M. Day, Arin C Esterbrook, Ignatius Bisharat, Abdullah Saleh Albqomi, Bryn C. Kennell, Russ Manteca, Heaton Oakes, Geoffrey M. Scalarone, G. Scalarone
{"title":"Comparison of Two Enzyme Immunoassays and Four Lysate Antigens for the Detection of Antibody in Canine Blastomycosis","authors":"M. Day, Arin C Esterbrook, Ignatius Bisharat, Abdullah Saleh Albqomi, Bryn C. Kennell, Russ Manteca, Heaton Oakes, Geoffrey M. Scalarone, G. Scalarone","doi":"10.4236/OJVM.2021.114009","DOIUrl":null,"url":null,"abstract":"Blastomycosis, \nthe systemic fungal disease of humans and animals caused by Blastomyces \ndermatitidis and the cryptic species Blastomyces gilchristii, is often misdiagnosed as a \nbacterial or viral pulmonary disease. Therefore, the development of improved \nimmunodiagnostic assays for this disease has been the primary focus of research \nin our laboratory. The present study was designed to evaluate four Blastomyces yeast-phase lysate \nantigenic preparations (human, 597, Eagle River, WI; dog, ERC-2, WI; Human, \nB5927, Mountain Iron, MN; soil, 85, Georgia, ATCC 56920) for their ability to \ndetect antibody in 48 serum specimens from dogs with diagnosed blastomycosis \nusing an indirect ELISA (STD) compared to a biotin-streptavidin ELISA (B-SA). \nAll four lysate antigens were able to detect antibodies in the specimens with mean absorbance values \nranging from 0.930 (B5927) to 1.142 (ERC-2) with the STD ELSA and from 1.395 \n(B5927) to 1.775 (85) with the B-SA ELISA. The results indicated that both \nELISA methods could be utilized for antibody detection, but the B-SA ELISA \nexhibited greater sensitivity than the STD ELISA with all four of the lysates.","PeriodicalId":61886,"journal":{"name":"兽医学(英文)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"兽医学(英文)","FirstCategoryId":"1091","ListUrlMain":"https://doi.org/10.4236/OJVM.2021.114009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Blastomycosis,
the systemic fungal disease of humans and animals caused by Blastomyces
dermatitidis and the cryptic species Blastomyces gilchristii, is often misdiagnosed as a
bacterial or viral pulmonary disease. Therefore, the development of improved
immunodiagnostic assays for this disease has been the primary focus of research
in our laboratory. The present study was designed to evaluate four Blastomyces yeast-phase lysate
antigenic preparations (human, 597, Eagle River, WI; dog, ERC-2, WI; Human,
B5927, Mountain Iron, MN; soil, 85, Georgia, ATCC 56920) for their ability to
detect antibody in 48 serum specimens from dogs with diagnosed blastomycosis
using an indirect ELISA (STD) compared to a biotin-streptavidin ELISA (B-SA).
All four lysate antigens were able to detect antibodies in the specimens with mean absorbance values
ranging from 0.930 (B5927) to 1.142 (ERC-2) with the STD ELSA and from 1.395
(B5927) to 1.775 (85) with the B-SA ELISA. The results indicated that both
ELISA methods could be utilized for antibody detection, but the B-SA ELISA
exhibited greater sensitivity than the STD ELISA with all four of the lysates.