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Erosion of functional independence early in the evolution of a microbial mutualism.


ABSTRACT: Many species have evolved to function as specialized mutualists, often to the detriment of their ability to survive independently. However, there are few, if any, well-controlled observations of the evolutionary processes underlying the genesis of new mutualisms. Here, we show that within the first 1,000 generations of initiating independent syntrophic interactions between a sulfate reducer (Desulfovibrio vulgaris) and a hydrogenotrophic methanogen (Methanococcus maripaludis), D. vulgaris frequently lost the capacity to grow by sulfate respiration, thus losing the primary physiological attribute of the genus. The loss of sulfate respiration was a consequence of mutations in one or more of three key genes in the pathway for sulfate respiration, required for sulfate activation (sat) and sulfate reduction to sulfite (apsA or apsB). Because loss-of-function mutations arose rapidly and independently in replicated experiments, and because these mutations were correlated with enhanced growth rate and productivity, gene loss could be attributed to natural selection, even though these mutations should significantly restrict the independence of the evolved D. vulgaris. Together, these data present an empirical demonstration that specialization for a mutualistic interaction can evolve by natural selection shortly after its origin. They also demonstrate that a sulfate-reducing bacterium can readily evolve to become a specialized syntroph, a situation that may have often occurred in nature.

SUBMITTER: Hillesland KL 

PROVIDER: S-EPMC4205623 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

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Erosion of functional independence early in the evolution of a microbial mutualism.

Hillesland Kristina L KL   Lim Sujung S   Flowers Jason J JJ   Turkarslan Serdar S   Pinel Nicolas N   Zane Grant M GM   Elliott Nicholas N   Qin Yujia Y   Wu Liyou L   Baliga Nitin S NS   Zhou Jizhong J   Wall Judy D JD   Stahl David A DA  

Proceedings of the National Academy of Sciences of the United States of America 20140929 41


Many species have evolved to function as specialized mutualists, often to the detriment of their ability to survive independently. However, there are few, if any, well-controlled observations of the evolutionary processes underlying the genesis of new mutualisms. Here, we show that within the first 1,000 generations of initiating independent syntrophic interactions between a sulfate reducer (Desulfovibrio vulgaris) and a hydrogenotrophic methanogen (Methanococcus maripaludis), D. vulgaris freque  ...[more]

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