Evaluation of a new sandwich ELISA kit that uses serum for detection of cattle persistently infected with BVD virus

被引:0
作者
Saliki, JT [1 ]
Huchzermeier, R
Dubovi, EJ
机构
[1] Oklahoma State Univ, Oklahoma Anim Dis Diagnost Lab, Stillwater, OK 74078 USA
[2] Syracuse Bioanalyt, Ithaca, NY 14850 USA
[3] Cornell Univ, NYSCVM, Diagnost Lab, Ithaca, NY 14853 USA
来源
TROPICAL VETERINARY DISEASES: CONTROL AND PREVENTION IN THE CONTEXT OF THE NEW WORLD ORDER | 2000年 / 916卷
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中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cattle immunotolerant to and persistently infected (PI) with bovine viral diarrhea (BVD) virus (BVDV) constitute the mechanism by which BVDV persists in and spreads among cattle herds. Detection and elimination of PI cattle are necessary for control of BVD. Serum is an excellent specimen for BVD PI testing because of high survivability of BVDV in serum and ease of collection, storage, and handling. Currently, microtiter virus isolation (VI) employing serum and sandwich ELISAs (S-ELISA) on tissues or leukocytes are used for BVDV PI screening. This paper evaluates a new S-ELISA kit that uses serum as the diagnostic sample. Cattle sera (n = 408) were tested using VI and the S-ELISA. The VI detected 172 BVDV-positive sera. Of these, 18 were confirmed PI cattle. The S-ELISA was positive on all PI samples. Considering only the PI animals, and using VI as the gold standard, the relative sensitivity of S-ELISA was 100%. The overall relative sensitivity was 93.6% and the agreement quotient (kappa) was 0.94. The relative specificity of the kit, based on 236 VI-negative sera, was 100%. These data indicate that the new kit is very adequate for detection of BVDV PI cattle.
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页码:358 / 363
页数:6
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