Abstract

Correct chromosomal segregation, coordinated with cell division, is crucial for bacterial survival, but despite extensive studies, the mechanisms underlying this remain incompletely understood in mycobacteria. We report a detailed investigation of the dynamic interactions between ParA and ParB partitioning proteins in Mycobacterium smegmatis using microfluidics and time-lapse fluorescence microscopy to observe both proteins simultaneously. During growth and division, ParB presents as a focused fluorescent spot that subsequently splits in two. One focus moves towards a higher concentration of ParA at the new pole, while the other moves towards the old pole. We show ParB movement is in part an active process that does not rely on passive movement associated with cell growth. In some cells, another round of ParB segregation starts before cell division is complete, consistent with initiation of a second round of chromosome replication. ParA fluorescence distribution correlates with cell size, and in sister cells, the larger cell inherits a local peak of concentrated ParA, while the smaller sister inherits more homogeneously distributed protein. Cells which inherit more ParA grow faster than their sister cell, raising the question of whether inheritance of a local concentration of ParA provides a growth advantage. Alterations in levels of ParA and ParB were also found to disturb cell growth.

Highlights

  • The ParABS system was originally described in the segregation of low-copy number plasmids, but homologous proteins have been identified in many bacteria, including the genus Mycobacterium [1,2,3,4,5,6,7,8], where they participate in chromosome partitioning [9]

  • Understanding how chromosomes are segregated in mycobacteria is of critical importance, with the increase in Mycobacterium tuberculosis drug-resistant strains requiring the urgent development of novel therapeutics [10]

  • We report here a detailed analysis of the movement of both ParA and ParB during the growth and division of M. smegmatis using time-lapse microscopy and microfluidics, and propose a model of their dynamics (Fig 7)

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Summary

Introduction

The ParABS system was originally described in the segregation of low-copy number plasmids, but homologous proteins have been identified in many bacteria, including the genus Mycobacterium [1,2,3,4,5,6,7,8], where they participate in chromosome partitioning [9]. Understanding how chromosomes are segregated in mycobacteria is of critical importance, with the increase in Mycobacterium tuberculosis drug-resistant strains requiring the urgent development of novel therapeutics [10]. Novel features of ParAB dynamics in mycobacteria. The ONIX microfluidics platform was provided by an Imperial College Trust Collaborative Research Award (https://www.imperial.ac.uk/admin-services/ secretariat/secretariat/what-we-do/imperialcollege-trust/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

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