 and 2014. J S Afr Vet Assoc, 89, e1-e10. https://doi.org/10.4102/jsava.v89i0.1643

Publication

ISSN: 2224-9435
NlmUniqueID: 7503122
Country: South Africa
Language: English
Volume: 89
Pages: e1-e10
PII: 1643

Researcher Affiliations

Gelaw, Awoke K
  • Agricultural Research Council, Irene. kidanemariama@arc.agric.za.
Nthaba, Palesa
    Matle, Itumeleng

      MeSH Terms

      • Animals
      • Food Microbiology
      • Population Surveillance / methods
      • Retrospective Studies
      • Salmonella / classification
      • Salmonella / isolation & purification
      • Salmonella Infections, Animal / diagnosis
      • Salmonella Infections, Animal / epidemiology
      • Salmonella Infections, Animal / microbiology
      • Serogroup
      • South Africa / epidemiology

      Conflict of Interest Statement

      The authors declare that there is no conflict of interest with regard to the writing of this article.

      References

      This article includes 36 references
      1. Altekruse SF, Bauer N, Chanlongbutra A, DeSagun R, Naugle A, Schlosser W, Umholtz R, White P. Salmonella enteritidis in broiler chickens, United States, 2000-2005.. Emerg Infect Dis 2006 Dec;12(12):1848-52.
        doi: 10.3201/eid1212.060653pmc: PMC3291361pubmed: 17326935google scholar: lookup
      2. Altekruse S, Koehler J, Hickman-Brenner F, Tauxe RV, Ferris K. A comparison of Salmonella enteritidis phage types from egg-associated outbreaks and implicated laying flocks.. Epidemiol Infect 1993 Feb;110(1):17-22.
        doi: 10.1017/S0950268800050639pmc: PMC2271964pubmed: 8432319google scholar: lookup
      3. Amavisit P, Markham PF, Lightfoot D, Whithear KG, Browning GF. Molecular epidemiology of Salmonella Heidelberg in an equine hospital.. Vet Microbiol 2001 May 3;80(1):85-98.
        pubmed: 11278126doi: 10.1016/s0378-1135(00)00373-4google scholar: lookup
      4. Anderson RJ, Walker RL, Hird DW, Blanchard PC. Case-control study of an outbreak of clinical disease attributable to Salmonella menhaden infection in eight dairy herds.. J Am Vet Med Assoc 1997 Feb 15;210(4):528-30.
        doi: 10.1016/S0378-1135(00)00373-4pubmed: 9040841google scholar: lookup
      5. Bahnson PB, Fedorka-Cray PJ, Ladely SR, Mateus-Pinilla NE. Herd-level risk factors for Salmonella enterica subsp. enterica in U.S. market pigs.. Prev Vet Med 2006 Oct 17;76(3-4):249-62.
      6. Bäumler AJ, Tsolis RM, Ficht TA, Adams LG. Evolution of host adaptation in Salmonella enterica.. Infect Immun 1998 Oct;66(10):4579-87.
      7. Brackelsberg CA, Nolan LK, Brown J. Characterization of Salmonella dublin and Salmonella typhimurium (Copenhagen) isolates from cattle.. Vet Res Commun 1997 Aug;21(6):409-20.
        doi: 10.1023/A:1005803301827pubmed: 9266660google scholar: lookup
      8. Calvert N, Stewart WC, Reilly WJ. Salmonella typhimurium DT104 infection in people and animals in Scotland: a collaborative epidemiological study 1993-96.. Vet Rec 1998 Sep 26;143(13):351-4.
        doi: 10.1136/vr.143.13.351pubmed: 9800300google scholar: lookup
      9. Coburn B, Grassl GA, Finlay BB. Salmonella, the host and disease: a brief review.. Immunol Cell Biol 2007 Feb-Mar;85(2):112-8.
        doi: 10.1038/sj.icb.7100007pubmed: 17146467google scholar: lookup
