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Pyogenic spondylitis caused by Klebsiella pneumoniae: should the possibility of hypervirulent Klebsiella pneumoniae be considered?

BMC Infectious Diseases volume 22, Article number: 801 (2022) Cite this article

Abstract

Background

Klebsiella pneumoniae is rare but the second most common causative agent among gram-negative bacteria that cause pyogenic spondylitis. However, there are no available studies on the serotype, virulence factors, and clinical characteristics associated with K. pneumoniae-caused pyogenic spondylitis. Accordingly, we investigated the clinical characteristics of pyogenic spondylitis, K1 and K2 serotypes, and virulence factors of K. pneumoniae.

Methods

We reviewed the microbiological reports of specimens collected between January 2014 and December 2019 as well as the medical records of patients with pyogenic spondylitis caused by K. pneumoniae. We also evaluated K1 and K2 serotypes and the virulent genes rmpA, iutA, mrkD, ybtS, entB, and kfu. Strains that possessed rmpA and iutA were defined as hypervirulent K. pneumoniae.

Results

Six patients with pyogenic spondylitis caused by K. pneumoniae were enrolled in the study. The capsular serotypes K1 and K2 were present in 66.7% (4/6) of cases, and the hypervirulent strains were present in 88.3% (5/6) of cases. All patients had community-acquired infections, and all strains isolated were susceptible to antimicrobial agents. Intravenous antibiotic treatment continued for 2–7 weeks, and no patient underwent decompressive operation or surgical debridement. There was no recurrence. One patient died from pneumonia with a septic lung.

Conclusion

Hypervirulent K. pneumoniae is a rare but possible causative agent associated with pyogenic spondylitis.

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Background

Recent years have seen a notable increase in cases of pyogenic spondylitis, especially in elderly populations [1,2,3]. This rise is attributable to various risk factors prevalent in this group, such as an increased frequency of immunodeficiency disorders and chronic diseases, and more frequent use of invasive spinal procedures [1,2,3]. The increased use of advanced diagnostic tools such as magnetic resonance imaging or bone scans have also contributed to improved early detection and diagnosis of the disease [2]. Pyogenic spondylitis is associated with a significant mortality rate and frequent relapse [4]. Patients with pyogenic spondylitis also suffer from residual disability, severe functional sequelae, and long-term antibiotic treatment [4].

The most common organism responsible for pyogenic spondylitis infections is Staphylococcus aureus [5]. The proportion of gram-negative organisms is 10–30%, compared to 60-80% of gram-positive bacteria [6,7,8,9,10]. Among the gram-negative bacteria, Escherichia coli is the most common, followed by Klebsiella pneumoniae, which accounts for 1–5% of all infections [6,7,8,9,10]. Intra-abdominal and urinary tract infections (UTIs) are the most common source of pyogenic spondylitis caused by gram-negative bacteria [8, 11].

K. pneumoniae present in a healthcare setting, known as “classic K. pneumoniae” (cKP), has been reported to be a main causative agent of pneumonia, UTI, and bloodstream infections in immunocompromised patients [12]. “Hypervirulent K. pneumoniae” (hvKP), in contrast, tends to be contracted in the community, cause more invasive or metastatic infections, including liver abscess, endophthalmitis, septic lung, osteomyelitis, pyomyositis, and necrotizing fasciitis, and is responsible for more of the infections observed in relatively healthy individuals [12]. To date, 79 capsular types have been identified and associated with various Klebsiella species, with the K1 and K2 serotypes known to be associated with hypervirulent features [13, 14]. One recent study showed that virulence genes, such as iroB, iucA, peg-344, rmpA, and rmpA2, closely correlate with or are determinant factors of hvKP [15].

K. pneumoniae is well-known for its role in pneumonia and other HCA infections [16], but comparatively less information is available concerning pyogenic spondylitis caused by K. pneumoniae of the K1 and K2 serotypes or possessing virulent genes. Therefore, we examined the clinical implications of pyogenic spondylitis caused by K. pneumoniae, as well as its microbiological features such as the K1 and K2 serotypes, and the virulence genes iutA, rmpA, ybtS, entB, kfu, mrkD, and allS.

