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Brynildsen, M. P.

Publications and source records attributed to Brynildsen, M. P..

2 recordsLinked to original sources

Gre factors protect against phenotypic diversification and cheating in Escherichia coli populations under toxic metabolite stress

Nitric oxide ({middle dot}NO) is one of the toxic metabolites that bacteria can be exposed to within phagosomes. Gre factors, which are also known as transcript cleavage factors or transcription elongation factors, relieve back-tracked transcription elongation complexes by cleaving nascent RNAs, which allows transcription to resume after stalling. Here we discovered that loss of both Gre factors in E. coli, GreA and GreB, significantly compromised {middle dot}NO detoxification through a phenotypic diversification of the population. Under normal culturing conditions, both wild-type and {Delta}greA{Delta}greB synthesized protein uniformly. However, treatment with {middle dot}NO led to bimodal protein expression in {Delta}greA{Delta}greB, whereas wild-type remained unimodal. Interestingly, exposure to another toxic metabolite of phagosomes, hydrogen peroxide (H2O2), produced similar results. We found that the diversification in {Delta}greA{Delta}greB cultures required E. coli RNAP, occurred at the level of transcription, and could produce cheating where transcriptionally-deficient cells benefit from the detoxification activities of the transcriptionally-proficient subpopulation. Collectively, these results indicate that Gre factors bolster bacterial defenses by preventing phenotypic diversification and cheating in environments with fast-diffusing toxic metabolites. ImportanceToxic metabolite stress occurs in a broad range of contexts that are important to human health, microbial ecology, and biotechnology; whereas Gre factors are highly conserved throughout the bacterial kingdom. Here we discovered that the Gre factors of E. coli prevent phenotypic diversification under toxic metabolite stress. Such conformist regulation improves populationwide removal of those stressors and protects against cheating, where one subpopulation commits resources to counter a threat, and the other subpopulation does not, yet both subpopulations benefit.

microbiology↗

Genome-wide mapping of fluoroquinolone-stabilized DNA gyrase cleavage sites displays drug specific effects that correlate with bacterial persistence

Persisters are rare phenotypic variants that are suspected to be culprits of recurrent infections. Fluoroquinolones (FQs) are a class of antibiotic that facilitate DNA damage by stabilizing type II topoisomerases when they are in a complex with cleaved DNA. In Escherichia coli, DNA gyrase is the primary FQ target, and previous work has demonstrated that persisters are not spared from FQ-induced DNA damage. Since DNA gyrase cleavage sites (GCSs) largely govern the sites of DNA damage from FQ treatment, we hypothesized that GCS characteristics (e.g., number, strength, location) may influence persistence. To test this hypothesis, we measured genome-wide GCS distributions after treatment with a panel of FQs. We found drug-specific effects on the GCS distribution and discovered a strong negative correlation between the cumulative cleavage strength across the chromosome and FQ persister levels. Further experiments and analyses suggested that persistence was not governed by cleavage to individual sites, but rather survival was a function of the cumulative GCS distribution. Together, these findings demonstrate FQ-specific differences in GCS distribution that correlate with persister levels and suggest that FQs that better stabilize DNA gyrase in cleaved complexes with DNA will lead to lower levels of persistence.

microbiology↗