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Dergiler / Turkish Journal of Veterinary and Animal Sciences / 2013 / Cilt: 37 - Sayı: 6

Prevalence of Shiga toxin-producing Escherichia coli and pathogenic Leptospira spp. in rodents from outdoor farms in western Spain

Sayfa
750–753
Yayın Tarihi
2013-06-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

According to these results, rats from outdoor farms may be considered a reservoir host for Leptospira in the study area.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Sixty-five rats (Rattus norvegicus) and 5 mice (Mus musculus) were trapped from 8 outdoor farms and the presence of Shiga toxin-producing Escherichia coli was not detected in any individual.
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Temel Bulgular & Veri:Nevertheless, using the microscopic agglutination test, it was found that 20% (13/65) of rat serum samples were positive for anti-Leptospira antibodies, and DNA of pathogenic leptospires was detected in 3.07% (2/65) of the rat kidneys by real-time polymerase chain reaction.
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Sonuç & Katkı:According to these results, rats from outdoor farms may be considered a reservoir host for Leptospira in the study area.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Rodents · Shiga-toxin producing Escherichia coli · Leptospira spp.

Özet

Sixty-five rats (Rattus norvegicus) and 5 mice (Mus musculus) were trapped from 8 outdoor farms and the presence of Shiga toxin-producing Escherichia coli was not detected in any individual. Nevertheless, using the microscopic agglutination test, it was found that 20% (13/65) of rat serum samples were positive for anti-Leptospira antibodies, and DNA of pathogenic leptospires was detected in 3.07% (2/65) of the rat kidneys by real-time polymerase chain reaction. The most common infecting serovar was Castellonis (7.69%), followed by Canicola (6.15%) and Mangus (6.15%). According to these results, rats from outdoor farms may be considered a reservoir host for Leptospira in the study area.

Abstract

Sixty-five rats (Rattus norvegicus) and 5 mice (Mus musculus) were trapped from 8 outdoor farms and the presence of Shiga toxin-producing Escherichia coli was not detected in any individual. Nevertheless, using the microscopic agglutination test, it was found that 20% (13/65) of rat serum samples were positive for anti-Leptospira antibodies, and DNA of pathogenic leptospires was detected in 3.07% (2/65) of the rat kidneys by real-time polymerase chain reaction. The most common infecting serovar was Castellonis (7.69%), followed by Canicola (6.15%) and Mangus (6.15%). According to these results, rats from outdoor farms may be considered a reservoir host for Leptospira in the study area.

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Bu Makaleye Atıf Yap

Anonim (2013). Prevalence of Shiga toxin-producing Escherichia coli and pathogenic Leptospira spp. in rodents from outdoor farms in western Spain. Turkish Journal of Veterinary and Animal Sciences, Cilt: 37 - Sayı: 6, 750–753. https://ajindex.com/articles/125723

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Kaynakça (11)

  1. Wangrongsarb P, Petkanchanapong W, Yasaeng S, Imvithaya A, Naigowit P. Survey of leptospirosis among rodents in epidemic areas of Thailand. J Trop Med Parasitol 2002; 25: 55–58.
  2. Cizek A, Alexa P, Literak I, Hamrik J, Novak P, Smola J. Shiga toxin-producing Escherichia coli O157 in feedlot cattle and Norwegian rats from a large-scale farm. Lett Appl Microbiol 1999; 28: 435–439. García-Sánchez A, Sánchez S, Rubio R, Pereira G, Alonso JM, Hermoso de Mendoza J, Rey J. Presence of Shiga toxinproducing E. coli O157:H7 in a survey of wild artiodactyls. Vet Microbiol 2007; 121: 373–377.
  3. Rahn K, Renwick SA, Johnson RP, Wilson JB, Clarke RC, Alves D, McEven S, Lior H, Spika J. Persistence of Escherichia coli O157:H7 in dairy cattle and dairy farm environment. Epidemiol Infect 1997; 119: 251–259.
  4. Hancock DD, Besser TE, Rice DH, Ebel ED, Herriott DE, Carpenter LV. Multiple sources of Escherichia coli O157 in feedlots and dairy farms in the northwestern USA. Prev Vet Med 1998; 35: 11–19.
  5. Nielsen EM, Skov MN, Madsen JJ, Lodal J, Jespersen JB, Baggesen DL. Verocytotoxin-producing Escherichia coli in wild birds and rodents in close proximity to farms. Appl Environ Microbiol 2004; 70: 6944–6947.
  6. Foronda P, Martin-Alonso A, Castillo-Figueruelo B, Feliu C, Gil H, Valladares B. Pathogenic Leptospira spp. in wild rodents, Canary Islands, Spain. Emerg Infect Dis 2010; 17: 1781–1782.
  7. Bharti AR, Nally JE, Ricaldi JN, Matthias MA, Diaz MM, Lovett MA, Levett PN, Gilman RH, Willig MR, Gotuzzo E et al. Leptospirosis: a zoonotic disease of global importance. Lancet Infect Dis 2003; 3: 757–771.
  8. Da Silva EF, Félix SR, Cerqueira GM, Fagundes MQ, Neto ACPS, Grassmann AA, Amaral MG, Gallina T, Dellagostin OA. Preliminary characterization of Mus musculus-derived pathogenic strains of Leptospira borgpetersenii serogroup Ballum in a hamster model. Am J Trop Med Hyg 2010; 83: 336–337.
  9. Perea A, Garcia R, Maldonado A, Tarradas MC, Luque I, Astorga R, Arenas A. Prevalence of antibodies to different Leptospira interrogans serovars in pigs on large farms. Zentralbl Veterinarmed B 1994; 41: 512–516.
  10. Rojas P, Monahan AM, Schuller S, Miller IS, Markey BK, Nally JE. Detection and quantification of leptospires in urine of dogs: a maintenance host for the zoonotic disease leptospirosis. Eur J Clin Microbiol 2010; 29: 1305–1309.
  11. Shenberg E, Birnbaum S, Radrig E, Torten M. Dynamic changes in the epidemiology of canicola fever in Israel. Natural adaptation of an established serotype to a new reservoir host.