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Study on the efficacy of Leptospira vaccines developed from serovars isolated from Trinidad and comparison with commercial vaccines using a hamster model
Suepaul, S. M. ; Carrington, C. V. ; Campbell, M. ; Borde, G. ; Adesiyun, A. A. .
Affiliation
  • Suepaul, S. M. ; The University of The West Indies. Faculty of Medical Sciences. School of Veterinary Medicine. St. Augustine. Trinidad and Tobago
  • Carrington, C. V. ; The University of The West Indies. Faculty of Medical Sciences. School of Medicine. St. Augustine. Trinidad and Tobago
  • Campbell, M. ; The University of The West Indies. Faculty of Medical Sciences. School of Veterinary Medicine. St. Augustine. Trinidad and Tobago
  • Borde, G. ; The University of The West Indies. Faculty of Medical Sciences. School of Veterinary Medicine. St. Augustine. Trinidad and Tobago
  • Adesiyun, A. A. ; The University of The West Indies. Faculty of Medical Sciences. School of Veterinary Medicine. St. Augustine. Trinidad and Tobago
Vaccine ; 28(33): 5421-5426, Jun. 19 2010. tab, graf
Article in English | MedCarib | ID: med-17679
Responsible library: TT5
ABSTRACT
A hamster model was used to determine the efficacy of commercially prepared canine vaccines against Leptospira serovars circulating in Trinidad and to assess the effectiveness of killed whole-cell vaccines prepared from local isolates. The local isolates used for vaccine preparation and challenge were isolates of serovars Copenhageni and Mankarso obtained from a local dog and rodent. Their estimated lethal dose-50 (LD(50)) were 5 and 10 organisms, respectively and clinical signs observed on infection were consistent with leptospirosis. An unvaccinated control group of hamsters and other groups of hamsters that had been vaccinated with 3 doses of (i) in-house whole-cell Copenhageni vaccine, (ii) in-house whole-cell Mankarso vaccine, (iii) commercial vaccine Brand A or (iv) commercial vaccines Brand B were challenged with 1000 times the LD(50) of the respective challenge serovar. The most commonly used commercial vaccine (Brand A) did not offer protection to challenged hamsters, whereas Brand B facilitated the renal carrier state of the Leptospira organism. In contrast the whole-cell vaccines developed from local strains of serovars Copenhageni and Mankarso, protected all hamsters tested from both clinical disease and renal carrier states.
Subject(s)
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Collection: International databases Health context: Sustainable Health Agenda for the Americas / SDG3 - Health and Well-Being Health problem: Goal 10: Communicable diseases / Target 3.3: End transmission of communicable diseases Database: MedCarib Main subject: Trinidad and Tobago / Vaccines / Leptospira / Leptospirosis Limits: Animals / Humans Country/Region as subject: English Caribbean / Trinidad and Tobago Language: English Journal: Vaccine Year: 2010 Document type: Article Institution/Affiliation country: The University of The West Indies/Trinidad and Tobago
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Collection: International databases Health context: Sustainable Health Agenda for the Americas / SDG3 - Health and Well-Being Health problem: Goal 10: Communicable diseases / Target 3.3: End transmission of communicable diseases Database: MedCarib Main subject: Trinidad and Tobago / Vaccines / Leptospira / Leptospirosis Limits: Animals / Humans Country/Region as subject: English Caribbean / Trinidad and Tobago Language: English Journal: Vaccine Year: 2010 Document type: Article Institution/Affiliation country: The University of The West Indies/Trinidad and Tobago
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