ORIGINAL RESEARCH article

Front. Public Health, 01 September 2021
Sec. Infectious Diseases – Surveillance, Prevention and Treatment
https://doi.org/10.3389/fpubh.2021.724212

An Outbreak of Carbapenem-Resistant Klebsiella pneumoniae of K57 Capsular Serotype in an Emergency Intensive Care Unit of a Teaching Hospital in China

Chunhong Shao1, Yan Jin1, Wei Wang2, Meijie Jiang3* and Shuping Zhao3*
  • 1Clinical Laboratory of Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China
  • 2Intensive Care Department of Taian City Central Hospital, Tai'an, China
  • 3Clinical Laboratory of Taian City Central Hospital, Tai'an, China

The emergence of carbapenem-resistant hypervirulent K. pneumoniae (CR-hvKP) strains has increased the threat posed by K. pneumoniae. Here, we described an outbreak of 32 CR-hvKP isolates from the emergency intensive care unit (EICU) of a teaching hospital in China. Thirty-two CRKp isolates were collected from six patients and their surrounding environment in EICU. Antimicrobial susceptibility testing was performed using VITEK 2 compact system, E-test or the broth microdilution method. All isolates were serotyped, antimicrobial resistance genes and virulence-associated genes were screened using PCR. Multilocus sequence typing (MLST) and pulse-field gel electrophoresis (PFGE) were employed to characterize the genetic relationships among the CPKP isolates. The virulence capability of 11 CRKp isolates from six patients was evaluated through Galleria mellonella larva infection assay. PFGE showed that all 32 isolates belonged to one cluster, and MLST revealed that belonged to ST11. All isolates exhibited high resistance to β-lactam antibiotics, quinolones, and aminoglycosides. They were susceptible to ceftazidime/averbatan, tigecycline, and colistin. All 32 isolates harbored blaKPC−2, blaSHV−11, blaTEM−1, rmtB, and qnrD. The serotype of all 32 isolates was K57. All 32 isolates contained 6 virulence genes, namely, fimH, iucB, mrkD, rmpA, uge, and wabG. Infection assays demonstrated high mortality in the Galleria mellonella model. Following measures implemented by the hospital, the outbreak was controlled. The mortality rate was 50.0%. The epidemiology of CR-hvKP should be monitored closely to detect early indications of this emerging public health threat.

Introduction

Klebsiella pneumoniae is a common causative pathogen of various nosocomial infections, including pneumonia, urinary tract infection, abdominal infection, and bacteremia. K. pneumoniae is now recognized as an urgent threat to human health because of the emergence of multidrug-resistant strains associated with hospital outbreaks and hypervirulent strains associated with severe community-acquired infections (1). Surveillance of antibiotic resistance by CHINET in China showed that 4.9 and 4.8% of K. pneumoniae strains were resistant to imipenem and meropenem, respectively, in 2009, compared with 25.3 and 26.8%, respectively, in 2019 (http://chinets.com/Data/GermYear). Infections caused by carbapenem-resistant K. pneumoniae (CRKp) have few treatment options and are associated with mortality rates upwards of 50% (2). Several mechanisms are responsible for the carbapenem-resistance of K. pneumoniae, among which, carbapenemase production remains the most clinically relevant (3).

Over the past two decades, the newly emerged hypervirulent K. pneumoniae (hvKP) strain has caused great concern globally. HvKp is an evolving pathotype that is more virulent than classical K. pneumoniae (cKP). HvKP usually infects healthy individuals from the community. Infections are more common in the Asian but are occurring globally (4). Unlike cKP, hvKP is rarely resistant to commonly used antimicrobial agents, except for an intrinsic resistance to ampicillin (5). The distinct virulence determinants of hvKp include iron acquisition, increased capsule production, K1 and K2 capsule types, and the colibactin toxin (6). The ability to acquire iron is essential for bacterial growth and the progression of infection. iucABCD, which encodes for aerobactin and its cognate receptor, is more prevalent in hvKP than cKP (7). Additionally, hvKp strains demonstrate hypermucoviscosity, a phenotypic description of hvKp in laboratory conditions that has become a distinguishing feature of many hypervirulent isolates (6).

