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dc.contributor.authorJones, RT
dc.contributor.authorSanchez-Contreras, M
dc.contributor.authorVlisidou, I
dc.contributor.authorAmos, MR
dc.contributor.authorYang, G
dc.contributor.authorMuñoz-Berbel, X
dc.contributor.authorUpadhyay, A
dc.contributor.authorPotter, UJ
dc.contributor.authorJoyce, SA
dc.contributor.authorCiche, TA
dc.contributor.authorJenkins, AT
dc.contributor.authorBagby, S
dc.contributor.authorffrench-Constant, Richard
dc.contributor.authorWaterfield, NR
dc.date.accessioned2016-02-02T15:11:44Z
dc.date.issued2010-05-12
dc.description.abstractBACKGROUND: Photorhabdus are Gram-negative nematode-symbiotic and insect-pathogenic bacteria. The species Photorhabdus asymbiotica is able to infect humans as well as insects. We investigated the secreted proteome of a clinical isolate of P. asymbiotica at different temperatures in order to identify proteins relevant to the infection of the two different hosts. RESULTS: A comparison of the proteins secreted by a clinical isolate of P. asymbiotica at simulated insect (28 degrees C) and human (37 degrees C) temperatures led to the identification of a small and highly abundant protein, designated Pam, that is only secreted at the lower temperature. The pam gene is present in all Photorhabdus strains tested and shows a high level of conservation across the whole genus, suggesting it is both ancestral to the genus and probably important to the biology of the bacterium. The Pam protein shows limited sequence similarity to the 13.6 kDa component of a binary toxin of Bacillus thuringiensis. Nevertheless, injection or feeding of heterologously produced Pam showed no insecticidal activity to either Galleria mellonella or Manduca sexta larvae. In bacterial colonies, Pam is associated with an extracellular polysaccharide (EPS)-like matrix, and modifies the ability of wild-type cells to attach to an artificial surface. Interestingly, Surface Plasmon Resonance (SPR) binding studies revealed that the Pam protein itself has adhesive properties. Although Pam is produced throughout insect infection, genetic knockout does not affect either insect virulence or the ability of P. luminescens to form a symbiotic association with its host nematode, Heterorhabditis bacteriophora. CONCLUSIONS: We studied a highly abundant protein, Pam, which is secreted in a temperature-dependent manner in P. asymbiotica. Our findings indicate that Pam plays an important role in enhancing surface attachment in insect blood. Its association with exopolysaccharide suggests it may exert its effect through mediation of EPS properties. Despite its abundance and conservation in the genus, we find no evidence for a role of Pam in either virulence or symbiosis.en_GB
dc.description.sponsorshipBBSRCen_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.description.sponsorshipEMBEK1en_GB
dc.identifier.citationVol. 10, pp. 141 -en_GB
dc.identifier.doi10.1186/1471-2180-10-141
dc.identifier.grantnumberBB/E021328/1en_GB
dc.identifier.grantnumber076124en_GB
dc.identifier.grantnumber211436; EU- FP7en_GB
dc.identifier.other1471-2180-10-141
dc.identifier.urihttp://hdl.handle.net/10871/19547
dc.language.isoenen_GB
dc.publisherBioMed Centralen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/20462430en_GB
dc.relation.urlhttp://bmcmicrobiol.biomedcentral.com/articles/10.1186/1471-2180-10-141en_GB
dc.rightsCopyright © 2010 Jones et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectAdhesins, Bacterialen_GB
dc.subjectAnimalsen_GB
dc.subjectBacillus thuringiensisen_GB
dc.subjectBacterial Adhesionen_GB
dc.subjectBacterial Proteinsen_GB
dc.subjectBacterial Toxinsen_GB
dc.subjectElectrophoresis, Gel, Two-Dimensionalen_GB
dc.subjectGram-Negative Bacterial Infectionsen_GB
dc.subjectHumansen_GB
dc.subjectLepidopteraen_GB
dc.subjectNematodaen_GB
dc.subjectPhotorhabdusen_GB
dc.subjectPolysaccharides, Bacterialen_GB
dc.subjectProteomeen_GB
dc.subjectSequence Homology, Amino Aciden_GB
dc.subjectSurface Plasmon Resonanceen_GB
dc.subjectSymbiosisen_GB
dc.subjectTemperatureen_GB
dc.subjectVirulenceen_GB
dc.titlePhotorhabdus adhesion modification protein (Pam) binds extracellular polysaccharide and alters bacterial attachment.en_GB
dc.typeArticleen_GB
dc.date.available2016-02-02T15:11:44Z
dc.identifier.issn1471-2180
exeter.place-of-publicationEngland
dc.descriptionJournal Articleen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.identifier.journalBMC Microbiologyen_GB


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