Methods

Study setting and data collection

We conducted a retrospective study at a 1,200-bed tertiary hospital at Jeonbuk National University Hospital in Jeonju, Korea. We reviewed all medical records of patients aged ≥ 19 years who were diagnosed with pyogenic spondylitis, and identified all cases in which K. pneumoniae was isolated from blood cultures, tissue cultures, or pus cultures between January 2014 and December 2019. The data collected from each subject included demographic characteristics, clinical signs and symptoms, underlying comorbidities, microbiological data, radiographic findings, laboratory data, surgical treatment, and clinical outcomes. Diagnosis of pyogenic spondylitis was made according to clinical, radiological, and microbiological criteria [17].

Definition

Healthcare-associated infection (HCA) is defined as a K. pneumoniae infection that develops within 48 h of hospital admission in patients (a) hospitalized for two or more days in the preceding 90 days, (b) that received intravenous medication or home wound care in the previous 30 days, (c) that received of hemodialysis, or (d) that reside in a nursing home or long-term care facility [18]. A community-acquired infection is one that occurs in patients with no risk factors for HCA infection for whom the first positive culture for K. pneumoniae was identified within 48 h of admission [18]. A hospital-acquired infection is one that is diagnosed through a positive culture for K. pneumoniae over 48 h after admission [18].

The neurologic staging is defined as follows: stage 0, no pain; stage 1, back pain at the level of the involved spine; stage 2, radiating pain from the involved spine; stage 3, motor weakness, sensory deficit, and bladder and bowel dysfunction; and stage 4, paralysis [19]. Sequelae are defined as persisting pyogenic spondylitis-associated signs and symptoms that last at least 12 months after the completion of treatment [11].

Microbiological evaluation and antimicrobial susceptibility

All laboratory tests were performed consistent with routine clinical practice. For cultures, all samples were inoculated onto blood agar and MacConkey agar plates in a 35 °C incubator for 16 to 24 h. The BacT/Alert 3D system (bioMérieux, Durham, NC, USA) was used for blood cultures. The isolated bacteria were identified using a VitekMS system (BioMérieux, Hazelwood, MI, USA) and antimicrobial susceptibility tests were conducted using Vitek 2 AST 211 cards (BioMérieux, Marcy-l’Étoile, France) and interpreted using the VITEK 2 identification system [20]. Multiplex polymerase chain reaction was used to detect K1 and K2 capsular serotypes and virulence genes. Primer sets for magA (wzy-like polymerase specific to K1 capsular serotype), wzi (the gene specifying the K2 capsular serotype), and other virulence genes (ybtS, entB, allS, kfu, iutA, mrkD, and rmpA) have been described previously [21]. hvKP is considered detected when both rmpA and iutA genes are positive [13].

Results

Over the course of the study a total of six patients with pyogenic spondylitis caused by K. pneumoniae were identified; five males and one female (Table 1). The six patients ranged in age from 60 to 84 years. Among the underlying diseases, diabetes mellitus (DM) was confirmed in two of six patients while colon cancer was confirmed in one patient. All patients had community-acquired infections. The sources of infection included a UTI in one patient and a liver abscess in another. All patients had a neurologic staging of 1 or 2. The thoracic spine was involved in two patients while the lumbosacral spine was involved in four cases. Bacteremia was also detected in four patients. The intravenous administration of antimicrobial agents such as ceftriaxone, cefotaxime, ceftazidime, ciprofloxacin, and meropenem continued for between 2 and 7 weeks. After intravenous antibiotic treatment, oral fluoroquinolone was prescribed. No patient underwent decompressive operation or surgical debridement as a result of neurologic complications during antibiotic treatment. Sequalae were observed in two cases but there was no recurrence. Among the six cases, the K1 and K2 serotypes were observed in four cases while hypervirulent strains, which have rmpA and iutA, were found in five patients (Table 2). One patient died owing to aggravation of septic lung, he did not, however, have the hypervirulent strain or the K1 or K2 serotype. Antimicrobial susceptibility tests showed that all isolates were sensitive to all tested antibiotics (amikacin, ampicillin-sulbactam, aztreonam, cefazolin, cefepime, cefotaxime, cefoxitin, ceftazidime, ertapenem, gentamicin, levofloxacin, meropenem, piperacillin-tazobactam, and tigecycline).

