Premium
HpaB from Xanthomonas campestris pv. vesicatoria acts as an exit control protein in type III‐dependent protein secretion
Author(s) -
Büttner Daniela,
Gürlebeck Doreen,
Noël Laurent D.,
Bonas Ulla
Publication year - 2004
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2004.04302.x
Subject(s) - effector , xanthomonas campestris , biology , secretion , chaperone (clinical) , biochemistry , mutant , xanthomonas , transport protein , gene , medicine , pathology
Summary The hrp (hypersensitive response and pathogenicity) gene cluster of the plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria encodes a type III secretion (TTS) system, which injects bacterial effector proteins into the plant cell. Here, we characterized hpaB ( hpa, hrp ‐associated), which encodes a pathogenicity factor with typical features of a TTS chaperone. We show that HpaB is important for the efficient secretion of at least five effector proteins but is dispensable for the secretion of non‐effectors such as XopA and the TTS translocon protein HrpF. GST pull‐down assays revealed that HpaB interacts with two unrelated effector proteins, AvrBs1 and AvrBs3, but not with XopA. The HpaB‐binding site is located within the first 50 amino acids of AvrBs3. This region also contains the targeting signal for HpaB‐dependent secretion, which is missing in HrpF and XopA. Intriguingly, the N‐termini of HrpF and XopA target the AvrBs3Δ2 reporter for translocation in a Δ hpaB mutant but not in the wild‐type strain. This indicates that HpaB plays an essential role in the exit control of the TTS system. Our data suggest that HpaB promotes the secretion of a large set of effector proteins and prevents the delivery of non‐effectors into the plant cell.