4.8 Article

Spatial patterns in phage-Rhizobium coevolutionary interactions across regions of common bean domestication

Journal

ISME JOURNAL
Volume 15, Issue 7, Pages 2092-2106

Publisher

SPRINGERNATURE
DOI: 10.1038/s41396-021-00907-z

Keywords

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Funding

  1. PAPIIT-UNAM [IN209817]
  2. CCG-UNAM
  3. DGAPA-UNAM
  4. NSF [DEB-1457508, IOS-1759048]

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Through the study of four phage-Rhizobium communities in Mexico and Argentina, it was found that both phage and host diversity are spatially structured. Results showed that phage local adaptation and host maladaptation play key roles in shaping phage-host interactions. The study also revealed a nested network of interactions between phages and hosts, with their genetic identity and geographic origin influencing the interactions.
Bacteriophages play significant roles in the composition, diversity, and evolution of bacterial communities. Despite their importance, it remains unclear how phage diversity and phage-host interactions are spatially structured. Local adaptation may play a key role. Nitrogen-fixing symbiotic bacteria, known as rhizobia, have been shown to locally adapt to domesticated common bean at its Mesoamerican and Andean sites of origin. This may affect phage-rhizobium interactions. However, knowledge about the diversity and coevolution of phages with their respective Rhizobium populations is lacking. Here, through the study of four phage-Rhizobium communities in Mexico and Argentina, we show that both phage and host diversity is spatially structured. Cross-infection experiments demonstrated that phage infection rates were higher overall in sympatric rhizobia than in allopatric rhizobia except for one Argentinean community, indicating phage local adaptation and host maladaptation. Phage-host interactions were shaped by the genetic identity and geographic origin of both the phage and the host. The phages ranged from specialists to generalists, revealing a nested network of interactions. Our results suggest a key role of local adaptation to resident host bacterial communities in shaping the phage genetic and phenotypic composition, following a similar spatial pattern of diversity and coevolution to that in the host.

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