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Updated: Jun 7, 2026

Defining Substrate Specificities for Lipase and Phospholipase Candidates
Published on: November 23, 2016
Phospholipase D promotes Arcanobacterium haemolyticum adhesion via lipid raft remodeling and host cell death
Erynn A Lucas1, Stephen J Billington, Petteri Carlson
1Department of Veterinary Science and Microbiology, The University of Arizona, Tucson, AZ 85721, USA.
Background:
Arcanobacterium haemolyticum is an emerging bacterial pathogen, causing pharyngitis and more invasive infections. This organism expresses an unusual phospholipase D (PLD), which we propose promotes bacterial pathogenesis through its action on host cell membranes. The pld gene is found on a genomic region of reduced %G + C, suggesting recent horizontal acquisition.
Results:
Recombinant PLD rearranged HeLa cell lipid rafts in a dose-dependent manner and this was inhibited by cholesterol sequestration. PLD also promoted host cell adhesion, as a pld mutant had a 60.3% reduction in its ability to adhere to HeLa cells as compared to the wild type. Conversely, the pld mutant appeared to invade HeLa cells approximately two-fold more efficiently as the wild type. This finding was attributable to a significant loss of host cell viability following secretion of PLD from intracellular bacteria. As determined by viability assay, only 15.6% and 82.3% of HeLa cells remained viable following invasion by the wild type or pld mutant, respectively, as compared to untreated HeLa cells. Transmission electron microscopy of HeLa cells inoculated with A. haemolyticum strains revealed that the pld mutant was contained within intracellular vacuoles, as compared to the wild type, which escaped the vacuole. Wild type-infected HeLa cells also displayed the hallmarks of necrosis. Similarly inoculated HeLa cells displayed no signs of apoptosis, as measured by induction of caspase 3/7, 8 or 9 activities.
Conclusions:
These data indicate that PLD enhances bacterial adhesion and promotes host cell necrosis following invasion, and therefore, may be important in the disease pathogenesis of A. haemolyticum infections.
Insights
Arcanobacterium haemolyticum phospholipase D (PLD) enhances bacterial adhesion and causes host cell necrosis, contributing to disease pathogenesis. This enzyme rearranges cell membranes, aiding bacterial invasion and survival.
Area of Science:
- Microbiology
- Pathogenesis
- Bacterial Virulence Factors
Background:
- Arcanobacterium haemolyticum is an emerging pathogen causing pharyngitis and invasive infections.
- The bacterium possesses an unusual phospholipase D (PLD) enzyme, potentially key to its virulence.
- The pld gene's genomic location suggests recent horizontal gene transfer.
Purpose of the Study:
- To investigate the role of Arcanobacterium haemolyticum phospholipase D (PLD) in bacterial pathogenesis.
- To elucidate the mechanisms by which PLD affects host cell membranes and bacterial-host interactions.
Main Methods:
- Recombinant PLD was used to assess its effect on HeLa cell lipid rafts.
- Adhesion and invasion assays were performed using wild-type and pld mutant strains of A. haemolyticum.
- Cell viability, intracellular vacuole escape, and apoptosis/necrosis markers were analyzed.
Main Results:
- Recombinant PLD disrupted HeLa cell lipid rafts in a dose-dependent manner.
- A pld mutant showed significantly reduced adhesion (60.3%) but increased invasion (two-fold) compared to wild-type.
- Wild-type A. haemolyticum caused significant host cell necrosis and vacuole escape, unlike the pld mutant.
Conclusions:
- PLD enhances bacterial adhesion to host cells.
- PLD promotes host cell necrosis following invasion, indicating its importance in A. haemolyticum pathogenesis.
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