Along with the global dissemination of mobile genetic elements conferring antibiotic resistance, antibiotic-resistant hvKP isolates, especially carbapenem-resistant hvKP (CR-hvKP), have attracted increasingly more attention and have been increasingly reported worldwide (5). In China, several outbreaks of CR-hvKP have been reported (810). blaKPC−2 is the predominant carbapenemase in both CRKp and CR-hvKp (11, 12). ST11 is the major sequence type of CR-hvKp from Asia, especially China (13). Here, we have described an outbreak of CR-hvKP with 32 isolates from the emergency intensive care unit (EICU) of Taian City Central Hospital, Shandong, China. We sought to investigate the molecular and epidemiological features of these isolates during the outbreak, especially the characteristics of antimicrobial resistance determinants and virulence factors.

Materials and Methods

Patients and CRKp Isolates From EICU

From January 29, 2019 to March 11, 2019, six patients with CRKp infection were found in EICU. A total of 11 CRKps were isolated from their blood, sputum, and bronchoalveolar lavage fluid (BALF). Patient information including age, gender, length of EICU stay, diagnosis, treatment, and outcomes were obtained from electronic medical records. The methods used in this study were approved by the Ethics Committee of Taian City Central Hospital and were carried out in accordance with the approved guidelines. On February 10 and February 20, 2019, the hospital environment of six patients was sampled and 21 CRKp isolates were obtained from the patients' environment in the hospital, including bed sheets, pillows, sphygmomanometers, ventilators, tables, mice, keyboards, and the hands of medical staff. The 32 isolates were identified as K. pneumoniae using Vitek-MS system (BioMérieux, France). Phenotypic detection of carbapenemases was performed using carbapenem inactivation method (CIM) and EDTA-modified CIM (eCIM) test according to the approved standard of the Clinical and Laboratory Standards Institute 2020 guidelines (14).

Determination of Hypermucoviscosity Phenotype

The hypermucoviscosity phenotype was determined by the “string test.” Samples were cultured on agar plates overnight at 37°C. Then, a colony from the plate was stretched with a bacteriology loop. If a viscous string over 5 mm in length forms, it is considered to be a positive result.

Antibiotic Susceptibility Assay

Antimicrobial susceptibility testing was performed using VITEK 2 compact system (BioMérieux, France). The minimum inhibitory concentrations (MICs) of imipenem, meropenem, and ertapenem were determined through an E-test (BioMérieux, France). The MICs of tigecycline and colistin were determined using the broth microdilution method (Bio-kont, China). The antimicrobial susceptibility of ceftazidime/averbatan was determined using Kirby-Bauer test (Oxide, America). Escherichia coli ATCC25922 and K. pneumoniae ATCC700603 served as the quality controls. All antibiotics were administered according to the approved standard of the 2020 European Committee on Antimicrobial Susceptibility Testing breakpoint (www.eucast.org/clinical-breakpoint).

PCR and DNA Sequence Analysis of Drug Resistance Genes, Serotype, and Virulence Genes

