Development and Validation of an Indirect and Blocking ELISA for the Serological Diagnosis of African Swine Fever

被引:0
|
作者
Onyilagha, Chukwunonso [1 ]
Quizon, Kaye [2 ]
Zhmendak, Dmytro [1 ]
El Kanoa, Ian [1 ]
Truong, Thang [2 ]
Ambagala, Thanuja [1 ]
Clavijo, Alfonso [3 ]
Le, Van Phan [4 ]
Babiuk, Shawn [1 ,5 ]
Ambagala, Aruna [1 ,6 ]
机构
[1] Canadian Food Inspect Agcy, Natl Ctr Foreign Anim Dis, Winnipeg, MB R3E 3M4, Canada
[2] Publ Hlth Agcy Canada, Natl Microbiol Lab, Winnipeg, MB R3E 3M4, Canada
[3] ARS, Natl Bio & Agrodef Facil, USDA, Manhattan, KS 66506 USA
[4] Vietnam Natl Univ Agr, Coll Vet Med, Dept Microbiol & Infect Dis, Hanoi 100000, Vietnam
[5] Univ Manitoba, Dept Immunol, Winnipeg, MB R3E 0T5, Canada
[6] Univ Calgary, Fac Vet Med, Dept Comparat Biol, Calgary, AB T2N 1N4, Canada
来源
PATHOGENS | 2024年 / 13卷 / 11期
关键词
African swine fever; diagnostics; indirect ELISA; blocking ELISA; serology; HIGH-LEVEL EXPRESSION; REAL-TIME PCR; DOMESTIC PIGS; VIRUS; SERODIAGNOSIS; BACULOVIRUS; PROTEINS; ISOLATE; ASSAY; P-30;
D O I
10.3390/pathogens13110981
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
African swine fever (ASF) is an economically devastating viral disease of pigs caused by the ASF virus (ASFV). The rapid global spread of ASF has increased the demand for ASF diagnostics to be readily available and accessible. No commercial ASF enzyme-linked immunosorbent assay (ELISA) kits are manufactured and licensed in North America. Here, we report the development of two serological diagnostic assays, a blocking ELISA (bELISA) based on ASFV glycoprotein p54 and an indirect ELISA (iELISA) based on ASFV glycoproteins p54 and p72. The assays showed high sensitivity and specificity and detected anti-ASFV antibodies in serum samples from experimentally infected animals as early as 8 days post-infection. The two assays were produced commercially (AsurDx (TM) bELISA and iELISA) and subjected to extensive validation. Based on data from a set of characterized reference sera, the prototype commercial assays, while maintaining 100.00% specificity, showed 97.67% (AsurDx (TM) bELISA) and 83.72% (AsurDx (TM) iELISA) sensitivity. Both prototype assays detected anti-ASFV antibodies in serum samples collected from pigs experimentally infected with multiple ASFV strains and field samples collected from sick, recovering, and vaccinated animals. The two commercially available assays can be used in routine ASF diagnostics, serological surveys, and for evaluating serological responses to ASF vaccine candidates.
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页数:22
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