Table 1 The clinical features of patients with pyogenic spondylitis caused by Klebsiella pneumoniae
Full size table
Table 2 The serotypes and virulent factors of Klebsiella pneumoniae
Full size table

Discussion

This study suggests that K. pneumoniae is a clinically rare but significant pathogen of pyogenic spondylitis. To our knowledge, this is the first study to investigate K1 and K2 serotypes and virulence factors of pyogenic spondylitis-causing K. pneumoniae. Of the six strains tested, four were K1 and K2 serotypes while five were hypervirulent strains, suggesting that most K. pneumoniae that causes pyogenic spondylitis is hvKP.

Consistent with other studies concluding that intra-abdominal infections and UTI predisposing factors for pyogenic spondylitis caused by gram-negative bacteria, the UTI in Case 4 and liver abscess in Case 6 were identified as presumed sources of pyogenic spondylitis [8, 11]. The primary location of vertebral involvement, the number of invaded vertebral bodies, and the rate of positive blood culture observed in these patients were consistent with previous studies [8, 11]. Although there is no officially-recognized recommended treatment period, 8 weeks has been suggested as appropriate to prevent recurrence [11]. In this study, the intravenous antibiotics used included ceftriaxone, cefotaxime, ceftazidime, ciprofloxacin, and meropenem. The period of intravenous antibiotic administration of was 2–7 weeks, after which oral fluoroquinolone was maintained. In no case was recurrence observed after the conclusion of treatment. Because fluoroquinolone has a high oral bioavailability and good penetration into bone tissue, oral fluoroquinolone may be a good therapeutic option for prolonged antibiotic therapy [11]. For infectious spondylitis caused by gram-negative bacteria, 49.2% of patients undergo surgical treatment, but in this study none of the patients underwent surgery during antibiotic treatment [11]. This antibiotics used in Park et al.‘s study were fluoroquinolone and third-generation cephalosporin, which are similar to the antibiotics used in our study [11].

No standard definition of hvKP has yet been established. Hypervirulence in K. pneumoniae can be defined as the ability of the organism to cause invasive infections in healthy adults through metastatic dissemination from a primary infection site [22]. Diverse virulence factors are associated with a hypervirulent phenotype [12], including the production of hypercapsule, lipopolysaccharide, siderophores, and fimbriae (pili) [12]. Hypervirulence as a phenomenon is not thought to be associated with a single gene, but rather appears to be the result of complex interactions between multiple genetic determinants [13, 22]. The aerobactin gene cluster iucABCD, aerobactin transporter iutA (biosynthetic genes for the siderophore aerobactin), and rmpA or rmpA2 (which trigger hypercapsule production) have been regarded as good diagnostic candidates for hypervirulence [13]. In our study, five of the six strains were hypervirulent based on this definition, and in each case the strain was the causative pathogen of the infectious spondylitis. Although we were limited by the small number of samples available for testing, our findings do suggest that the hypervirulent strain may be more associated with pyogenic spondylitis than the classic strain. A study that compares the frequency of hvKP and cKP-induced pyogenic spondylitis with a greater number of study subjects is needed to confirm this hypothesis.

K. pneumoniae is a well-known multidrug-resistant bacteria with emerging carbapenemase-producing strains. In contrast, hvKP remains susceptible to most clinically used antibiotics [12]. All six patients studied showed community-acquired infection, and each of the identified strains proved to be susceptible to all antimicrobial agents studied. However, the emergence of hvKP-producing extended spectrum beta-lactamase (ESBL) or carbapenemase has been reported [23, 24]. As a pyogenic spondylitis treatment, the administration of intravenous antibiotics or highly bioavailable oral agents is recommended to continue for longer than 6 weeks [25]. If hvKP strains producing ESBL or carbapenemase cause pyogenic spondylitis, the selection of antimicrobial agents available in these cases is very limited, and it is unlikely that those available would exert a sufficient therapeutic effect. Moreover, the treatment of multiple sites infected by hvKP, including metastatic infections, is a therapeutic challenge owing to the poor penetration of certain antimicrobial agents when used to treat pyogenic spondylitis [13]. Although ESBL or multidrug-resistant hvKP were reported neither in this study nor previous studies concerning pyogenic spondylitis, continuous surveillance is required.

