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1.
Elife ; 72018 12 18.
Article in English | MEDLINE | ID: mdl-30558711

ABSTRACT

A single cheating mutant can lead to the invasion and eventual eradication of cooperation from a population. Consequently, cheat invasion is often considered equal to extinction in empirical and theoretical studies of cooperator-cheat dynamics. But does cheat invasion necessarily equate extinction in nature? By following the social dynamics of iron metabolism in Pseudomonas aeruginosa during cystic fibrosis lung infection, we observed that individuals evolved to replace cooperation with a 'private' behaviour. Phenotypic assays showed that cooperative iron acquisition frequently was upregulated early in infection, which, however, increased the risk of cheat invasion. With whole-genome sequencing we showed that if, and only if, cooperative iron acquisition is lost from the population, a private system was upregulated. The benefit of upregulation depended on iron availability. These findings highlight the importance of social dynamics of natural populations and emphasizes the potential impact of past social interaction on the evolution of private traits.


Subject(s)
Gene Expression Regulation, Bacterial , Iron/metabolism , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/metabolism , Cystic Fibrosis/complications , Genetics, Population , Pseudomonas aeruginosa/genetics , Whole Genome Sequencing
2.
Biotechniques ; 59(3): 163-6, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26345510

ABSTRACT

Current gene synthesis methods often incorporate a PCR amplification step in order to yield final material sufficient for resolution from multiple off-products. These amplification steps can cause stochastic sampling effects that propagate errors in gene synthesis or decrease variability when applied to the construction of randomized libraries. We have developed a simple DNA polymerase-based gene synthesis reaction, polymerase step reaction (PSR), that assembles DNA oligonucleotides in a unidirectional fashion without the need for amplification. We demonstrate that PSR is efficient, with little off-product production, no detectable error propagation, and maximized variability in the synthesis of a phage display library.


Subject(s)
DNA-Directed DNA Polymerase/metabolism , Gene Library , DNA/genetics , DNA/isolation & purification , DNA Primers , DNA, Single-Stranded/genetics , DNA, Single-Stranded/isolation & purification , DNA-Directed DNA Polymerase/genetics , Nucleic Acid Amplification Techniques/methods , Polymerase Chain Reaction , Single-Domain Antibodies/genetics
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