As described previously, a variety of antimicrobial resistance genes were screened using PCR and DNA sequencing (15). These genes included carbapenem resistance genes (blaKPC, blaSME, blaIMI, blaNMC, blaGES, blaIMP, blaVIM, blaGIM, blaSIM, blaSPM, blaNDM, and blaOXA−48like), other β-lactamase genes (blaCTX−M, blaTEM, blaSHV, blaMOX, blaFOX, blaDHA, blaCIT, and blaEBC), plasmid-mediated quinolone resistance genes [qnrA, qnrB, qnrC, qnrD, qnrS, qepA, and aac (6)-Ib-cr], and 16S rRNA methyase gene (rmtA, rmtB, rmtC, rmtD, npmA, and armA). The positive PCR products were sequenced by Beijing Genomics Institute Technology Co. Ltd. Sequence alignments were completed by running BLAST at NCBI website (http://blast.ncbi.nlm.nih.gov/Blast.cgi). Subsequently, the isolates were serotyped for K1, K2, K5, K20, K54, and K57 serotypes, and twelve virulence-associated genes, including rmpA, aerobactin, wcaG, ybtA, iucB, iroNB, ureA, uge, kfuBC, fim, wabG, and allS, were screened using PCR, as previously described (15).

Multilocus Sequence Typing

MLST of K. pneumoniae was performed according to protocols available on the MLST Pasteur website (http://www.pasteur.fr/recherche/genopole/PF8/mlst/Kpneumoniae.html). Seven conserved housekeeping genes (gapA, infB, mdh, pgi, phoE, rpoB, and tonB) were amplified, sequenced, and compared with those in the MLST databases.

Pulse-Field Gel Electrophoresis

An overnight bacterial culture was suspended in cell suspension buffer [100 mM EDTA, 100 mM Tris-HCl (pH 8.0)] and adjusted to an optical density of 4.0 at the wave length of 600 nm. The suspension was mixed with equal volume of 2% solution of low-melting agarose in Tris-EDTA [TE: 1 mM EDTA, 10 mM Tris-HCl (pH 8.0)]. After cooling, the agarose sections were incubated for 4 h at 54°C in cell lysis buffer [50 mM Tris-HCl, 50 mM EDTA (pH 8.0), 0.01 g/mL N-lauroyl-sarcosine, sodium salt, 0.1 mg/mL proteinase K]. They were then washed thoroughly with TE buffer and digested overnight with XbaI restriction endonuclease (Takara Bio, Inc., Otsu, Japan). Genomic DNA separation was performed in 0.5 X Tris/borate/EDTA (TBE) buffer in a PFGE system (CHEF Mapper; Bio-Rad Laboratories, Inc., Hercules, CA, USA) at 14°C, using a voltage of 6 V/cm, a switch angle of 120° and a switch ramp of 6–36 s for 19 h. The Salmonella enterica serotype Braenderup H9812 was used as a marker for PFGE.

Galleria Mellonella Larva Infection Assay

The virulence capability of 11 CRKp isolates from six patients was evaluated through a commonly used in vivo infection model, the wax moth G. mellonella (8). In the present study, each infection group included 10 larvae. Larvae were injected with 10 μL of bacterial suspension at a concentration of 106 CFU per larva. As a control group, 10 μL PBS was injected in parallel. All larvae were placed in petri-dishes and kept at 37°C in the dark. At 24, 48, 72, and 96 h after injection, the number of dead larvae was recorded with notes on any melanization and lack of motility. All experiments were performed with biological triplicates and results were not considered if two or more larvae in any of the control groups died.

Results

Outbreak Description

From January 29 to March 11, 2019, six patients admitted to EICU were included in this analysis. The age of patients ranged from 54 to 87 years and the patients were admitted to EICU due to Chronic obstructive pulmonary disease (COPD), severe pneumonia, cerebral infarction, and septic shock. They all showed the typical symptoms of pulmonary edema, excessive sputum, pleural effusion, and shortness of breath (Table 1). All six patients received traumatic and/or antibiotic treatment during their hospitalization in the EICU (Figure 1). The antibiotics used mainly included carbapenems, cefoperazone/sulbactam, piperacillin/tazobactam, quinolones, and tigecycline. In addition, patient 2 was treated with voriconazole.

TABLE 1
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Table 1. Clinical characteristics of six patients with CRKp infection in EICU.

