2020
DOI: 10.1111/vcp.12908
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Canonical correlative analyses among an enzyme‐linked immunosorbent assay using synthetic peptides, an indirect fluorescent antibody test, and hematologic measurements in dogs infected with Ehrlichia canis

Abstract: BackgroundImmunoreactive tandem repeat proteins (TRPs) in amino acid sequences were identified and employed in the serologic diagnosis of canine monocytic ehrlichiosis (CME).ObjectivesThis study evaluated using TRP19 and TRP36 synthetic protein antigens with enzyme‐linked immunosorbent assays (ELISAs) and compared the results with an indirect fluorescent antibody test (IFAT) to diagnose CME in the serum of dogs with suspected CME.MethodsThe sera of 243 dogs that exhibited clinical and hematologic signs suggest… Show more

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Cited by 7 publications
(18 citation statements)
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References 27 publications
(46 reference statements)
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“…Complete clinical data of the dogs in this study were not available for reasons of medical confidentiality. No clinical differences between US or Br genotypes were observed in a hospital population of dogs suffering from CME in an endemic area in Brazil [ 5 ], while clinical differences were observed in dogs infected by different genotypes in another study [ 18 ]. To date, the genetic diversity may be related to the host–pathogen relationship.…”
Section: Discussionmentioning
confidence: 99%
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“…Complete clinical data of the dogs in this study were not available for reasons of medical confidentiality. No clinical differences between US or Br genotypes were observed in a hospital population of dogs suffering from CME in an endemic area in Brazil [ 5 ], while clinical differences were observed in dogs infected by different genotypes in another study [ 18 ]. To date, the genetic diversity may be related to the host–pathogen relationship.…”
Section: Discussionmentioning
confidence: 99%
“…ELISA was performed with synthetic peptides corresponding to epitopes from E. canis TRP19 (HFTGPTSFEVNLSEEEKMELQEVS) [ 7 ], USTRP36 (TEDSVSAPATEDSVSAPA) [ 3 ], BrTRP36 (ASVVPEAEASVVPEAEASVVPEAE) [ 4 ] and CRTRP36 (EASVVPAAEAPQPAQQTEDEFFSDGIEA) [ 11 ]. All the ELISA assays were performed according to a previously described protocol [ 4 , 5 ]. Differences between the results found per region and E. canis TRP36 peptides were evaluated by the chi-square test and p ≤ 0.05 was considered significant.…”
Section: Methodsmentioning
confidence: 99%
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“…ELISA was performed with synthetic peptides corresponding to epitopes from E. canis TRP19 (HFTGPTSFEVNLSEEEKMELQEVS) [7], USTRP36 (TEDSVSAPATEDSVSAPA) [3], BrTRP36 (ASVVPEAEASVVPEAEASVVPEAE) [4] and CRTRP36 (EASVVPAAEAPQPAQQTEDEFFSDGIEA) [11]. All the ELISA assays were performed according to the protocol described [4][5]. Differences between results found per region and E. canis TRP36 peptides were evaluated by the chi-square test and p≤0.05 was considered significant.…”
Section: Methodsmentioning
confidence: 99%
“…TRP19 is highly conserved among the known E. canis strains. It is a specific target for serological diagnostics [3][4][5][6] and a strong candidate for vaccine antigen for CME, due to its high degree of conservation and because it is a component of the morula membrane [7].…”
Section: Introductionmentioning
confidence: 99%