https://jvmoh.org/index.php/jvmoh/issue/feed Journal of Veterinary Medicine and One Health 2021-03-15T10:48:00-07:00 Open Journal Systems <div class="block paragraph" data-block="true" data-editor="8bkv0" data-offset-key="fvov1-0-0"> <div class="public-DraftStyleDefault-block public-DraftStyleDefault-ltr" data-offset-key="fvov1-0-0"><span data-offset-key="fvov1-0-0">The </span><em>Journal of Veterinary Medicine and One Health,&nbsp;</em><span data-offset-key="fvov1-0-2">an open access journal of the Kenya Veterinary Association (previously published as the&nbsp;<em>Kenya Veterinarian).</em></span></div> </div> <div class="block paragraph" data-block="true" data-editor="8bkv0" data-offset-key="9lftt-0-0"> <div class="public-DraftStyleDefault-block public-DraftStyleDefault-ltr" data-offset-key="9lftt-0-0">&nbsp;</div> </div> https://jvmoh.org/index.php/jvmoh/article/view/13 Animal Health, Human Health and Development 2021-03-15T10:48:00-07:00 S M Thumbi thumbi.mwangi@wsu.edu C N Kimwele ckimwele@uonbi.ac.ke <p>No Abstract.</p> 2019-12-14T00:00:00-08:00 ##submission.copyrightStatement## https://jvmoh.org/index.php/jvmoh/article/view/11 The World Organization for Animal Health (OIE)’s engagement towards Rabies Elimination in Africa 2021-03-15T10:47:59-07:00 Samuel Wanyangu Wakhusama srr.eastern-africa@oie.int Patrick Bastiaensen srr.eastern-africa@oie.int Rachid Bouguedour rsr.afriquedunord@oie.int Moetapele Letshwenyo srr.southern-africa@oie.int Karim Tounkara rr.africa@oie.int Jocelyn Mérot rsr.afriquedunord@oie.int Alessandro Ripani rsr.afriquedunord@oie.int Torres Gregorio communication@oie.int Stéphane Renaudin communication@oie.int Catherine Bertrand-Ferrandis communication@oie.int Elisabeth Erlacher-Vindel communication@oie.int <p>This review article highlights the role of the World Organisation for Animal Health (OIE) towards dog-mediated rabies elimination in Africa. It provides a brief description of rabies and its global impact on humans and the role of the OIE in the elimination of dog-mediated human rabies by 2030. In addition, it addresses the OIE international standards on rabies, the Performance of Veterinary Services (PVS) Pathway as a tool to assess the quality of Veterinary Services, the partnership with other international organizations under the “One Health” umbrella as applied in the elimination of dog-mediated human rabies, the rabies vaccine bank, the training of OIE national Focal Points, and laboratory twinning projects as a means to enhance capacity in the fight against dog-mediated human rabies in Africa. The article concludes by presenting specific pilot projects being undertaken by the OIE in Africa - as proof of concept - in view of scaling up activities in the African continent.</p> 2019-12-14T14:21:38-08:00 ##submission.copyrightStatement## https://jvmoh.org/index.php/jvmoh/article/view/4 Formalin Inactivated infectious Bursal Disease Virus Vaccine Immunogenicity in Indigenous Chickens in Kenya 2021-03-15T10:47:58-07:00 Wanzila Usyu Mutinda, Dr. w.mutinda@pu.ac.ke Bebora Lily Caroline, Prof lilybebora@gmail.com Philip Njeru Nyaga, Prof pnyagaon@yahoo.co.uk Paul Gichohi Mbuthia, Prof mbuthiagichohi1@gmail.com Lucy Wanjiru Njagi, Dr. njagiluc@uonbi.ac.ke <p><strong>Background:</strong> Infectious bursal disease vaccination failure and subsequent outbreaks in vaccinated chickens are a challenge in poultry production. This could be due to use of live vaccines which may revert to virulence resulting in disease. Further, live vaccines may become non-viable due to poor handling and yield no immune response. Killed vaccines developed using indigenous strains could offer solutions to the challenge. Immunogenicity of five formalin inactivated virus isolates from field outbreaks in Kenya were determined. The isolates, designated as E3, E9, E19, E34 and, E42, were prepared at 10<sup>4</sup>EID<sub>50 </sub>and&nbsp; each inoculated into six 4 week old specific antigen negative (SAN) indigenous chicks. 0.3mls was administered intramuscularly at day 0, 14 and 21 and titres levels measured at inoculation (baseline), days 14, 21, 28 and 35.</p> <p><strong>Results:</strong>&nbsp; Immune responses were detected by Agar Gel Precipitation Test (AGPT) and Enzyme Linked Immunosorbent Assay (ELISA). All the isolates elicited detectable immune response by day 14. Antibody titre values by day 21 were above 396 and considered positive. Highest titre value (9140) was recorded on day 28 in response to E19. Titres variations between isolates were not statistically significant (<em>p</em>=0.9639).</p> <p><strong>Conclusions:</strong> All isolates were immunogenic. Isolates E3 and E19 consistently yielded high titres and were recommended as most suitable for development for use in a vaccination regimen.</p> 2019-12-14T14:23:00-08:00 ##submission.copyrightStatement##