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Reprioritization of biofilm metabolism is associated with nutrient adaptation and long-term survival of Haemophilus influenzae.


ABSTRACT: Nontypeable Haemophilus influenzae (NTHI) is a human-restricted pathogen with an essential requirement for heme-iron acquisition. We previously demonstrated that microevolution of NTHI promotes stationary phase survival in response to transient heme-iron restriction. In this study, we examine the metabolic contributions to biofilm formation using this evolved NTHI strain, RM33. Quantitative analyses identified 29 proteins, 55 transcripts, and 31 metabolites that significantly changed within in vitro biofilms formed by RM33. The synthesis of all enzymes within the tryptophan and glycogen pathways was significantly increased in biofilms formed by RM33 compared with the parental strain. In addition, increases were observed in metabolite transport, adhesin production, and DNA metabolism. Furthermore, we observed pyruvate as a pivotal point in the metabolic pathways associated with changes in cAMP phosphodiesterase activity during biofilm formation. Taken together, changes in central metabolism combined with increased stores of nutrients may serve to counterbalance nutrient sequestration.

SUBMITTER: Harrison A 

PROVIDER: S-EPMC6831627 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Reprioritization of biofilm metabolism is associated with nutrient adaptation and long-term survival of <i>Haemophilus influenzae</i>.

Harrison Alistair A   Hardison Rachael L RL   Wallace Rachel M RM   Fitch James J   Heimlich Derek R DR   Bryan Meghan O' MO   Dubois Laura L   John-Williams Lisa St LS   Sebra Robert P RP   White Peter P   Moseley M Arthur MA   Thompson J Will JW   Justice Sheryl S SS   Mason Kevin M KM  

NPJ biofilms and microbiomes 20191105 1


Nontypeable <i>Haemophilus influenzae</i> (NTHI) is a human-restricted pathogen with an essential requirement for heme-iron acquisition. We previously demonstrated that microevolution of NTHI promotes stationary phase survival in response to transient heme-iron restriction. In this study, we examine the metabolic contributions to biofilm formation using this evolved NTHI strain, RM33. Quantitative analyses identified 29 proteins, 55 transcripts, and 31 metabolites that significantly changed with  ...[more]

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