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1.
Prev Vet Med ; 140: 30-37, 2017 May 01.
Article in English | MEDLINE | ID: mdl-28460747

ABSTRACT

Equine infectious anemia virus (EIAV) is an important cause of morbidity and mortality throughout the world. Although the virus infects all members of the Equidae the vast majority of studies have been conducted in horses (Equus caballus) with comparatively little information available for other equid species. Brazil has one of the most abundant donkey (E. asinus) populations of any nation although the economic importance of these animals is declining as transportation becomes increasingly mechanized. As a result, considerable numbers of donkeys especially in the Northeast of the country have been released and allowed pursue an almost feral existence. Consequently, this large and growing population constitutes a significant risk as a reservoir for the maintenance and transmission of important equine infectious diseases such as glanders and equine arteritis virus in addition to EIAV. This study examines the prevalence of EIA in a semi-wild donkey population from Mossoró city, in Northeast Brazil, using AGID followed by cELISA, rgp90 ELISA and immunoblot (IB). Serum samples were collected from 367 donkeys without obvious EIA clinical signs. Subsequent testing revealed seropositive rates of 1.6% (6/367) in officially approved AGID tests, 3.3% (12/367) in cELISA and 14.4% (53/367) in the rgp90 ELISA. However, 88.7% (47/53) of the rgp90 ELISA positive samples were almost certainly false reactions because they failed to react with two or more antigens in IB. Consequently, the rpg90 ELISA has a similar sensitivity to AGID with donkey serum samples. Such high false positive rates have not been observed previously with serum samples from horses. Another highly significant finding is that 56.9% (33/58) of the donkey serum samples tested in IB had reactivity to EIAV p26 only. Although this could result from recent infection with the virus, it has been found that in some equids p26 only reactivity persists for extensive periods of time suggesting exposure to antigens possessing cross-reactive determinants or EIAV strains with envelope glycoproteins that are different from any that have been previously characterized and so undetectable by current IB techniques.


Subject(s)
Equine Infectious Anemia/diagnosis , Equine Infectious Anemia/epidemiology , Immunologic Tests/veterinary , Animals , Animals, Wild , Antibodies, Viral/blood , Antigens, Viral/blood , Brazil/epidemiology , Enzyme-Linked Immunosorbent Assay/veterinary , Equidae/blood , Equine Infectious Anemia/blood , Factor Analysis, Statistical , Horses , Immunologic Tests/methods , Infectious Anemia Virus, Equine/genetics , Infectious Anemia Virus, Equine/isolation & purification , Prevalence , Sensitivity and Specificity
2.
J Virol Methods ; 180(1-2): 62-7, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22227617

ABSTRACT

Equine infectious anemia (EIA) is an important viral infection affecting horses worldwide. The course of infection is accompanied generally by three characteristic stages: acute, chronic and inapparent. There is no effective EIA vaccine or treatment, and the control of the disease is based currently on identification of EIAV inapparent carriers by laboratory tests. Recombinant envelope protein (rgp90) was expressed in Escherichia coli and evaluated via enzyme-linked immunosorbent assay (ELISA). There was an excellent agreement (95.42%) between the ELISA results using rgp90 and agar gel immunodiffusion test results. AGID is considered the "gold-standard" serologic test for equine infectious anemia (EIA). After 1160 serum samples were tested, the relative sensitivity and specificity of the ELISA were 96.1% and 96.4%, respectively. Moreover, analysis diagnostic accuracy of the ELISA was performed. The ELISA proved robust. Furthermore, good reproducibility was observed for the negative controls and, positive controls for all plates tested.


Subject(s)
Antibodies, Viral/blood , Equine Infectious Anemia/diagnosis , Gene Products, env , Infectious Anemia Virus, Equine/immunology , Recombinant Proteins , Agar , Animals , Antigens, Viral/genetics , Antigens, Viral/immunology , Antigens, Viral/metabolism , Enzyme-Linked Immunosorbent Assay , Gene Products, env/genetics , Gene Products, env/immunology , Gene Products, env/metabolism , Horses , Immunodiffusion , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Recombinant Proteins/metabolism , Reproducibility of Results , Sensitivity and Specificity
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