共 8 条
Characterization of vB_Kpn_F48, a Newly Discovered Lytic Bacteriophage for Klebsiella pneumoniae of Sequence Type 101
被引:36
|作者:
Ciacci, Nagaia
[1
,2
]
D'Andrea, Marco Maria
[1
,2
]
Marmo, Pasquale
[1
]
Dematte, Elisa
[3
]
Amisano, Francesco
[4
]
Di Pilato, Vincenzo
[5
]
Fraziano, Maurizio
[1
]
Lupetti, Pietro
[6
]
Rossolini, Gian Maria
[5
,7
]
Thaller, Maria Cristina
[1
]
机构:
[1] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[2] Univ Siena, Dept Med Biotechnol, I-53100 Siena, Italy
[3] Univ Trento, Ctr Integrat Biol, CIBIO, I-38122 Trento, Italy
[4] Univ Liege, InBioS Ctr Prot Engn, Dept Life Sci, B-4000 Liege, Belgium
[5] Univ Florence, Dept Expt & Clin Med, I-50134 Florence, Italy
[6] Univ Siena, Dept Life Sci, I-53100 Siena, Italy
[7] Florence Careggi Univ Hosp, Clin Microbiol & Virol Unit, I-50134 Florence, Italy
来源:
VIRUSES-BASEL
|
2018年
/
10卷
/
09期
关键词:
bacteriophage;
Tevenvirinae;
Klebsiella pneumoniae carbapenemase (KPC);
K;
pneumoniae;
sequence type 101;
Klebsiella pneumoniae ST101;
TRANSFER-RNA GENES;
ESCHERICHIA-COLI;
MOLECULAR EPIDEMIOLOGY;
ANTIBIOTIC-RESISTANCE;
HOST-RANGE;
OUTBREAK;
CLONE;
PHAGES;
AGENT;
ST101;
D O I:
10.3390/v10090482
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
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.
引用
收藏
页数:16
相关论文