FIGURE 1
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Figure 1. Epidemiology of the CR-hvKP outbreak cases. Each horizontal line represents the timeline of one patient, with the abscissa axis showing the relevant dates. The isolates from different specimens and the traumatic treatment of these patients are represented by “□” and “Δ,” respectively. The outcome of the patients was represented by “O,” and the antibiotics used were represented by different color lines, and the length of the color lines represented the length of the antibiotic use.

On February 3, 2019, the first two CRKp isolates were isolated from the sputum of patient 4 and patient 2, respectively. Patient 4 was the first patient to be admitted to EICU. Subsequently, CRKps were also isolated from blood samples or BALF of these two patients. So on February 10, the hospital environment of patient 2 and patient 4 was sampled and their rooms were thoroughly disinfected with glutaraldehyde. However, in the next 10 days, another 4 patients were continuously confirmed to have CPKp infection in the ECU. Among them, patient 1 was admitted to EICU as early as February 3, and the other three patients were admitted after February 10. Therefore, an overlap period between patient 1 and patient 2, patient 4 was observed. So on February 20, the hospital environment of patient 1, patient 3, patient 5, and patient 6 was sampled and their rooms were thoroughly disinfected with glutaraldehyde.

In order to control the outbreak, the staffs of EICU were trained and educated in environmental disinfection and carrying out hand hygiene in a timely and effective manner. Eventually, the epidemic situation was effectively controlled. Except for these 6 patients, no other infected patients have been found in EICU to date. Finally, two patients improved and was discharged, three patients died during treatment in hospital. The survival time of patient 3 was the shortest after CRKp isolation, which was only 3 days. One gave up treatment. The mortality rate was 50.0%.

Drug Resistance and Resistance Genes of CRKp Isolates

The antimicrobial susceptibility profiles of the 32 CRKp isolates are listed in Supplementary Table 1. All isolates exhibited high resistance to aztreonam, cephalosporin, β-lactam/β-lactamase inhibitor combinations, carbapenems, quinolones, and aminoglycosides. Seven isolates (21.88%, 7/32) were resistant to trimethoprim-sulfamethoxazole. All isolates were susceptible to colistin, tigecycline, and ceftazidime/averbatan (100%). All strains were positive for MCIM test and negative for eCIM test.

For the resistance to β-lactams, all 32 isolates carried the blaKPC−2, blaSHV−11, and blaTEM−1 genes (Table 2). In addition, 27 isolates carried blaCTX−14 gene, and 3 isolates (Kp15, Kp16, and Kp17) from the hospital environment of patient 3 carried blaCTX−14 and blaCTX−15 simultaneously. For aminoglycoside resistance, all isolates carried rmtB, and three isolates also carried armA. In addition, all 32 isolates carried qnrD, which may have led to quinolone resistance.

TABLE 2
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Table 2. The drug-resistance genes and virulence genes of 32 CR-hvKP.

Serotype and Virulence of CRKp Isolates

The string test of 32 isolates showed negative results. The serotype of all 32 isolates was K57. In the virulence gene analysis, all 32 isolates were found to contain 6 virulence genes, including fimH, iucB, mrkD, rmpA, uge, and wabG (Table 2).

We infected G. mellonella larvae with 11 CRKp isolates obtained from clinical specimens of the six patients. Kp1 and Kp11 from patient 1 were the least toxic, with 20% of larvae surviving after 96 h. All larvae infected by the other nine strains died within 96 h. Kp3 from patient 3 was the most toxic. The 24- and 48-h survival rates of larvae infected with Kp3 were 40 and 20% respectively, and all larvae died within 72 h. The results are shown in Figure 2.

FIGURE 2
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Figure 2. Eleven CR-hvKP isolates from six patients infection of G. mellonella larvae induces time-dependent lethality. The G. mellonella larvae injected with PBS were used as control.

