Virulence-Associated Adhesins
Virulence-associated antigens involved in adhesin have been identified in several organisms: Haemophilus influenzae biogroup aegyptius; Escherichia coli K 1 ; EHEC E.coli; Actinobacillus actinomycetencomitans; Haemophilus somnus; Haemophilus ducreyi; EPEC E.coli; EA EC E.coli; uropathogenic E.coli; Shigella flexneri; Brucella melitensis; Brucella suis; Ralstonia solanacearum; Sinorhizobium meliloti; Bradorhizobium japonicum; and Burkholderia fungorum. Although the degree of sequence identity between the adhesins is low, they share a common arrangement of domains from N-terminus to C-terminus, namely: a leader peptide; a globular head; a coiled-coil region; and a transmembrane anchor region.
1 . A polypeptide comprising one or more of: (a) an amino acid sequence selected from the group consisting of SEQ ID NOS: 51, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, and 54; (b) an amino acid sequence having at least 70% identity to a sequence as defined in (a); and/or (c) an amino acid sequence comprising a fragment of at least 8 consecutive amino acids of a sequence as defined in (a).
2 . The polypeptide of claim 1 , wherein the fragment of (c) does not include one or more of four domains of the sequence of (a).
3 . The polypeptide of claim 1 , wherein the fragment of (c) includes at least one complete domain of the sequence of (a).
4 . The polypeptide of claim 1 , in oligomeric form.
5 . A polypeptide of the formula NH2 A-{-X-L-}X-B—COOH, wherein: X comprises an amino acid sequence: (a) having at least 70% identity to one or more of SEQ ID NOS: 1-18, 51 or 54; and/or (b) which is a fragment of at least 8 consecutive amino acids of one or more of SEQ ID NOS: 1-18, 51 or 54; L is an optional linker amino acid sequence; A is an optional N terminal amino acid sequence; B is an optional C terminal amino acid sequence; and x is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20.
6 . A polypeptide comprising the amino acid sequence -A-W 1 —W 2 —W 3 —W 4 —B—, wherein:
A is an optional N-terminus sequence;
B is an optional C-terminus sequence;
W 1 is an optional amino acid sequence: (a) having at least 70% identity to the leader peptide of one or more of SEQ ID NOS: 1-18 or 51; and/or (b) which is a fragment of at least 8 consecutive amino acids of the leader peptide of one or more of SEQ ID NOS: 1-18 or 51; W 2 is an optional amino acid sequence: (a) having at least 70% identity to the globular head of one or more of SEQ ID NOS: 1-18 or 51; and/or (b) which is a fragment of at least 8 consecutive amino acids of the leader peptide of one or more of SEQ ID NOS: 1-18 or 51; W 3 is an optional amino acid sequence: (a) having at least 70% identity to the coiled-coil domain of one or more of SEQ ID NOS: 1-18 or 51; and/or (b) which is a fragment of at least 8 consecutive amino acids of the leader peptide of one or more of SEQ ID NOS: 1-18 or 51; W 4 is an optional amino acid sequence: (a) having at least 70% identity to the transmembrane anchor region of one or more of SEQ ID NOS: 1-18 or 51; and/or (b) which is a fragment of at least 8 consecutive amino acids of the leader peptide of one or more of SEQ ID NOS: 1-18 or 51;
provided that at least one of W 1 , W 2 , W 3 or W 4 is present.
7 . An adhesin from Haemophilus aeyptius, wherein the adhesin comprises: (a) amino acid sequence SEQ ID NO: 52; (b) an amino acid sequence having at least 70% identity to SEQ ID NO: 52, and/or (c) an amino acid sequence which is a fragment of at least 8 consecutive amino acids of SEQ ID NO: 52.
8 . An antibody that binds to the polypeptide of claim 1 .
9 . Nucleic acid encoding the polypeptide of claim 1 .
10 . A pharmaceutical composition comprising the polypeptide of claim 1 .
11 . (canceled)
12 . (canceled)
13 . A method for raising an immune response in a mammal comprising the step of administering an effective amount of the composition of claim 10 to said mammal.
14 . Nucleic acid encoding the antibody of claim 8 .
15 . A pharmaceutical composition comprising the antibody of claim 8 .
16 . A pharmaceutical composition comprising the nucleic acid of claim 9 .
17 . A pharmaceutical composition comprising the nucleic acid of claim 14 .
18 . A pharmaceutical composition comprising the polypeptide of claim 5 .
19 . A pharmaceutical composition comprising the polypeptide of claim 6 .
20 . A pharmaceutical composition comprising the polypeptide of claim 7 .
21 . A method for raising an immune response in a mammal comprising the step of administering an effective amount of the composition of claim 18 to said mammal.
22 . A method for raising an immune response in a mammal comprising the step of administering an effective amount of the composition of claim 19 to said mammal.
23 . A method for raising an immune response in a mammal comprising the step of administering an effective amount of the composition of claim 20 to said mammal.