Genetic determinants of host tropism in Klebsiella phages

被引:39
作者
Beamud, Beatriz [1 ,2 ]
Garcia-Gonzalez, Neris [1 ,2 ]
Gomez-Ortega, Mar [1 ]
Gonzalez-Candelas, Fernando [1 ,2 ]
Domingo-Calap, Pilar [2 ]
Sanjuan, Rafael [2 ]
机构
[1] Univ Valencia, Joint Res Unit Infect & Publ Hlth, FISABIO, Valencia 46020, Spain
[2] Univ Valencia, Inst Integrat Syst Biol I2SysBio, CSIC, Paterna 46980, Spain
关键词
PHAGE; PROTEIN; TAIL; DIVERSITY; INFECTION; RANGE; BACTERIOPHAGES; POLYSACCHARIDE; DEPOLYMERASE; PNEUMONIAE;
D O I
10.1016/j.celrep.2023.112048
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bacteriophages play key roles in bacterial ecology and evolution and are potential antimicrobials. However, the determinants of phage-host specificity remain elusive. Here, we isolate 46 phages to challenge 138 repre-sentative clinical isolates of Klebsiella pneumoniae, a widespread opportunistic pathogen. Spot tests show a narrow host range for most phages, with < 2% of 6,319 phage-host combinations tested yielding detectable interactions. Bacterial capsule diversity is the main factor restricting phage host range. Consequently, phage-encoded depolymerases are key determinants of host tropism, and depolymerase sequence types are associated with the ability to infect specific capsular types across phage families. However, all phages with a broader host range found do not encode canonical depolymerases, suggesting alternative modes of entry. These findings expand our knowledge of the complex interactions between bacteria and their vi-ruses and point out the feasibility of predicting the first steps of phage infection using bacterial and phage genome sequences.
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页数:21
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