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Updated: Jun 13, 2026

Biomimetic Materials to Characterize Bacteria-host Interactions
Published on: November 16, 2015
Photorhabdus adhesion modification protein (Pam) binds extracellular polysaccharide and alters bacterial attachment
Robert T Jones1, Maria Sanchez-Contreras, Isabella Vlisidou
1Department of Biology and Biochemistry, University of Bath, Claverton Down, Bath BA27AY, UK.
Background:
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.
Insights
Photorhabdus asymbiotica secretes a temperature-dependent protein, Pam, that enhances bacterial surface attachment in insects. Despite its abundance and conservation, Pam does not impact virulence or symbiosis.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Photorhabdus bacteria are Gram-negative, symbiotic, and insect-pathogenic.
- Photorhabdus asymbiotica infects both insects and humans.
- Investigated secreted proteome of P. asymbiotica at different temperatures to identify host-relevant proteins.
Purpose of the Study:
- Identify proteins secreted by P. asymbiotica at insect (28°C) and human (37°C) temperatures.
- Characterize a novel, temperature-dependent secreted protein, designated Pam.
- Determine the role of Pam in bacterial interactions with hosts and surfaces.
Main Methods:
- Comparative secretome analysis at different temperatures.
- Gene sequencing and protein characterization.
- Insect bioassays (injection and feeding).
- Surface Plasmon Resonance (SPR) for binding studies.
- Genetic knockout of the pam gene.
Main Results:
- Identified Pam, a small, abundant protein secreted only at 28°C.
- Pam gene is conserved across the Photorhabdus genus.
- Pam enhances bacterial surface attachment and is associated with extracellular polysaccharide (EPS).
- Pam exhibits adhesive properties but lacks insecticidal activity.
- Pam knockout did not affect insect virulence or nematode symbiosis.
Conclusions:
- Pam is a temperature-dependent secreted protein in P. asymbiotica.
- Pam enhances bacterial surface attachment in insect hemolymph, likely via EPS modification.
- Despite conservation and abundance, Pam is not essential for virulence or symbiosis.
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