MLST and PFGE Analysis of CRKp Isolates

MLST analysis revealed that all 32 CRKp isolates were of the ST11 type, which is the most common type of CRKp found in China. The results of PFGE showed that the homology of 32 isolates was more than 80%, indicating that they were a cluster. With the exception of Kp5, Kp21, Kp22, and Kp30, the homology of other 28 isolates was higher than 91.8%. Furthermore, three isolates (Kp5, Kp21, and Kp22) from patient 5 and four isolates (Kp1, Kp12, Kp13, and Kp14) from patient 1 showed complete homology (Figure 3).

FIGURE 3
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Figure 3. PFGE results and MLST typing for 32 CR-hvKP isolates. Green represents strains isolated from clinical specimens of six patients; purple represents strains isolated in hospital environment on February 10, 2019; and orange represents strains isolated in hospital environment on February 20, 2019. “O” represents strains isolated from hands of cleaner in EICU.

Discussion

K. pneumoniae is widely recognized as a pathogen with a propensity for acquiring antibiotic resistance. It is capable of causing a range of hospital-acquired infections and community-acquired invasive infections (16). The appearance of CR-hvKP makes this bacterium more threatening. Here we described a nosocomial outbreak of CR-hvKP in the EICU of a teaching hospital. This outbreak involved six patients and lasted for 40 days. Thirty-two CR-hvKp were isolated from six patients and their surrounding environment. These six patients did not share one ward and did not share medical equipments. However, PFGE showed that all 32 CR-hvKp isolates belonged to one cluster. Hospital monitoring showed that this outbreak of CRKp might have been caused due to the contaminated hands of cleaners. The hospital took positive measures and the outbreak was controlled. Therefore, in order to prevent the spread and prevalence of multidrug-resistant bacteria, timely submission of specimens, and detection of multi-drug resistant bacteria are very important in addition to disinfection, isolation, and treatment (17). Previous and this study showed that K. pneumoniae could survive on hospital equipment and hands of medical staff that had undergone rigorous cleaning. It is suggested that K. pneumoniae has a high degree of environmental stability under some circumstances and indicates that decontamination should be verified after the cleaning process (2).

The capsule polysaccharide of K. pneumoniae has long been viewed as an important virulence factor that promotes resistance to phagocytosis and serum bactericidal activity. To date, more than 100 capsular (K) serotypes of K. pneumoniae have been identified (18). Notably, many reports have shown that K1 and K2 serotypes are strongly associated with hvKP (19, 20). Nevertheless, serotype K57 has also been considered as one of the pyogenic liver abscess-associated capsular types that are rarely reported (21, 22). In 2020, Wei et al. studied 39 K57 K. pneumoniae isolates. Among them, ST412 was the most prevalent, and all isolates harbored blaKPC−2 (22). In the present study, we identified that all 32 CR-hvKP isolates belonged to K57 and ST11. To our knowledge, this is the first report of K57 and ST11 K. pneumoniae with carbapenem resistance associated with clinical infection.

Several virulence factors have been suggested to contribute to the pathogenesis of hvKP strains. To date, rmpA and magA are the most frequently reported factors that have direct correlation with hvKP virulence (23). RmpA is located either on the chromosome or on a large virulence plasmid. The correlation between rmpA and hypermucoviscosity is very high, and the presence of rmpA among a set of genes has been proposed as biomarker to identify potential hvKp strains (24). However, in this study, all 32 hypermucoviscosity-negative isolates were positive for rmpA and a previous study reported similar results (22). The underlying reason may be that rmpA cannot work alone, or there may be a mutation of rmpA. In addition, a correlation between the presence of rmpA and aerobactin has been described, wherein 96% of rmpA positive isolates coproduced aerobactin (13). In this study, all 32 isolates were aerobactin producers.

