Literature DB >> 24013213

Co-evolutionary dynamics of the bacteria Vibrio sp. CV1 and phages V1G, V1P1, and V1P2: implications for phage therapy.

Camilo Barbosa1, Patrick Venail, Angela V Holguin, Martha J Vives.   

Abstract

Bacterial infections are the second largest cause of mortality in shrimp hatcheries. Among them, bacteria from the genus Vibrio constitute a major threat. As the use of antibiotics may be ineffective and banned from the food sector, alternatives are required. Historically, phage therapy, which is the use of bacteriophages, is thought to be a promising option to fight against bacterial infections. However, as for antibiotics, resistance can be rapidly developed. Since the emergence of resistance is highly undesirable, a formal characterization of the dynamics of its acquisition is mandatory. Here, we explored the co-evolutionary dynamics of resistance between the bacteria Vibrio sp. CV1 and the phages V1G, V1P1, and V1P2. Single-phage treatments as well as a cocktail composed of the three phages were considered. We found that in the presence of a single phage, bacteria rapidly evolved resistance, and the phages decreased their infectivity, suggesting that monotherapy may be an inefficient treatment to fight against Vibrio infections in shrimp hatcheries. On the contrary, the use of a phage cocktail considerably delayed the evolution of resistance and sustained phage infectivity for periods in which shrimp larvae are most susceptible to bacterial infections, suggesting the simultaneous use of multiple phages as a serious strategy for the control of vibriosis. These findings are very promising in terms of their consequences to different industrial and medical scenarios where bacterial infections are present.

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Year:  2013        PMID: 24013213     DOI: 10.1007/s00248-013-0284-2

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  37 in total

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3.  The costs of evolving resistance in heterogeneous parasite environments.

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Review 4.  Bacteriophage resistance mechanisms.

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7.  The evolution of specificity in evolving and coevolving antagonistic interactions between a bacteria and its phage.

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Journal:  Front Microbiol       Date:  2016-03-15       Impact factor: 5.640

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7.  Phage Reduce Stability for Regaining Infectivity during Antagonistic Coevolution with Host Bacterium.

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9.  Parasite diversity drives rapid host dynamics and evolution of resistance in a bacteria-phage system.

Authors:  Alex Betts; Danna R Gifford; R Craig MacLean; Kayla C King
Journal:  Evolution       Date:  2016-04-19       Impact factor: 3.694

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Journal:  PLoS Biol       Date:  2018-10-03       Impact factor: 8.029

  10 in total

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