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Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101

Resistance to carbapenems in Enterobacteriaceae, including Klebsiella pneumoniae, represents a major clinical problem given the lack of effective alternative antibiotics. Bacteriophages could provide a valuable tool to control the dissemination of antibiotic resistant isolates, for the decolonizatio...

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Autores principales: Ciacci, Nagaia, D’Andrea, Marco Maria, Marmo, Pasquale, Demattè, Elisa, Amisano, Francesco, Di Pilato, Vincenzo, Fraziano, Maurizio, Lupetti, Pietro, Rossolini, Gian Maria, Thaller, Maria Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163469/
https://www.ncbi.nlm.nih.gov/pubmed/30205588
http://dx.doi.org/10.3390/v10090482
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author Ciacci, Nagaia
D’Andrea, Marco Maria
Marmo, Pasquale
Demattè, Elisa
Amisano, Francesco
Di Pilato, Vincenzo
Fraziano, Maurizio
Lupetti, Pietro
Rossolini, Gian Maria
Thaller, Maria Cristina
author_facet Ciacci, Nagaia
D’Andrea, Marco Maria
Marmo, Pasquale
Demattè, Elisa
Amisano, Francesco
Di Pilato, Vincenzo
Fraziano, Maurizio
Lupetti, Pietro
Rossolini, Gian Maria
Thaller, Maria Cristina
author_sort Ciacci, Nagaia
collection PubMed
description Resistance to carbapenems in Enterobacteriaceae, including Klebsiella pneumoniae, represents a major clinical problem given the lack of effective alternative antibiotics. Bacteriophages could provide a valuable tool to control the dissemination of antibiotic resistant isolates, for the decolonization of colonized individuals and for treatment purposes. In this work, we have characterized a lytic bacteriophage, named vB_Kpn_F48, specific for K. pneumoniae isolates belonging to clonal group 101. Phage vB_Kpn_F48 was classified as a member of Myoviridae, order Caudovirales, on the basis of transmission electron microscopy analysis. Physiological characterization demonstrated that vB_Kpn_F48 showed a narrow host range, a short latent period, a low burst size and it is highly stable to both temperature and pH variations. High throughput sequencing and bioinformatics analysis revealed that the phage is characterized by a 171 Kb dsDNA genome that lacks genes undesirable for a therapeutic perspective such integrases, antibiotic resistance genes and toxin encoding genes. Phylogenetic analysis suggests that vB_Kpn_F48 is a T4-like bacteriophage which belongs to a novel genus within the Tevenvirinae subfamily, which we tentatively named “F48virus”. Considering the narrow host range, the genomic features and overall physiological parameters phage vB_Kpn_F48 could be a promising candidate to be used alone or in cocktails for phage therapy applications.
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spelling pubmed-61634692018-10-11 Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101 Ciacci, Nagaia D’Andrea, Marco Maria Marmo, Pasquale Demattè, Elisa Amisano, Francesco Di Pilato, Vincenzo Fraziano, Maurizio Lupetti, Pietro Rossolini, Gian Maria Thaller, Maria Cristina Viruses Article Resistance to carbapenems in Enterobacteriaceae, including Klebsiella pneumoniae, represents a major clinical problem given the lack of effective alternative antibiotics. Bacteriophages could provide a valuable tool to control the dissemination of antibiotic resistant isolates, for the decolonization of colonized individuals and for treatment purposes. In this work, we have characterized a lytic bacteriophage, named vB_Kpn_F48, specific for K. pneumoniae isolates belonging to clonal group 101. Phage vB_Kpn_F48 was classified as a member of Myoviridae, order Caudovirales, on the basis of transmission electron microscopy analysis. Physiological characterization demonstrated that vB_Kpn_F48 showed a narrow host range, a short latent period, a low burst size and it is highly stable to both temperature and pH variations. High throughput sequencing and bioinformatics analysis revealed that the phage is characterized by a 171 Kb dsDNA genome that lacks genes undesirable for a therapeutic perspective such integrases, antibiotic resistance genes and toxin encoding genes. Phylogenetic analysis suggests that vB_Kpn_F48 is a T4-like bacteriophage which belongs to a novel genus within the Tevenvirinae subfamily, which we tentatively named “F48virus”. Considering the narrow host range, the genomic features and overall physiological parameters phage vB_Kpn_F48 could be a promising candidate to be used alone or in cocktails for phage therapy applications. MDPI 2018-09-09 /pmc/articles/PMC6163469/ /pubmed/30205588 http://dx.doi.org/10.3390/v10090482 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ciacci, Nagaia
D’Andrea, Marco Maria
Marmo, Pasquale
Demattè, Elisa
Amisano, Francesco
Di Pilato, Vincenzo
Fraziano, Maurizio
Lupetti, Pietro
Rossolini, Gian Maria
Thaller, Maria Cristina
Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title_full Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title_fullStr Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title_full_unstemmed Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title_short Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
title_sort characterization of vb_kpn_f48, a newly discovered lytic bacteriophage for klebsiella pneumoniae of sequence type 101
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163469/
https://www.ncbi.nlm.nih.gov/pubmed/30205588
http://dx.doi.org/10.3390/v10090482
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