Characterization of three novel genetic loci encoding bacteriocins associated with Xanthomonas perforans.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
23
01
2020
accepted:
02
05
2020
entrez:
30
5
2020
pubmed:
30
5
2020
medline:
12
8
2020
Statut:
epublish
Résumé
Bacterial spot is a destructive disease of tomato in Florida that prior to the early 1990s was caused by Xanthomonas euvesicatoria. X. perforans was first identified in Florida in 1991 and by 2006 was the only xanthomonad associated with bacterial spot disease in tomato. The ability of an X. perforans strain to outcompete X. euvesicatoria both in vitro and in vivo was at least in part associated with the production of three bacteriocins designated Bcn-A, Bcn-B, and Bcn-C. The objective of this study was to characterize the genetic determinants of these bacteriocins. Bcn-A activity was confined to one locus consisting of five ORFs of which three (ORFA, ORF2 and ORF4) were required for bacteriocin activity. The fifth ORF is predicted to encode an immunity protein to Bcn-A based on in vitro and in vivo assays. The first ORF encodes Bcn-A, a 1,398 amino acid protein, which bioinformatic analysis predicts to be a member of the RHS family of toxins. Based on results of homology modeling, we hypothesize that the amino terminus of Bcn-A interacts with a protein in the outer membrane of X. euvesicatoria. The carboxy terminus of the protein may interact with an as yet unknown protein(s) and puncture the X. euvesicatoria membrane, thereby delivering the accessory proteins into the target and causing cell death. Bcn-A appears to be activated upon secretion based on cell fractionation assays. The other two loci were each shown to be single ORFs encoding Bcn-B and Bcn-C. Both gene products possess homology toward known proteases. Proteinase activity for both Bcn-B and Bcn-C was confirmed using a milk agar assay. Bcn-B is predicted to be an ArgC-like serine protease, which was confirmed by PMSF inhibition of proteolytic activity, whereas Bcn-C has greater than 50% amino acid sequence identity to two zinc metalloproteases.
Identifiants
pubmed: 32469926
doi: 10.1371/journal.pone.0233301
pii: PONE-D-20-02156
pmc: PMC7259588
doi:
Substances chimiques
Bacterial Proteins
0
Bacteriocins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0233301Subventions
Organisme : NCRR NIH HHS
ID : P20 RR016461
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM103499
Pays : United States
Déclaration de conflit d'intérêts
We also declare no competing interests in the research. Dr. Aaron Hert, currently affiliated with a commercial enterprise, was involved in the research during his affiliation with University of Florida as a graduate student. The commercial affiliation does not alter our adherence to PLOS ONE policies on sharing data and materials.
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