2007
DOI: 10.3201/eid1309.070466
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Mokola Virus in Domestic Mammals, South Africa

Abstract: We recently identified 2 Mokola viruses from domestic mammals (a dog and a cat) in South Africa. These cases occurred 8 years after the last reported case of infection with this virus. Our findings emphasize the endemicity of rabies-related lyssaviruses in South Africa and the need to better understand the epidemiology of Mokola viruses.

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Cited by 40 publications
(37 citation statements)
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“…Samples were selected based on previous phylogenetic studies to be representative of different phylogenetic groups within each genotype (Nel et al 2005;Sabeta et al 2007;Cohen, Sartorius, Sabeta, Zulu, Paweska, Mogoswane, Sutton, Nel, Swanepoel, Leman, Grobbelaar, Dayson & Blumberg 2007;Markotter, Kuzmin, Rupprecht & Nel 2008).…”
Section: Samplesmentioning
confidence: 99%
“…Samples were selected based on previous phylogenetic studies to be representative of different phylogenetic groups within each genotype (Nel et al 2005;Sabeta et al 2007;Cohen, Sartorius, Sabeta, Zulu, Paweska, Mogoswane, Sutton, Nel, Swanepoel, Leman, Grobbelaar, Dayson & Blumberg 2007;Markotter, Kuzmin, Rupprecht & Nel 2008).…”
Section: Samplesmentioning
confidence: 99%
“…Although indications are that some LBV isolates or variants are highly pathogenic in mouse models compared to invasive RABV strains, no confirmed human cases have been linked to infection with the virus as of yet . Among the lyssaviruses the epidemiology of MOKV is particularly obscure and the virus has been infrequently isolated from several animal species, including domestic dogs, cats and shrews in the past 30 years (Sabeta et al, 2007b). On various occasions, cases of fatal MOKV infections in dogs and cats occurred in animals with rabies vaccination histories (Nel et al, 2000) however MOKV has not been associated with definitive human rabies cases .…”
Section: Introductionmentioning
confidence: 99%
“…The RNA pellet was solubilised in 50 μl of RNase-free water, quantified spectrophotometrically and stored at −70°C until required for RT-PCR. Approximately 1 μg of the total viral RNA was included in a reaction mixture that consisted of Lys001 (+) (20 pmoles), 200 units of Murine Moloney Leukemia Virus Reverse Transcriptase (M-MLV, USB ™ ), 20 units of RNasin® ribonuclease inhibitor (Promega), 20 mM of dNTP mixture, 0.2M DTT and 5X M-MLV reaction buffers as described previously (Sabeta et al, 2007). The cDNA synthesis mixture was inactivated at 70°C for 10 minutes, diluted two-fold with sterile nuclease free water and stored at −20°C until further use.…”
Section: Methodsmentioning
confidence: 99%