Identification of a phage-derived depolymerase specific for KL64 capsule of Klebsiella pneumoniae and its anti-biofilm effect

The increasing prevalence of Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a serious threat to global health. Phages and phage-derived enzymes gained increasing attention for controling CRKP infections. In this study, a lytic phage P510 infecting KL64 type K. pneumoniae was isolated and ch...

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Published in:Virus genes Vol. 57; no. 5; pp. 434 - 442
Main Authors: Li, Min, Li, Pei, Chen, Long, Guo, Genglin, Xiao, Yuyi, Chen, Liang, Du, Hong, Zhang, Wei
Format: Journal Article
Language:English
Published: New York Springer US 01.10.2021
Springer Nature B.V
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ISSN:0920-8569, 1572-994X, 1572-994X
Online Access:Get full text
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Summary:The increasing prevalence of Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a serious threat to global health. Phages and phage-derived enzymes gained increasing attention for controling CRKP infections. In this study, a lytic phage P510 infecting KL64 type K. pneumoniae was isolated and characterized. Whole genome analysis and electron microscopy analysis showed that phage P510 belonged to genus Przondovirus , family Autographiviridae , the order Caudovirales . The tail fiber protein of the phage was predicted to encode capsule depolymerase. Further analysis demonstrated that recombinant depolymerase P510dep had polysaccharide-degrading activity against KL64-types capsule of K. pneumoniae , and its lysis spectrum matched to host range of phage P510. We also demonstrated that the recombinant depolymerase was able to significantly inhibit biofilm formation. The discovery of the phage-derived depolymerase lays the foundation for controlling the spread of CRKPs.
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ISSN:0920-8569
1572-994X
1572-994X
DOI:10.1007/s11262-021-01847-8