In addition, the 32 isolates expressed four other virulence genes, including fimH, mrkD, uge, and wabG. FimH and mrkD encode type I and type III fimbriae, respectively. Fimbriae allow bacteria to attach to the host cells to establish infection. A previous report confirmed observations that type III fimbriae contribute to biofilm formation, and demonstrated that the expression of type III fimbriae is positively correlated with iron concentration (7). In this study, capsule-associated genes uge and wabG were detected in 32 isolates simultaneously. A previous study showed that the deletion of genes for capsule synthesis decreased the virulence of K. pneumoniae to varying degrees (25). In the absence of the gene uge, K. pneumoniae is less capable of causing urinary tract infections, pneumonia, and sepsis (26). In general, the serotype of the 32 isolates was K57, and their virulence genes were the same. However, the virulence test performed by infecting G. mellonella larvae showed that the virulence of 11 isolates from six patients was different, and their virulence was closely related to the survival time of the patients.

All CR-hvKP isolates in the present study were blaKPC−2-producing ST11 K. pneumoniae. In addition to blaKPC−2, all 32 isolates harbored blaSHV−11 and blaTEM−1. This is similar to previous reports (8, 10). These resistance genes lead to the resistance to β-lactams in the isolates. It should be noted that the drug resistance genes carried by several isolates from the environment are slightly different from isolates from patients. For example, Kp15, Kp16 and Kp17 isolated from the environment of patient 3 carry two ESBL genes at the same time. Therefore, it is considered that CRKp may lose or acquire drug resistance genes in the process of transmission. Furthermore, all isolates were resistant to aminoglycosides and quinolones, which severely limited the clinical choice of antibiotics. Fortunately, all strains were sensitive to tigecycline, colistin and ceftazidime/averbatan. Finally, two patients recovered and was discharged, three patients died, and the mortality rate was 50.0%. This is higher than that described in previous reports (5, 26).

Conclusions

We described an outbreak of ST11 K. pneumoniae, which exhibited hypervirulence and carbapenem resistance, in EICU of a teaching hospital in China. The serotype of all 32 isolates was K57. This report confirmed that CR-hvKP can be transmitted nosocomially through the surrounding environment of the hospital. Hence, monitoring the nosocomial dissemination of CR-hvKP is essential for its prevention and outbreak management.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by the Ethics Committee of Taian City Central Hospital. The patients/participants provided their written informed consent to participate in this study. The animal study was reviewed and approved by the Ethics Committee of Taian City Central Hospital.

Author Contributions

CS carried out the experiments and wrote the paper. YJ performed the results analysis. WW collected clinical information of patients. MJ and SZ designed the experiments and revised the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by the National Natural Science Foundation of China (no. 81401696) and the Shandong Provincial Natural Science Foundation of China (no. ZR2016HL44).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2021.724212/full#supplementary-material

Abbreviations

cKP, classical K. pneumoniae; CRKp, carbapenem-resistant K. pneumoniae; hvKP, hypervirulent K. pneumoniae; CR-hvKP, carbapenem-resistant hypervirulent K. pneumoniae; EICU, emergency intensive care unit; BALF, bronchoalveolar lavage fluid; MLST, multilocus sequence typing; PCR, polymerase chain reaction; PFGE, pulse-field gel electrophoresis.

References

1. Holt KE, Wertheim H, Zadoks RN, Baker S, Whitehouse CA, Dance D, et al. Genomic analysis of diversity, population structure, virulence, and antimicrobial resistance in Klebsiella pneumoniae, an urgent threat to public health. Proc Natl Acad Sci USA. (2015) 112:E3574–81. doi: 10.1073/pnas.1501049112

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Snitkin ES, Zelazny AM, Thomas PJ, Stock F, NISC Comparative Sequencing Program Group, Henderson DK, et al. Tracking a hospital outbreak of carbapenem-resistant Klebsiella pneumoniae with whole-genome sequencing. Sci Transl Med. (2012) 4:148ra116. doi: 10.1126/scitranslmed.3004129

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Pitout JD, Nordmann P, Poirel L. Carbapenemase-producing Klebsiella pneumoniae, a key pathogen set for global nosocomial dominance. Antimicrob Agents Chemother. (2015) 59:5873–84. doi: 10.1128/AAC.01019-15