      10. Cummings KJ, Warnick LD, Alexander KA, Cripps CJ, Gröhn YT, James KL, McDonough PL, Reed KE. The duration of fecal Salmonella shedding following clinical disease among dairy cattle in the northeastern USA.. Prev Vet Med 2009 Nov 1;92(1-2):134-9.
      11. Department of Agriculture, Forestry & Fisheries , 1984, Animal Diseases Act 1984 (Act 35 of 1984), Republic of South Africa.
      12. EFSA. Scientific opinion of the panel on biological hazards on a request from the European Commission on a quantitative microbiological risk assessment on Salmonella in meat: Source attribution for human salmonellosis from meat. EFSA Journal 625, 1–32.
      13. Giles N, Hopper SA, Wray C. Persistence of S. typhimurium in a large dairy herd.. Epidemiol Infect 1989 Oct;103(2):235-41.
        doi: 10.1017/S0950268800030582pmc: PMC2249503pubmed: 2680543google scholar: lookup
      14. Gordon MA. Salmonella infections in immunocompromised adults.. J Infect 2008 Jun;56(6):413-22.
        doi: 10.1016/j.jinf.2008.03.012pubmed: 18474400google scholar: lookup
      15. Grimont P.A., Weill F.-X.. Antigenic formulae of the Salmonella Serovars. 9th edn., WHO Collaborating Centre for Reference and Research on Salmonella, Institut Pasteur, Paris.
      16. Huston CL, Wittum TE, Love BC. Persistent fecal Salmonella shedding in five dairy herds.. J Am Vet Med Assoc 2002 Mar 1;220(5):650-5.
        doi: 10.2460/javma.2002.220.650pubmed: 12418526google scholar: lookup
      17. Keddy KH, Takuva S, Musekiwa A, Puren AJ, Sooka A, Karstaedt A, Klugman KP, Angulo FJ. An association between decreasing incidence of invasive non-typhoidal salmonellosis and increased use of antiretroviral therapy, Gauteng Province, South Africa, 2003-2013.. PLoS One 2017;12(3):e0173091.
      18. Kidanemariam A, Engelbrecht M, Picard J. Retrospective study on the incidence of Salmonella isolations in animals in South Africa, 1996 to 2006.. J S Afr Vet Assoc 2010 Mar;81(1):37-44.
        doi: 10.4102/jsava.v81i1.94pubmed: 20649153google scholar: lookup
      19. Kim LM, Morley PS, Traub-Dargatz JL, Salman MD, Gentry-Weeks C. Factors associated with Salmonella shedding among equine colic patients at a veterinary teaching hospital.. J Am Vet Med Assoc 2001 Mar 1;218(5):740-8.
        doi: 10.2460/javma.2001.218.740pubmed: 11280409google scholar: lookup
      20. Kimura AC, Reddy V, Marcus R, Cieslak PR, Mohle-Boetani JC, Kassenborg HD, Segler SD, Hardnett FP, Barrett T, Swerdlow DL. Chicken consumption is a newly identified risk factor for sporadic Salmonella enterica serotype Enteritidis infections in the United States: a case-control study in FoodNet sites.. Clin Infect Dis 2004 Apr 15;38 Suppl 3:S244-52.
        doi: 10.1086/381576pubmed: 15095196google scholar: lookup
      21. Mead PS, Slutsker L, Dietz V, McCaig LF, Bresee JS, Shapiro C, Griffin PM, Tauxe RV. Food-related illness and death in the United States.. Emerg Infect Dis 1999 Sep-Oct;5(5):607-25.
        doi: 10.3201/eid0505.990502pmc: PMC2627714pubmed: 10511517google scholar: lookup
      22. Morgan E, Campbell JD, Rowe SC, Bispham J, Stevens MP, Bowen AJ, Barrow PA, Maskell DJ, Wallis TS. Identification of host-specific colonization factors of Salmonella enterica serovar Typhimurium.. Mol Microbiol 2004 Nov;54(4):994-1010.
      23. Muvhali M, Smith AM, Rakgantso AM, Keddy KH. Investigation of Salmonella Enteritidis outbreaks in South Africa using multi-locus variable-number tandem-repeats analysis, 2013-2015.. BMC Infect Dis 2017 Oct 2;17(1):661.
