Application of the Ceditest® FMDV type O and FMDV-NS enzyme-linked immunosorbent assays for detection of antibodies against Foot-and-mouth disease virus in selected livestock and wildlife species in Uganda

被引:4
作者
Ayebazibwe, Chrisostom [2 ]
Mwiine, Frank Norbert [2 ]
Balinda, Sheila Nina [3 ]
Tjornehoj, Kirsten [1 ]
Alexandersen, Soren [1 ]
机构
[1] Tech Univ Denmark, Natl Vet Inst, DK-4771 Lindholm, Kalvehave, Denmark
[2] Minist Agr Anim Ind & Fisheries, Entebbe, Uganda
[3] Makerere Univ, Inst Environm & Nat Resources, Kampala, Uganda
关键词
Ceditest (R) FMDV-NS; Ceditest (R) FMDV type O; Foot-and-mouth disease; Uganda; BUFFALOS SYNCERUS-CAFFER; NONSTRUCTURAL PROTEINS; EXPERIMENTAL INFECTION; SMALL RUMINANTS; CATTLE; VACCINATION; DIFFERENTIATION; ANTIGENS; AFRICA; ELISA;
D O I
10.1177/1040638711435807
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Diagnosis and control of Foot-and-mouth disease virus (FMDV) requires rapid and sensitive diagnostic tests. Two antibody enzyme-linked immunosorbent assay (ELISA) kits, Ceditest (R) FMDV-NS for the detection of antibodies against the nonstructural proteins of all FMDV serotypes and Ceditest (R) FMDV type O for the detection of antibodies against serotype O, were evaluated under African endemic conditions where the presence of multiple serotypes and the use of nonpurified vaccines complicate serological diagnosis. Serum samples from 218 African buffalo, 758 cattle, 304 goats, and 88 sheep were tested using both kits, and selected samples were tested not only in serotype-specific ELISAs for antibodies against primarily FMDV serotype O, but also against other serotypes. The FMDV-NS assay detected far more positive samples (93%) than the FMDV type O assay (30%) in buffalo (P < 0.05), with predominant antibodies against the South African Territories (SAT) serotypes, while the seroprevalence was generally comparable in cattle with antibodies against serotype O elicited by infection and/or vaccination. However, some districts had higher seroprevalence using the FMDV type O assay indicating vaccination without infection, while 1 cattle herd with antibodies against the SAT serotypes had far more positive samples (85%) using the FMDV-NS versus the FMDV type O (10%), consistent with the latter test's lower sensitivity for antibodies against SAT serotypes. Based on the current investigation, the FMDV type O ELISA may be limited by the presence of SAT serotypes. The FMD NS assay worked well as a screening test for antibodies against all FMDV serotypes present in Uganda; however, as long as nonpurified vaccines are applied in the region, this test cannot be used to differentiate between vaccinated and infected animals.
引用
收藏
页码:270 / 276
页数:7
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