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Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model

Bacteriophages (phages) or viruses that specifically infect bacteria have widely been studied as biocontrol agents against animal and plant bacterial diseases. They offer many advantages compared to antibiotics. The American Foulbrood (AFB) is a bacterial disease affecting honeybee larvae caused by...

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Autores principales: Ribeiro, Henrique G., Correia, Rossana, Moreira, Tiago, Vilas Boas, Diana, Azeredo, Joana, Oliveira, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345884/
https://www.ncbi.nlm.nih.gov/pubmed/30679452
http://dx.doi.org/10.1038/s41598-018-36432-x
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author Ribeiro, Henrique G.
Correia, Rossana
Moreira, Tiago
Vilas Boas, Diana
Azeredo, Joana
Oliveira, Ana
author_facet Ribeiro, Henrique G.
Correia, Rossana
Moreira, Tiago
Vilas Boas, Diana
Azeredo, Joana
Oliveira, Ana
author_sort Ribeiro, Henrique G.
collection PubMed
description Bacteriophages (phages) or viruses that specifically infect bacteria have widely been studied as biocontrol agents against animal and plant bacterial diseases. They offer many advantages compared to antibiotics. The American Foulbrood (AFB) is a bacterial disease affecting honeybee larvae caused by Paenibacillus larvae. Phages can be very significant in fighting it mostly due to European restrictions to the use of antibiotics in beekeeping. New phages able to control P. larvae in hives have already been reported with satisfactory results. However, the efficacy and feasibility of administering phages indirectly to larvae through their adult workers only by providing phages in bees’ feeders has never been evaluated. This strategy is considered herein the most feasible as far as hive management is concerned. This in vivo study investigated the ability of a phage to reach larvae in an infective state after oral administration to honeybees. The screening (by direct PFU count) and quantification (by quantitative PCR) of the phage in bee organs and in larvae after ingestion allowed us to conclude that despite 10(4) phages reaching larvae only an average of 32 were available to control the spread of the disease. The fast inactivation of many phages in royal jelly could compromise this therapeutic approach. The protection of phages from hive-derived conditions should be thus considered in further developments for AFB treatment.
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spelling pubmed-63458842019-01-29 Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model Ribeiro, Henrique G. Correia, Rossana Moreira, Tiago Vilas Boas, Diana Azeredo, Joana Oliveira, Ana Sci Rep Article Bacteriophages (phages) or viruses that specifically infect bacteria have widely been studied as biocontrol agents against animal and plant bacterial diseases. They offer many advantages compared to antibiotics. The American Foulbrood (AFB) is a bacterial disease affecting honeybee larvae caused by Paenibacillus larvae. Phages can be very significant in fighting it mostly due to European restrictions to the use of antibiotics in beekeeping. New phages able to control P. larvae in hives have already been reported with satisfactory results. However, the efficacy and feasibility of administering phages indirectly to larvae through their adult workers only by providing phages in bees’ feeders has never been evaluated. This strategy is considered herein the most feasible as far as hive management is concerned. This in vivo study investigated the ability of a phage to reach larvae in an infective state after oral administration to honeybees. The screening (by direct PFU count) and quantification (by quantitative PCR) of the phage in bee organs and in larvae after ingestion allowed us to conclude that despite 10(4) phages reaching larvae only an average of 32 were available to control the spread of the disease. The fast inactivation of many phages in royal jelly could compromise this therapeutic approach. The protection of phages from hive-derived conditions should be thus considered in further developments for AFB treatment. Nature Publishing Group UK 2019-01-24 /pmc/articles/PMC6345884/ /pubmed/30679452 http://dx.doi.org/10.1038/s41598-018-36432-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ribeiro, Henrique G.
Correia, Rossana
Moreira, Tiago
Vilas Boas, Diana
Azeredo, Joana
Oliveira, Ana
Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title_full Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title_fullStr Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title_full_unstemmed Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title_short Bacteriophage biodistribution and infectivity from honeybee to bee larvae using a T7 phage model
title_sort bacteriophage biodistribution and infectivity from honeybee to bee larvae using a t7 phage model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345884/
https://www.ncbi.nlm.nih.gov/pubmed/30679452
http://dx.doi.org/10.1038/s41598-018-36432-x
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