Microbiome identification and bacteriophage formulations
US-2024123002-A1 · Apr 18, 2024 · US
US2017205407A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017205407-A1 |
| Application number | US-201615019520-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 9, 2016 |
| Priority date | Aug 28, 2009 |
| Publication date | Jul 20, 2017 |
| Grant date | — |
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Chimera proteins including: (i) at least one sequence of a DbpA protein of a Borrelia species selected from B. afzelii, B. burgdorferi sensu stricto and B. garinii , and (ii) at least one sequence of an OspC protein of a Borrelia species selected from B. afzelii, B. burgdorferi sensu stricto and B. garinii . Also, a method and a kit for the in vitro diagnosis of Lyme borreliosis using said proteins.
Opening claim text (preview).
1 . A polypeptide comprising (i) a Decorin-binding protein A (DbpA) extracellular domain portion from B. afzelii, B. burgdorferi sensu stricto , or B. garinii that includes DbpA immunodominant epitope regions, and (ii) an Outer-surface protein C (OspC) extracellular domain portion from B. afzelii, B. burgdorferi sensu stricto , or B. garinii that includes OspC immunodominant epitope regions. 2 . The polypeptide as claimed in claim 1 , wherein the DbpA extracellular domain portion is on the N-terminal side of the polypeptide, and the OspC extracellular domain portion is on the C-terminal side of the polypeptide. 3 . The polypeptide as claimed in claim 1 , further comprising a linking region between the DbpA extracellular domain portion and the OspC extracellular domain portion. 4 . A polypeptide comprising (i) a first amino acid sequence having at least 40% sequence identity with any of the amino acid sequences selected from the group consisting of SEQ ID NOs: 1, 3, 5, and 6, and (ii) a second amino acid sequence having at least 50% sequence identity with any of the amino acid sequences selected from the group consisting of SEQ ID NOs: 2, 4, and 7. 5 . The polypeptide as claimed in claim 4 , wherein the first amino acid sequence is on the N-terminal side of the polypeptide, and the second amino acid sequence is on the C-terminal side of the polypeptide. 6 . The polypeptide as claimed in claim 4 , further comprising a linking region between the first amino acid sequence and the second amino acid sequence. 7 . The polypeptide as claimed in claim 4 , further comprising a third amino acid sequence of at least 6 contiguous histidines at the N-terminal or C-terminal end. 8 . The polypeptide as claimed in claim 4 , wherein the first amino acid sequence comprises any of the amino acid sequences of SEQ ID NOs: 1, 3, 5, or 6, and the second amino acid sequence comprises any of the amino acid sequences of SEQ ID NOs: 2, 4, or 7. 9 . The polypeptide as claimed in claim 4 , comprising the amino acid sequences of SEQ ID NO: 1 and SEQ ID NO: 2. 10 . The polypeptide as claimed in claim 4 , comprising the amino acid sequences of SEQ ID NO: 3 and SEQ ID NO: 4. 11 . The polypeptide as claimed in claim 4 , comprising the amino acid sequences of SEQ ID NO: 5 and SEQ ID NO: 7. 12 . The polypeptide as claimed in claim 4 , comprising the amino acid sequences of SEQ ID NO: 6 and SEQ ID NO: 7. 13 . The polypeptide as claimed in claim 4 , comprising the amino acid sequences of SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 7. 14 . A nucleic acid encoding the polypeptide as claimed in claim 4 . 15 . A diagnostic kit comprising the polypeptide as claimed in claim 1 . 16 . The diagnostic kit as claimed in claim 15 , further comprising an anti-human-immunoglobulin labeled with a label. 17 . The diagnostic kit as claimed in claim 15 , further comprising a chimeric VlsE polypeptide. 18 . A method for the in vitro diagnosis of Lyme borreliosis using a biological sample, comprising: bringing the biological sample into contact with at least one polypeptide as claimed in claim 1 ; and determining whether there is formation of an immunological complex between the polypeptide and antibodies of the biological sample. 19 . The method as claimed in claim 18 , wherein formation of the immunological complex is determined by adding at least one anti-human-immunoglobulin labeled with a label. 20 . The method as claimed in claim 18 , wherein the polypeptide is immobilized on a solid support.
Immunostimulants · CPC title
Detection of antibodies in sample from host which are directed against antigens from microorganisms · CPC title
Bacteria · CPC title
from bacteria · CPC title
from Spirochaetales (O), e.g. Treponema, Leptospira · CPC title
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