Laboratoire de Physique de l'ENS, Université Paris Cité, Ecole normale supérieure, UniversitéPSL, Sorbonne Université, CNRS, 75005 Paris, Paris, France; Institut de biologie de l’Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Research University, Paris, France; Université Paris Cité, Paris, France
Monica L Gerth
New Zealand Institute for Advanced Study, Massey University, Auckland, New Zealand
Barbara Ritzl-Rinkenberger
Department of Molecular Biology, Umeå University, Umeå, Sweden; Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, SciLifeLab, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden
Andrew D Farr
Department of Microbial Population Biology, Max Planck Institute for Evolutionary Biology, Plön, Germany
Yunhao Liu
New Zealand Institute for Advanced Study, Massey University, Auckland, New Zealand
Xue-Xian Zhang
Institute of Natural and Mathematical Science, Massey University, Auckland, New Zealand
Michael Miller
Institute of Natural and Mathematical Science, Massey University, Auckland, New Zealand
Department of Molecular Biology, Umeå University, Umeå, Sweden; Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, SciLifeLab, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden
New Zealand Institute for Advanced Study, Massey University, Auckland, New Zealand; Department of Microbial Population Biology, Max Planck Institute for Evolutionary Biology, Plön, Germany; Laboratoire Biophysique et Évolution, CBI, ESPCI Paris, Université PSL, Paris, France
Institute of Natural and Mathematical Science, Massey University, Auckland, New Zealand; School of Biological Sciences, University of Canterbury, Christchurch, New Zealand
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 1000-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.