Your browser doesn't support javascript.
loading
Seroprevalence of Rift Valley fever virus in cattle in the Democratic Republic of the Congo.
Tshilenge, Georges Mbuyi; Dundon, William G; De Nardi, Marco; Mulumba Mfumu, Leopold K; Rweyemamu, Mark; Kayembe-Ntumba, Jean-Marie; Masumu, Justin.
Affiliation
  • Tshilenge GM; Faculty of Veterinary Medicine, University of Kinshasa, University Street, P.O. Box 117, Kinshasa XI, Democratic Republic of the Congo. tshilenge.georges@gmail.com.
  • Dundon WG; Central Veterinary Laboratory, Wangata Street, Gombe, P.O. Box 8842, Kinshasa, Democratic Republic of the Congo. tshilenge.georges@gmail.com.
  • De Nardi M; Animal Production and Health Laboratory, Joint FAO/AIEA, Division of Nuclear Techniques in Food and Agriculture, Department of Nuclear Sciences and Application, International Atomic Energy Agency, Wagramer Strasse 5, P.O. Box 100, 1400, Vienna, Austria.
  • Mulumba Mfumu LK; SAFOSO, Waldeggstrasse 1, 3097, Liebefeld, Switzerland.
  • Rweyemamu M; Faculty of Veterinary Medicine, University of Kinshasa, University Street, P.O. Box 117, Kinshasa XI, Democratic Republic of the Congo.
  • Kayembe-Ntumba JM; Southern African Centre for Infectious Disease Surveillance, Sokoïne University of Agriculture, Chuo Kikuu, P.O. Box 3297, Morogoro, Tanzania.
  • Masumu J; Faculty of Medicine, University of Kinshasa, University Street, P.O. Box 117, Kinshasa XI, Democratic Republic of the Congo.
Trop Anim Health Prod ; 51(3): 537-543, 2019 Mar.
Article in En | MEDLINE | ID: mdl-30350160
ABSTRACT
This study aimed at assessing the serological and virological status of Rift Valley fever virus (RVFV) in cattle from four climatically diverse zones of the Democratic Republic of the Congo (DRC). A total of 1675 sera samples collected between 2014 and 2015 from cattle without clinical manifestation of RVF infection were tested using competitive and capture enzyme ELISA to detect both IgG and IgM. RT-PCR was used for the detection of nucleic acid of RVFV. Out of the 1675 cattle sera tested, 203 were found to be IgG-positive, giving an overall true seroprevalence of 12.37% (95% CI 10.86-14.05). This seroprevalence varied between the four zones with a seroprevalence of 16.16% (95% CI 12.86-20.12), 14.70% (95% CI 11.72-18.29), 10.82% (95% CI 7.19-14.19), and 7.34% (95% CI 5.13-10.41) recorded in cattle sampled in the mountainous, humid savannah, dry savannah, and forest zones, respectively (p < 0.05, χ2 = 17.26). A higher true seroprevalence of 14.58% (95% CI 9.3-22.13) was found in animals aged 1 year compared to 10.43% (95% CI 8.12-13.30) and 13.16% (95% CI 11.19-15.42) in groups aged between 2-3 and > 3 years, respectively, although the difference was not statistically significant (p > 0.05, χ2 = 2.95). Similarly, no statistically significant difference (p > 0.05, χ2 = 0.04) was found between the sexes of the animals. Among the IgG-positive samples screened for anti-RVFV IgM, only 1.47% (3/203) was IgM-positive. One of the IgM-positive samples was positive by RT-PCR. These findings reveal country-wide distribution of RVF in the DRC for the first time.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rift Valley Fever / Rift Valley fever virus / Cattle Diseases Limits: Animals Country/Region as subject: Africa Language: En Journal: Trop Anim Health Prod Year: 2019 Document type: Article Affiliation country: Democratic Republic of the Congo

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rift Valley Fever / Rift Valley fever virus / Cattle Diseases Limits: Animals Country/Region as subject: Africa Language: En Journal: Trop Anim Health Prod Year: 2019 Document type: Article Affiliation country: Democratic Republic of the Congo