A Five-Year Retrospective Study of Foot-and-Mouth Disease Outbreaks in Southern Africa, 2014 to 2018

Author:

Fana Elliot Mpolokang12ORCID,Mpoloka Sununguko Wata2,Leteane Melvin2,Seoke LaToya1,Masoba Kelebogile3,Mokopasetso Mokganedi4,Rapharing Aobakwe1,Kabelo Tshephang1,Made Patricia3,Hyera Joseph1

Affiliation:

1. OIE Sub-Saharan Africa Regional Reference Laboratory for Foot-and-Mouth Disease (OIE-SSARRLFMD), Botswana Vaccine Institute, Private Bag 0031, Gaborone, Botswana

2. Department of Biological Sciences, Faculty of Science, University of Botswana, Private Bag 00704, Gaborone, Botswana

3. National Veterinary Laboratory, OIE-SSARRLFMD, Botswana Vaccine, Private Bag 0031, Gaborone, Botswana

4. Veterinary Department, Botswana Vaccine Institute, Private Bag 0031, Gaborone, Botswana

Abstract

Foot-and-mouth disease (FMD) virus (FMDv), like other ribonucleic acid (RNA) genome viruses, has a tendency to mutate rapidly. As such, available vaccines may not confer enough cross-protection against incursion of new lineages and sublineages. This paper is a retrospective study to determine the topotypes/lineages that caused previous FMD outbreaks in 6 southern African countries and the efficacy of the current vaccines to protect cattle against them. A total of 453 bovine epithelial tissue samples from 33 FMD outbreaks that occurred in these countries from 2014 to 2018 were investigated for the presence of FMDv. The genetic diversity of the identified Southern African Type (SAT)-FMD viruses was determined by comparing sequences from outbreaks and historical prototype sequences. Of the 453 samples investigated, 176 were positive for four FMDv serotypes. Out of the 176 FMD positive cases there were 105 SAT2 samples, 32 SAT1 samples, 21 SAT3 samples, and 18 serotype O samples. Phylogenetic analysis grouped the SATs VP1 gene sequences into previously observed topotypes in southern Africa. SAT1 viruses were from topotypes I and III, SAT2 viruses belonged to topotypes I, II, III, and IV, and SAT3 viruses were of topotypes I and II. Vaccine matching studies on the field FMDv isolates produced r1-values greater than or equal to 0.3 for the three SAT serotypes. This suggests that there is no significant antigenic difference between current SAT FMD vaccine strains and the circulating SAT serotypes. Therefore, the vaccines are still fit-purpose for the control FMD in the region. The study did not identify incursion of any new lineages/topotypes of FMD into the sampled southern African countries.

Funder

Botswana Vaccine Institute

Publisher

Hindawi Limited

Subject

General Veterinary

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