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Complex bacterial environments can be composed indeed of several underrepresented species, difficult to isolate.
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Interactions between different bacterial communities and their environments can be comprehensively analyzed by metagenomics research.
First, bacterial groups in different environments can be compared in terms of CRISPR dynamics to assess the relative importance of CRISPR in these environments.
Bacterial persistence in food processing environments can be due to the existence of harborage sites that are colonized by bacteria and cannot be effectively cleaned or disinfected or can be due to the enhanced ability of some particular strains to grow or survive and therefore persist in industrial settings [ 27].
Bacterial flora in fish and water environment can be different in various geographical areas.
These results suggest that polarity of the solvent environment can be manipulated as a design parameter to control or modify the bacterial adhesion process.
The environment can be unforgiving.
A laboratory environment can be treacherous.
We would not venture to argue that the conditions we use are the 'correct' ones: rather, we present our results as examples of how improved lab models of specific infection contexts can be developed and used, and to demonstrate how different the fitness effects of a bacterial phenotype can be in different environments.
In line with these results, metagenomic analysis showed that MUC and PEC benthic microbial communities share the main common bacterial phyla found in coastal environments, although can be distinguish by greater abundance of Cyanobacteria in MUC and Deltaproteobacteria in PEC.
But bacterial sequences can be recognized and discarded, he said.
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