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.
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页数:16
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