Immunoreactive protein orthologs of Ehrlichia canis and E. chaffeensis

US9645148B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9645148-B2
Application numberUS-201514818221-A
CountryUS
Kind codeB2
Filing dateAug 4, 2015
Priority dateJun 16, 2005
Publication dateMay 9, 2017
Grant dateMay 9, 2017

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Abstract

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The present invention concerns gp36 immunoreactive compositions for E. canis and gp 47 immunoreactive compositions for E. chaffeensis . In particular, epitopes for E. canis gp36 and E. chaffeensis gp 47 are disclosed. In certain embodiments, the immunoreactive compositions comprise tandem repeats having carbohydrate moieties.

First claim

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What is claimed is: 1. A method of identifying an E. canis or E. chaffeensis infection using a sample from an individual suspected of having such an infection, comprising assaying the sample for an antibody that immunologically binds a polypeptide consisting of: (a) a sequence selected from the group consisting of SEQ ID NO:45 and SEQ ID NO:22; or (b) a sequence selected from the group consisting of SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:23 and SEQ ID NO:24 wherein the sample is assayed by means of an immunoassay in which antibodies from the sample, if present, will bind to an immobilized polypeptide comprising a sequence at least 90% identical to the sequence of (a) or (b), and further wherein bound antibodies are detected by means of a detectable label. 2. The method of claim 1 , wherein the immunoassay is a enzyme linked immunosorbent assay (ELISA), radioimmunoassay (RIA), immunoradiometric assay, fluoroimmunoassay, chemiluminescent assay, bioluminescent assay, or a Western blot. 3. The method of claim 1 , wherein the sample is assayed by contacting an immobilized polypeptide comprising a sequence selected from the group consisting of SEQ ID NO:45 and SEQ ID NO:22, with said sample and detecting immunological binding of the antibody thereto. 4. The method of claim 1 , wherein the sample is assayed by contacting an immobilized polypeptide comprising SEQ ID NO: 22, with said sample and detecting immunological binding of the antibody thereto. 5. The method of claim 1 , wherein the sample is assayed by contacting an immobilized polypeptide comprising a sequence selected from the group consisting of SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:23 and SEQ ID NO:24, with said sample and detecting immunological binding of the antibody thereto. 6. The method of claim 1 , wherein the sample is assayed by contacting an immobilized polypeptide comprising SEQ ID NO:23 or SEQ ID NO:24, with said sample and detecting immunological binding of the antibody thereto. 7. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:45. 8. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:25. 9. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:26. 10. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:27. 11. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:28. 12. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:23. 13. The method of claim 1 , wherein the immobilized polypeptide comprises SEQ ID NO:24.

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What does patent US9645148B2 cover?
The present invention concerns gp36 immunoreactive compositions for E. canis and gp 47 immunoreactive compositions for E. chaffeensis . In particular, epitopes for E. canis gp36 and E. chaffeensis gp 47 are disclosed. In certain embodiments, the immunoreactive compositions comprise tandem repeats having carbohydrate moieties.
Who is the assignee on this patent?
Res Dev Foundation
What technology area does this patent fall under?
Primary CPC classification G01N33/56911. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue May 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).