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Biology subjects

Ticak, T.

Publications and source records attributed to Ticak, T..

2 recordsLinked to original sources

Antibiotic persistence does not cause phenotypic heterogeneity in tolerance of Escherichia coli to formaldehyde stress but can preserve it through time

The phenomenon of phenotypic heterogeneity, where an isogenic population expresses varying phenotypes, has been uncovered for an expanding variety of organisms and traits. This heterogeneity in phenotype can be physiologically relevant, such as the ability for antibiotic persistence to allow populations to survive lethal conditions due to rare cells being in a slow or non-growing state. Recently, it was discovered that Methylorubrum extorquens, a facultative methylotroph, possesses a continuous spectrum of phenotypic states conferring tolerance to formaldehyde. Formaldehyde is a toxin produced by M. extorquens during growth on methanol. The phenotypic tolerance allowed rapid growth on levels of formaldehyde which were lethal to the majority of the population. Transcriptomics indicated this may be due to upregulation of proteins that attenuate oxidative stress and protein damage rather than increasing formaldehyde oxidation to prevent accumulation. These data suggested that heterogeneity to formaldehyde stress may be present even in non-methylotrophic organisms that do not routinely produce large quantities of formaldehyde, and thus widely distributed across bacteria. To investigate this, we tested Escherichia coli for heterogeneity to formaldehyde stress during growth on glucose. Like M. extorquens, E. coli populations have a wide, continuous range of formaldehyde tolerance thresholds and this tolerance was reversible. Several other features, however, were different from what was found for M. extorquens. Most E. coli growth occurred after formaldehyde levels had dropped, suggesting that persistence could be the cause. The dynamics of antibiotic persistence and formaldehyde tolerance were both tracked but found to not be correlated. On the other hand, the persister cell state can maintain formaldehyde tolerance. These data suggest that persistence can preserve phenotypic heterogeneities in other traits, further expanding its potential role in helping cells survive environmental stressors.

microbiology↗

EfgA is a conserved formaldehyde sensor that halts bacterial translation in response to elevated formaldehyde

Normal cellular processes give rise to toxic metabolites that cells must mitigate. Formaldehyde is a universal stressor and potent metabolic toxin that is generated in organisms from bacteria to humans. Methylotrophic bacteria such as Methylorubrum extorquens face an acute challenge due to their production of formaldehyde as an obligate central intermediate of single-carbon metabolism. Mechanisms to sense and respond to formaldehyde were speculated to exist in methylotrophs for decades but had never been discovered. Here we identify a member of the DUF336 domain family, named efgA for enhanced formaldehyde growth, that plays an important role in endogenous formaldehyde stress response in M. extorquens PA1 and is found almost exclusively in methylotrophic taxa. Our experimental analyses reveal that EfgA is a formaldehyde sensor that inhibits translation in response to elevated levels of formaldehyde. Heterologous expression of EfgA in Escherichia coli increases formaldehyde resistance, indicating that its interaction partners are widespread and conserved and may include translational machinery. EfgA represents the first example of a formaldehyde stress response system that does not involve enzymatic detoxification. Thus, EfgA comprises a unique stress response mechanism in bacteria, whereby a single protein directly senses elevated levels of a toxic intracellular metabolite and modulates translational activity.

microbiology↗