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Russo TA, Marr CM. Hypervirulent Klebsiella pneumoniae. Clin Microbiol Rev. (2019) 32:e00001–19. doi: 10.1128/CMR.00001-19

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Lee CR, Lee JH, Park KS, Jeon JH, Kim YB, Cha CJ, et al. Antimicrobial resistance of hypervirulent Klebsiella pneumoniae: epidemiology, hypervirulence-associated determinants, and resistance mechanisms. Front Cell Infect Microbiol. (2017) 7:483. doi: 10.3389/fcimb.2017.00483

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Choby JE, Howard-Anderson J, Weiss DS. Hypervirulent Klebsiella pneumoniae- clinical and molecular perspectives. J Intern Med. (2020) 287:283–300. doi: 10.1111/joim.13007

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Shon AS, Bajwa RP, Russo TA. Hypervirulent (hypermucoviscous) Klebsiella pneumoniae: a new and dangerous breed. Virulence. (2013) 4:107–18. doi: 10.4161/viru.22718

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Zhao Y, Zhang X, Torres V, Liu H, Rocker A, Zhang Y, et al. An outbreak of carbapenem-resistant and hypervirulent Klebsiella pneumoniae in an intensive care unit of a major teaching hospital in Wenzhou, China. Front Public Health. (2019) 7:229. doi: 10.3389/fpubh.2019.00229

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Yao B, Xiao X, Wang F, Zhou L, Zhang X, Zhang J. Clinical and molecular characteristics of multi-clone carbapenem-resistant hypervirulent (hypermucoviscous) Klebsiella pneumoniae isolates in a tertiary hospital in Beijing, China. Int J Infect Dis. (2015) 37:107–12. doi: 10.1016/j.ijid.2015.06.023

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Zhan L, Wang S, Guo Y, Jin Y, Duan J, Hao Z, et al. Outbreak by hypermucoviscous Klebsiella pneumoniae ST11 isolates with carbapenem resistance in a tertiary hospital in China. Front. Cell. Infect. Microbiol. (2017) 7:182. doi: 10.3389/fcimb.2017.00182

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Gu B, Bi R, Cao X, Qian H, Hu R, Ma P. Clonal dissemination of KPC-2-producing Klebsiella pneumoniae ST11 and ST48 clone among multiple departments in a tertiary teaching hospital in Jiangsu Province, China. Ann Transl Med. (2019) 7:716. doi: 10.21037/atm.2019.12.01

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Xu M, Fu Y, Fang Y, Xu H, Kong HS, Liu YC, et al. High prevalence of KPC-2-producing hypervirulent Klebsiella pneumoniae causing meningitis in Eastern China. Infect Drug Resist. (2019) 12:641–53. doi: 10.2147/IDR.S191892

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Remya PA, Shanthi M, Sekar U. Characterisation of virulence genes associated with pathogenicity in Klebsiella pneumoniae. Indian J Med Microbiol. (2019) 37:210–8. doi: 10.4103/ijmm.IJMM_19_157

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing Twentieth Informational Supplement. Wayne, PA: CLSI (2020).

15. Shao C, Wang W, Liu S, Zhang Z, Jiang M, Zhang F. Molecular epidemiology and drug resistant mechanism of carbapenem-resistant Klebsiella pneumoniae in elderly patients with lower respiratory tract infection. Front Public Health. (2021) 9:669173. doi: 10.3389/fpubh.2021.669173

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Palacios M, Miner TA, Frederick DR, Sepulveda VE, Quinn JD, Walker KA, et al. Identification of two regulators of virulence that are conserved in Klebsiella pneumoniae classical and hypervirulent strains. mBio. (2018) 9:e01443–18. doi: 10.1128/mBio.01443-18

