Anti-restriction protein ArdA promotes clinical Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae spread and its molecular mechanism

Author:

Chen Huimin1,Tao Shuan1,Li Na2,Zhu Qing3,Liu Liping3,Fang Yeiwei4,Xu Yao4,Liang Wei5ORCID

Affiliation:

1. School of Medicine, Jiangsu University , Zhenjiang, Jiangsu , China

2. Laboratory Medical School, Bengbu Medical College , Bengbu, Anhui , China

3. School of Medicine, Xuzhou Medical University , Xuzhou, Jiangsu , China

4. School of medicine, Ningbo University , Ningbo, Zhejiang , China

5. Department of Clinical Laboratory, Ningbo First Hospital, Ningbo , No. 59, Liuting Street, Ningbo City, Zhejiang 315010 , China

Abstract

Abstract Background Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae (KPC-KP) has spread worldwide and has become a major threat to public health. The restriction modification system provides an innate defence of bacteria against plasmids or transposons, while many different types of plasmid encoding the anti-restriction protein ArdA can specifically affect the restriction activity in bacteria. Objectives To detect the codistribution of ArdA and blaKPC-2 plasmids in KPC-KP and explore the molecular mechanism of ArdA promoting KPC-KP spread. Methods We collected 65 clinical CRKP isolates from Ningbo, China, and 68 cases of plasmid complete sequences in GenBank to determine the prevalence of ArdA gene on the K. pneumoniae blaKPC-2 plasmid. The anti-restriction function of ArdA in promoting horizontal gene transfer (HGT) was verified by transformation, conjugation and transduction methods, and the pull-down experiment was used to investigate the molecular mechanism of ArdA protein in vitro. Results We found that ArdA was widely distributed in KPC-KP in 100% of cases, which was detected in 0% of drug susceptible K. pneumoniae, and the plasmids containing the ArdA gene in 90% of the 30 cases randomly retrieved from the database. We also verified that ArdA has a good anti-restriction function (P < 0.05) through two aspects of HGT (transformation, transduction), and explored the non-occurrence interaction of ArdA and the hsdM subunit protein of EcoKI enzyme from the perspective of protein molecules. Conclusions These findings suggest that the coexistence advantage of ArdA with the blaKPC-2 plasmids may provide KPC-producing K. pneumoniae with a very efficient evasion of the restriction of type I systems, which not only favours ArdA-containing mobile genetic elements in the same species HGT between bacteria also facilitates HGT between other bacterial species.

Funder

Natural Science Foundation of Jiangsu Province

Scientific Research Project in Jiangsu Province

Jiangsu Commission of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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