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Hendrickson, H. L.

Publications and source records attributed to Hendrickson, H. L..

3 recordsLinked to original sources

In Vitro Evolution to Increase the Titers of Difficult Bacteriophages: Rapid Appelmans Protocol

Bacteriophages are becoming increasingly important in the race to find alternatives to antibiotics. Unfortunately, bacteriophages that might otherwise be useful are sometimes discarded due to low titers making them unsuitable for downstream applications. Here, we present two distinct approaches to experimentally evolve novel New Zealand Paenibacillus larvae bacteriophages. The first approach uses the traditional agar-overlay method, whereas the other was a Rapid Appelmans Protocol (RAP) modelled after the established Appelmans Method. Both approaches resulted in an increase in plaque-forming units (PFU/mL). The RAP approach was significantly faster and simpler, and allowed us to evolve a set of bacteriophages in as little as four days, increasing titers 100-1000-fold relative to their ancestors. The resultant titers were sufficient to extract and sequence DNA from these bacteriophages. An analysis of these phage genomes is provided. We also propose a model that describes the parameters that allow the RAP approach to select improvement of bacteriophage titer. The RAP approach is an effective method for experimentally evolving previously intractable bacteriophages in a high-throughput and expeditious manner.

microbiology↗

Protozoan predation drives adaptive divergence in Pseudomonas fluorescens SBW25; ecology meets experimental evolution.

Protozoan predators can affect the structure of bacterial communities, but investigations of how predation might influence bacterial evolution and antagonistic behaviours are scarce. Here, we performed a 20-day predator-prey evolution experiment on solid media to investigate the effect of continuous protozoan predation on bacterial traits using Pseudomonas fluorescens SBW25 as prey and Naegleria gruberi as an amoeboid predator. We observed the divergence of colony morphotypes coincident with an increase in bacterial grazing resistance and relative prey fitness in selected bacterial isolates. When subjected to these resistant prey, N. gruberi show reduced activity (increased encystment) and limited replication. An investigation of the mutations responsible for predation resistance reveals mutations in wspF and amrZ genes, affecting biofilm formation and motility. The bacterial mutants in the wspF gene successfully colonise the air-liquid interface and produce robust cellulose biofilms that prevent predation. The mutation in the amrZ mutant withstands predation but this variant produces low levels of cellulose and limited swarming motility. Our findings suggest that protozoan predation can profoundly influence the course of genetic and phenotypic evolution in a short period.

evolutionary biology↗

Experimental Evolution of Cell Shape in Bacteria

Maintenance of rod-shape in bacterial cells depends on the actin-like protein MreB. Deletion of mreB from Pseudomonas fluorescens SBW25 results in viable spherical cells of variable volume and reduced fitness. Using a combination of time-resolved microscopy and biochemical assay of peptidoglycan synthesis, we show that reduced fitness is a consequence of perturbed cell size homeostasis that arises primarily from differential growth of daughter cells. A 1,000-generation selection experiment resulted in rapid restoration of fitness with derived cells retaining spherical shape. Mutations in the peptidoglycan synthesis protein Pbp1A were identified as the main route for evolutionary rescue with genetic reconstructions demonstrating causality. Compensatory pbp1A mutations that targeted transpeptidase activity enhanced homogeneity of cell wall synthesis on lateral surfaces and restored cell size homeostasis. Mechanistic explanations require enhanced understanding of why deletion of mreB causes heterogeneity in cell wall synthesis. We conclude by presenting two testable hypotheses, one of which posits that heterogeneity stems from non-functional cell wall synthesis machinery, while the second posits that the machinery is functional, albeit stalled. Overall, our data provide support for the second hypothesis and draw attention to the importance of balance between transpeptidase and glycosyltransferase functions of peptidoglycan building enzymes for cell shape determination.

microbiology↗