
Manuel Campos
Laboratoire de Microbiologie et Génétique Moléculaires (LMGM), Centre de Biologie Intégrative (CBI), Centre National de la Recherche Scientifique (CNRS), 31062 Toulouse, France; Université de Toulouse, Université Paul Sabatier, 31062 Toulouse, France
Dr. Manuel Campos was trained as a molecular geneticist and cellular biologist. After completing a PhD in France on the helicoidal structure of a bacterial pilus-like structure, he moved to Christine Jacobs-Wagner’s lab to study cell size homeostasis in bacteria. He currently holds a permanent researcher position at the CNRS in Toulouse, France. He currently investigates the mechanisms underpinning the coordination between the division and DNA cycles in Escherichia coli through a comparative cell biology approach.

Imane El Meouche
IAME, UMR 1137 INSERM - Université de Paris, Faculté de Médecine Université de Paris, http://www.iame-research.center/
Dr. Imane El Meouche completed her PhD in microbiology at the University of Rouen studying autolysis and toxins expression in Clostridium difficile. She next moved to the US and did her post-doc in the Dunlop lab. She focused on the emergence of transient and permanent antibiotic resistance in Escherichia coli. Now, as an INSERM researcher, she is working to understand the mechanisms of antibiotic resistance and tolerance in E. coli using in vitro and in vivo approaches.
Jacques Monod stated that the study of bacterial cell growth is the basic microbiology method (Monod 1949). Each phase of growth defined more than 70 years is of new interest in the light of our current knowledge. Notably, there is an increasing focus on bacterial physiology and the interplay with the environment, especially in infections treatment failures. For example, (i) the duration of the lag time before resuming growth can be heterogeneous between isogenic cells and lead to various responses to antibiotics. Understanding the origin of this heterogeneity and its mechanistic basis is critical to fighting bacterial infections. (ii) The exponential growth phase offers a unique means to reach a meta-stable steady-state in batch cultures that allows for the generation of reproducible physiological states. This physiological steady state also informs us about the fundamental trade-offs in resources allocation at the cellular level that rule bacterial cell proliferation. (iii) Mechanisms controlling entry into and exit from the stationary phase are also of paramount importance, as they encompass the basics of stress resistance until the extreme phenotype of dormancy is observed in clinical contexts and natural environments.
As the field of bacterial cell biology has evolved with recent technological advances, we believe it is time to revisit classical protocols and state-of-the-art methods to explore bacterial proliferation under conditions ever closer to natural habitats and wild microbes. The tools presented in these protocols yield quantitative measurements through the impulse of standard mathematical and statistical procedures, computational models, and artificial intelligence.
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2023
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