        doi: 10.1186/s12879-017-2751-8pmc: PMC5625639pubmed: 28969587google scholar: lookup
      24. National Institute of Communicable Diseases. Salmonella Typhi cases in South Africa, 2016. Communicable Diseases Communique 2016, vol. 15(2), p. 1, Sandringham, Republic of South Africa.
      25. Padungtod P, Kadohira M, Hill G. Livestock production and foodborne diseases from food animals in Thailand.. J Vet Med Sci 2008 Sep;70(9):873-9.
        doi: 10.1292/jvms.70.873pubmed: 18840959google scholar: lookup
      26. Pascopella L, Raupach B, Ghori N, Monack D, Falkow S, Small PL. Host restriction phenotypes of Salmonella typhi and Salmonella gallinarum.. Infect Immun 1995 Nov;63(11):4329-35.
      27. Peek SE, Hartmann FA, Thomas CB, Nordlund KV. Isolation of Salmonella spp from the environment of dairies without any history of clinical salmonellosis.. J Am Vet Med Assoc 2004 Aug 15;225(4):574-7.
        doi: 10.2460/javma.2004.225.574pubmed: 15344366google scholar: lookup
      28. Popoff M.Y.. Antigenic formula of the Salmonella serovars. 8th edn., WHO Collaborating Centre for Reference and Research on Salmonella, Institut Pasteur, Paris.
      29. Rabsch W, Andrews HL, Kingsley RA, Prager R, Tschäpe H, Adams LG, Bäumler AJ. Salmonella enterica serotype Typhimurium and its host-adapted variants.. Infect Immun 2002 May;70(5):2249-55.
      30. Refsum T, Heir E, Kapperud G, Vardund T, Holstad G. Molecular epidemiology of Salmonella enterica serovar typhimurium isolates determined by pulsed-field gel electrophoresis: comparison of isolates from avian wildlife, domestic animals, and the environment in Norway.. Appl Environ Microbiol 2002 Nov;68(11):5600-6.
      31. Rice DH, Besser TE, Hancock DD. Epidemiology and virulence assessment of Salmonella dublin.. Vet Microbiol 1997 May;56(1-2):111-24.
        doi: 10.1016/S0378-1135(96)01352-1pubmed: 9228687google scholar: lookup
      32. Uzzau S, Brown DJ, Wallis T, Rubino S, Leori G, Bernard S, Casadesús J, Platt DJ, Olsen JE. Host adapted serotypes of Salmonella enterica.. Epidemiol Infect 2000 Oct;125(2):229-55.
        doi: 10.1017/S0950268899004379pmc: PMC2869595pubmed: 11117946google scholar: lookup
      33. Vanselow BA, Hum S, Hornitzky MA, Eamens GJ, Quinn K. Salmonella Typhimurium persistence in a Hunter Valley dairy herd.. Aust Vet J 2007 Nov;85(11):446-50.
      34. Veling J, Wilpshaar H, Frankena K, Bartels C, Barkema HW. Risk factors for clinical Salmonella enterica subsp. enterica serovar Typhimurium infection on Dutch dairy farms.. Prev Vet Med 2002 Jun 25;54(2):157-68.
        doi: 10.1016/S0167-5877(02)00023-5pubmed: 12069778google scholar: lookup
      35. Voetsch AC, Van Gilder TJ, Angulo FJ, Farley MM, Shallow S, Marcus R, Cieslak PR, Deneen VC, Tauxe RV. FoodNet estimate of the burden of illness caused by nontyphoidal Salmonella infections in the United States.. Clin Infect Dis 2004 Apr 15;38 Suppl 3:S127-34.
        doi: 10.1086/381578pubmed: 15095181google scholar: lookup
      36. Warnick LD, Crofton LM, Pelzer KD, Hawkins MJ. Risk factors for clinical salmonellosis in Virginia, USA cattle herds.. Prev Vet Med 2001 May 1;49(3-4):259-75.
        doi: 10.1016/S0167-5877(01)00172-6pubmed: 11311958google scholar: lookup

