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Contact:
Dr. Gavin Thomson: gavin@tadscientific.co.za
tel/fax: +27 12 348 6891
cell: +27 82 33 66 088
Dr. Marylou Penrith: marylou@teledata.mz
tel: +25 8 213225431
cell: +258 827 180 560
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Thomson, G R, Tambi, E N, Hargreaves, S K, Leyland
T J, Catley A P, van’t
Klooster, G G M & Penrith, M-L, (2004). International trade in livestock
and livestock products: The need for a commodity-based approach. The Veterinary
Record (2004) 155,429-433
Summary
International animal health standards designed to facilitate safe trade
in livestock and livestock products are set by the Office International
des Epizooties (OIE)
under the Sanitary and Phytosanitary Agreement of the World Trade Organization
(WTO) and documented in the OIE’s Terrestrial Animal Health Code (the Code).
A core principle of the Code is the need for countries to eradicate important
transboundary animal diseases (TADs) to reduce the risk of exporting disease
to trading partners. International food safety standards are set by the Codex
Alimentarius Commission, administered jointly by the World Health Organization
and the Food and Agriculture Organization.The goal of global eradication of most
TADs is unachievable for the foreseeable future, other than in the case of rinderpest,
and this prevents many countries from engaging in international trade under WTO
rules, especially developing nations. An alternative commodity-based approach
is proposed to the formulation of international animal health and food safety
standards based on the fact that different commodities pose very different risks
when it comes to spread of human and animal pathogens. Therefore, the risk mitigation
strategies required are equally commodity dependent. We conclude that more focused
commodity standards would improve access to international markets for all countries,
especially those in the developing world. For this objective to be realized,
credible and independent certification is required.
To view full article as a PDF, click here
Penrith , M-L, Thomson G R, Bastos, A D S, Phiri O C, Lubisi B A, Du Plessis
E C, Macome, F, Pinto F, Botha B & Esterhuysen J, (in press). An investigation
into natural resistance to African swine fever in domestic pigs from an endemic
area in southern Africa. OIE Scientific and technical Review.
Summary
A population of domestic pigs in northern Moçambique with increased resistance
to the pathogenic effects of African swine fever (ASF) virus was identified by
the high prevalence of circulating antibodies to ASF virus. An attempt was made
to establish whether the resistance in this population was heritable. Some of
these pigs were acquired and transported to a quarantine facility and allowed
to breed naturally. Offspring of the resistant pigs were transferred to a high
security facility where they were challenged with two ASF viruses, one of which
was isolated from the population of pigs from which the Mocambiquan pigs were
derived and the other a genetically closely-related virus from Madagascar. All
but one of the 105 offspring challenged developed acute ASF and died. It therefore
appears that the resistance demonstrated by these pigs is not inherited by their
offspring, or could not be expressed under the conditions of the experiment.
The question remains therefore as to the mechanism whereby pigs in the population
from which the experimental pigs were derived co-existed with virulent ASF viruses.
Bastos, A D S, Penrith M-L, Crucière C, Edrich J L, Hutchings G, Roger,
F, Couacy-Hymann, E & Thomson G R, 2003. Genotyping field strains of African
swine fever virus by partial p72 gene characterization. Archives of Virology,
148, 693-706.
Summary
A PCR sequencing method was developed which permits detection and characterization
of African swine fever virus (ASFV) variants within 5 and 48h, respectively,
of receipt of a clinical specimen. Amplification of a 478 bp fragment corresponding
to the C-terminal end of the p72 gene confirms virus presence with gene characterization
being achieved by nucleotide sequence determination and phylogenetic analysis.
The method was applied to 55 viruses including those representative of the major
ASF lineages identified previously by restriction fragment length polymorphism
(RFLP) analysis. Results confirmed that the p72 method identifies the same major
viral groupings. Characterization of additional viruses of diverse geographical,
species and temporal origin using the PCR-based method indicated the presence
of 10 major ASF genotypes on the African continent, the largest of which comprised
a group of genetically homogeneous viruses recovered from outbreaks in Europe,
South America, the Caribbean and West Africa (the ESAC-WA genotype). In contrast
viruses from southern and eastern African countries were heterogeneous with multiple
genotypes being present within individual countries. This study provides a rapid
and accurate method of determining the genotype of field and outbreak strains
of ASF and is therefore useful for molecular epidemiological clarification of
ASF.
Thomson G R, Vosloo W & Bastos A D S, (2003). Foot and mouth disease in wildlife.
Virus Research, 91, 145-161.
No published summary. Thomson G, Dungu B, Tounkara K, Vosloo W, Bastos A. & Bidjeh
K, 2003. Suitability of currently available vaccines for controlling the major
transboundary diseases that afflict sub-Saharan Africa. In: Vaccines for List
A and Emerging Animal Diseases. Brown, F. & Roth, J. (eds), 114, 229-241.
Karger: Basel.
No published summary.
Bastos A D S., Haydon D T, Sangare O, Boshoff C I, Edrich J L & Thomson G
R (2003). The implications of viral diversity within the SAT-2 serotype for control
of foot-and-mouth disease in sub-Saharan Africa. Journal of General Virology,
84, 1595-1606.
Summary
SAT 2 is the serotype most often associated with outbreaks of foot-and-mouth
disease (FMD) in livestock in southern and western Africa and is the only SAT
type to have been recorded outside the African continent in the last decade.
Its epidemiology is complicated by the presence of African buffalo (Syncerus
caffer), which play an important role in virus maintenance and transmission.
To assess the level of genetic complexity of this serotype among viruses associated
with both domestic livestock and wildlife, complete VP1 gene sequences for 53
viruses from 17 countries and three different host species were analysed. Phylogenetic
analysis revealed eleven virus lineages, differing from each other by at least
20% in pairwise nucleotide comparisons, four of which fall within the southern
African region, two in West Africa and the remaining 5 in central and East Africa.
No evidence of recombination between these lineages was detected, and thus we
conclude that these are independently evolving virus lineages which occur primarily
in discrete geographical localities in accordance with the FMD virus topotype
concept. Applied to the whole phylogeny, rates of nucleotide substitution are
significantly different between topotypes, but most individual topotypes evolve
in accordance with a molecular clock at an average rate of approximately 0.002
substitutions per site per year. This study provides an indication of the intratypic
complexity of the SAT 2 serotype at the continental level and emphasizes the
value of molecular characterization of diverse FMD field strains for tracing
the origin of outbreaks.
Thomson G R, Bengis R G & Brown C (2001). Picornaviruses. In: Infectious
Diseases of Wild Mammals, 3rd Edn., E.S. Williams & I.K. Barker (eds.), pp
119-130, Iowa University Press: Ames, USA.
No summary published.
Scott Wilson Resource Consultants, 2000. Environmental impact assessment
of the veterinary fences in Ngamiland. Six volume report plus a summary
report for the
Government of Botswana. Study jointly funded by the Department for International
Development (UK) and the Government of Botswana.Full publication lists available
on request
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