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Vock I, Tschudin-Sutter S. Persisting intrahospital transmission of multidrug-resistant Klebsiella pneumoniae and challenges for infection control. Infect Control Hosp Epidemiol. (2019) 40:904–9. doi: 10.1017/ice.2019.153

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Wyres KL, Wick RR, Gorrie C, Jenney A, Follador R, Thomson NR, et al. Identification of Klebsiella capsule synthesis loci from whole genome data. Microb Genom. (2016) 2:e000102. doi: 10.1099/mgen.0.000102

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Zhang Y, Zhao C, Wang Q, Wang X, Chen H, Li H, et al. High prevalence of hypervirulent Klebsiella pneumoniae infection in china: geographic distribution, clinical characteristics, and antimicrobial resistance. Antimicrob Agents Chemother. (2016) 60:6115–20. doi: 10.1128/AAC.01127-16

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Catalán-Nájera JC, Garza-Ramos U, Barrios-Camacho H. Hypervirulence and hypermucoviscosity: two different but complementary Klebsiella spp. phenotypes? Virulence. (2017) 8:1111–23. doi: 10.1080/21505594.2017.1317412

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Hsu CR, Liao CH, Lin TL, Yang HR, Yang FL. Identification of a capsular variant and characterization of capsular acetylationin Klebsiella pneumoniae PLA-associated type K57. Sci Rep. (2016) 6:31946. doi: 10.1038/srep31946

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Wei DD, Xiong XS, Mei YF, Du FL, Wan LG, Liu Y. Microbiological and clinical characteristics of Klebsiella pneumoniae isolates of K57 capsular serotype in China. Microb Drug Resist. (2021) 27:391–400. doi: 10.1089/mdr.2018.0456

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Rastegar S, Moradi M, Kalantar-Neyestanaki D, Ali Golabi D, Hosseini-Nave H. Virulence factors, capsular serotypes and antimicrobial resistance of hypervirulent Klebsiella pneumoniae and classical Klebsiella pneumoniae in Southeast Iran. Infect Chemother. (2019). doi: 10.3947/ic.2019.0027

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Walker KA, Miller VL. The intersection of capsule gene expression, hypermucoviscosity and hypervirulence in Klebsiella pneumoniae. Curr Opin Microbiol. (2020) 54:95–102. doi: 10.1016/j.mib.2020.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Pan PC, Chen HW, Wu PK, Wu YY, Lin CH, Wu JH. Mutation in fucose synthesis gene of Klebsiella pneumoniae affects capsule composition and virulence in mice. Exp Biol Med. (2011) 236:219–26. doi: 10.1258/ebm.2010.010193

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Gu D, Dong N, Zheng Z, Lin D, Huang M, Wang L, et al. A fatal outbreak of ST11 carbapenem-resistant hypervirulent Klebsiella pneumoniae in a Chinese hospital: a molecular epidemiological study. Lancet Infect Dis. (2018) 18:37–46. doi: 10.1016/S1473-3099(17)30489-9

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Keywords: Klebsiella pneumoniae, K57, hypervirulent, carbapenem-resistant, outbreak, China

Citation: Shao C, Jin Y, Wang W, Jiang M and Zhao S (2021) An Outbreak of Carbapenem-Resistant Klebsiella pneumoniae of K57 Capsular Serotype in an Emergency Intensive Care Unit of a Teaching Hospital in China. Front. Public Health 9:724212. doi: 10.3389/fpubh.2021.724212

Received: 12 June 2021; Accepted: 09 August 2021;
Published: 01 September 2021.

Edited by:

Jessica L. Jones, United States Food and Drug Administration, United States

Reviewed by:

Jiabin Li, Anhui Medical University, China
Farzaneh Firoozeh, Alborz University of Medical Sciences, Iran
Dóra Paróczai, University of Szeged, Hungary

Copyright © 2021 Shao, Jin, Wang, Jiang and Zhao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Meijie Jiang, xtingw@126.com; Shuping Zhao, dczhshp@126.com

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