      Citations

      This article has been cited 9 times.
      1. Koolman L, Prakash R, Diness Y, Msefula C, Nyirenda TS, Olgemoeller F, Wigley P, Perez-Sepulveda B, Hinton JCD, Owen SV, Feasey NA, Ashton PM, Gordon MA. Case-control investigation of invasive Salmonella disease in Malawi reveals no evidence of environmental or animal transmission of invasive strains, and supports human to human transmission.. PLoS Negl Trop Dis 2022 Dec;16(12):e0010982.
        doi: 10.1371/journal.pntd.0010982pubmed: 36508466google scholar: lookup
      2. Ikhimiukor OO, Oaikhena AO, Afolayan AO, Fadeyi A, Kehinde A, Ogunleye VO, Aboderin AO, Oduyebo OO, Elikwu CJ, Odih EE, Komolafe I, Argimón S, Egwuenu A, Adebiyi I, Sadare OA, Okwor T, Kekre M, Underwood A, Ihekweazu C, Aanensen DM, Okeke IN. Genomic characterization of invasive typhoidal and non-typhoidal Salmonella in southwestern Nigeria.. PLoS Negl Trop Dis 2022 Aug;16(8):e0010716.
        doi: 10.1371/journal.pntd.0010716pubmed: 36026470google scholar: lookup
      3. Kipper D, Mascitti AK, De Carli S, Carneiro AM, Streck AF, Fonseca ASK, Ikuta N, Lunge VR. Emergence, Dissemination and Antimicrobial Resistance of the Main Poultry-Associated Salmonella Serovars in Brazil.. Vet Sci 2022 Aug 3;9(8).
        doi: 10.3390/vetsci9080405pubmed: 36006320google scholar: lookup
      4. Teng L, Liao S, Zhou X, Jia C, Feng M, Pan H, Ma Z, Yue M. Prevalence and Genomic Investigation of Multidrug-Resistant Salmonella Isolates from Companion Animals in Hangzhou, China.. Antibiotics (Basel) 2022 May 5;11(5).
        doi: 10.3390/antibiotics11050625pubmed: 35625269google scholar: lookup
      5. Alemu A, Regassa F, Kebede N, Ambachew R, Girma M, Asefa Z, Tsegaye W. Magnitude and Antimicrobial Susceptibility Profile of Salmonella Recovered from Export Abattoirs Located in East Shewa, Ethiopia.. Infect Drug Resist 2022;15:1353-1365.
        doi: 10.2147/IDR.S348773pubmed: 35386294google scholar: lookup
      6. Napoleoni M, Villa L, Barco L, Busani L, Cibin V, Lucarelli C, Tiengo A, Dionisi AM, Conti F, Da Silva Nunes FR, Tantucci L, Staffolani M, Silenzi V, Fraticelli R, Morandi B, Blasi G, Rocchegiani E, Fisichella S, On Behalf Of The Enter-Net And Enter-Vet Peripheral Laboratories Referents For Marche Region. A Strong Evidence Outbreak of Salmonella Enteritidis in Central Italy Linked to the Consumption of Contaminated Raw Sheep Milk Cheese.. Microorganisms 2021 Nov 29;9(12).
        doi: 10.3390/microorganisms9122464pubmed: 34946066google scholar: lookup
      7. Carroll LM, Pierneef R, Mathole M, Matle I. Genomic Characterization of Endemic and Ecdemic Non-typhoidal Salmonella enterica Lineages Circulating Among Animals and Animal Products in South Africa.. Front Microbiol 2021;12:748611.
        doi: 10.3389/fmicb.2021.748611pubmed: 34671335google scholar: lookup
      8. Yang C, Shao W, Wei L, Chen L, Zhu A, Pan Z. Subtyping Salmonella isolated from pet dogs with multilocus sequence typing (MLST) and clustered regularly interspaced short palindromic repeats (CRISPRs).. AMB Express 2021 Apr 24;11(1):60.
        doi: 10.1186/s13568-021-01221-9pubmed: 33893895google scholar: lookup
      9. Wei L, Yang C, Shao W, Sun T, Wang J, Zhou Z, Chen C, Zhu A, Pan Z. Prevalence and Drug Resistance of Salmonella in Dogs and Cats in Xuzhou, China.. J Vet Res 2020 Jun;64(2):263-268.
        doi: 10.2478/jvetres-2020-0032pubmed: 32587913google scholar: lookup