Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae

Carbapenem-resistant Klebsiella pneumoniae (CRKP) pose a significant threat to global public health. In present research, a total of 80 CRKP strains belonging to ST11 were collected with 70% (56 of 80 isolates) expressing a K47 capsular type. Thus, it is significant to prevent and control infections...

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Main Authors: Yannan Liu, Sharon Shui Yee Leung, Yong Huang, Yatao Guo, Ning Jiang, Puyuan Li, Jichao Chen, Rentao Wang, Changqing Bai, Zhiqiang Mi, Zhancheng Gao
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2020.00218/full
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spelling doaj-bba2870669e0473694c2b294f027d9d12020-11-25T03:14:55ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-02-011110.3389/fmicb.2020.00218505713Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniaeYannan Liu0Sharon Shui Yee Leung1Yong Huang2Yatao Guo3Ning Jiang4Puyuan Li5Jichao Chen6Rentao Wang7Changqing Bai8Zhiqiang Mi9Zhancheng Gao10Department of Respiratory and Critical Care Medicine, Peking University People’s Hospital, Beijing, ChinaSchool of Pharmacy, The Chinese University of Hong Kong, Shatin, Hong KongState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, Peking University People’s Hospital, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, Peking University People’s Hospital, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, The Fifth Medical Centre of Chinese PLA General Hospital, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, Aerospace Center Hospital, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, The First Medical Centre of Chinese PLA General Hospital, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, The Fifth Medical Centre of Chinese PLA General Hospital, Beijing, ChinaState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, ChinaDepartment of Respiratory and Critical Care Medicine, Peking University People’s Hospital, Beijing, ChinaCarbapenem-resistant Klebsiella pneumoniae (CRKP) pose a significant threat to global public health. In present research, a total of 80 CRKP strains belonging to ST11 were collected with 70% (56 of 80 isolates) expressing a K47 capsular type. Thus, it is significant to prevent and control infections caused by these bacteria. Capsule depolymerases could degrade bacterial surface polysaccharides to reduce their virulence and expose bacteria to host immune attack. Previous studies have demonstrated the potential of phage-encoded depolymerases as antivirulent agents in treating CRKP infections in vitro and in vivo. Here, two capsule depolymerases (Dpo42 and Dpo43) derived from phage IME205 were expressed and characterized. Although both depolymerases act on strains with a capsular serotype K47, they are active against different subsets of strains, indicating subtle differences in capsule composition that exist within this serotype. The host range of phage IME205 matched to the sum of specificity range of Dpo42 and Dpo43. These two enzymes maintained stable activity in a relatively broad range of pH levels (pH 5.0–8.0 for Dpo42 and pH 4.0–8.0 for Dpo43) and temperatures (20–70°C). Besides, both Dpo42 and Dpo43 could make host bacteria fully susceptible to the killing effect of serum complement and display no hemolytic activity to erythrocytes. In summary, capsule depolymerases are promising antivirulent agents to combat CRKP infections.https://www.frontiersin.org/article/10.3389/fmicb.2020.00218/fullKlebsiella pneumoniaecarbapenem resistancecapsular typecapsule depolymeraseantivirulence
collection DOAJ
language English
format Article
sources DOAJ
author Yannan Liu
Sharon Shui Yee Leung
Yong Huang
Yatao Guo
Ning Jiang
Puyuan Li
Jichao Chen
Rentao Wang
Changqing Bai
Zhiqiang Mi
Zhancheng Gao
spellingShingle Yannan Liu
Sharon Shui Yee Leung
Yong Huang
Yatao Guo
Ning Jiang
Puyuan Li
Jichao Chen
Rentao Wang
Changqing Bai
Zhiqiang Mi
Zhancheng Gao
Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
Frontiers in Microbiology
Klebsiella pneumoniae
carbapenem resistance
capsular type
capsule depolymerase
antivirulence
author_facet Yannan Liu
Sharon Shui Yee Leung
Yong Huang
Yatao Guo
Ning Jiang
Puyuan Li
Jichao Chen
Rentao Wang
Changqing Bai
Zhiqiang Mi
Zhancheng Gao
author_sort Yannan Liu
title Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
title_short Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
title_full Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
title_fullStr Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
title_full_unstemmed Identification of Two Depolymerases From Phage IME205 and Their Antivirulent Functions on K47 Capsule of Klebsiella pneumoniae
title_sort identification of two depolymerases from phage ime205 and their antivirulent functions on k47 capsule of klebsiella pneumoniae
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2020-02-01
description Carbapenem-resistant Klebsiella pneumoniae (CRKP) pose a significant threat to global public health. In present research, a total of 80 CRKP strains belonging to ST11 were collected with 70% (56 of 80 isolates) expressing a K47 capsular type. Thus, it is significant to prevent and control infections caused by these bacteria. Capsule depolymerases could degrade bacterial surface polysaccharides to reduce their virulence and expose bacteria to host immune attack. Previous studies have demonstrated the potential of phage-encoded depolymerases as antivirulent agents in treating CRKP infections in vitro and in vivo. Here, two capsule depolymerases (Dpo42 and Dpo43) derived from phage IME205 were expressed and characterized. Although both depolymerases act on strains with a capsular serotype K47, they are active against different subsets of strains, indicating subtle differences in capsule composition that exist within this serotype. The host range of phage IME205 matched to the sum of specificity range of Dpo42 and Dpo43. These two enzymes maintained stable activity in a relatively broad range of pH levels (pH 5.0–8.0 for Dpo42 and pH 4.0–8.0 for Dpo43) and temperatures (20–70°C). Besides, both Dpo42 and Dpo43 could make host bacteria fully susceptible to the killing effect of serum complement and display no hemolytic activity to erythrocytes. In summary, capsule depolymerases are promising antivirulent agents to combat CRKP infections.
topic Klebsiella pneumoniae
carbapenem resistance
capsular type
capsule depolymerase
antivirulence
url https://www.frontiersin.org/article/10.3389/fmicb.2020.00218/full
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