This study had some limitations. Salmochelin (iroA gene cluster, iroBCDE) and peg-344 were recently reported to be significant virulent factors specific to hvKP, though these were not tested in this study [15] nor did we test for the presence of rmpA2. Another limitation was the small number of cases, though we note that all obtainable cases over a six-year period were included. Finally, we investigated only some virulence factors, and declined to explore any virulence factors through an animal study. While hypervirulence could be demonstrated easily in a mouse infection model or Galleria mellonella infection model, we were unable to perform these tests. We defined microbial hypervirulence exclusively by reference to the presence of virulence genes [26].

Conclusion

This study suggests that hvKP is a rare but possible causative agent associated with pyogenic spondylitis. Although K. pneumoniae infection constitutes a relatively minor proportion of all cases, its clinical importance should be evaluated through larger studies, as treatment can become more complicated when resistance to antimicrobial agents increases.

Availability of data and materials

The data that support the findings of this study ara available from the corresponding author upon reasonable request.

Abbreviations

cKP:

classic K. pneumonia

hvKP:

hypervirulent K. pneumonia

HCA:

healthcare-associated infection

UTI:

urinary tract infection

ESBL:

extended spectrum β lactamase

References

  1. Gouliouris T, Aliyu SH, Brown NM. Spondylodiscitis: update on diagnosis and management. J Antimicrob Chemother. 2010;65(Suppl 3):iii11–24.

    CAS  PubMed  Google Scholar 

  2. Cottle L, Riordan T. Infectious spondylodiscitis. J Infect. 2008;56(6):401–12.

    Article  PubMed  Google Scholar 

  3. Kehrer M, Pedersen C, Jensen TG, Lassen AT. Increasing incidence of pyogenic spondylodiscitis: a 14-year population-based study. J Infect. 2014;68(4):313–20.

    Article  PubMed  Google Scholar 

  4. Mylona E, Samarkos M, Kakalou E, Fanourgiakis P, Skoutelis A. Pyogenic vertebral osteomyelitis: a systematic review of clinical characteristics. Semin Arthritis Rheum. 2009;39(1):10–7.

    Article  CAS  PubMed  Google Scholar 

  5. Zimmerli W. Clinical practice. Vertebral osteomyelitis. N Engl J Med. 2010;362(11):1022–9.

    Article  CAS  PubMed  Google Scholar 

  6. Russo A, Graziano E, Carnelutti A, Sponza M, Cadeo B, Sartor A, Righi E, Bassetti M. Management of vertebral osteomyelitis over an eight-year period: The UDIPROVE (UDIne PROtocol on VErtebral osteomyelitis). Int J Infect diseases: IJID : official publication Int Soc Infect Dis. 2019;89:116–21.

    CAS  Google Scholar 

  7. Park KH, Cho OH, Lee JH, Park JS, Ryu KN, Park SY, Lee YM, Chong YP, Kim SH, Lee SO, et al. Optimal Duration of Antibiotic Therapy in Patients With Hematogenous Vertebral Osteomyelitis at Low Risk and High Risk of Recurrence. Clin Infect diseases: official publication Infect Dis Soc Am. 2016;62(10):1262–9.

    Article  CAS  Google Scholar 

  8. Kang SJ, Jang HC, Jung SI, Choe PG, Park WB, Kim CJ, Song KH, Kim ES, Kim HB, Oh MD, et al. Clinical characteristics and risk factors of pyogenic spondylitis caused by gram-negative bacteria. PLoS ONE. 2015;10(5):e0127126.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Chang WS, Ho MW, Lin PC, Ho CM, Chou CH, Lu MC, Chen YJ, Chen HT, Wang JH, Chi CY. Clinical characteristics, treatments, and outcomes of hematogenous pyogenic vertebral osteomyelitis, 12-year experience from a tertiary hospital in central Taiwan. J Microbiol Immunol Infect. 2018;51(2):235–42.

    Article  PubMed  Google Scholar 

  10. Kim NJ. Microbiologic Diagnosis of Pyogenic Spondylitis. Infect Chemother. 2021;53(2):238–46.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Park KH, Cho OH, Jung M, Suk KS, Lee JH, Park JS, Ryu KN, Kim SH, Lee SO, Choi SH, et al. Clinical characteristics and outcomes of hematogenous vertebral osteomyelitis caused by gram-negative bacteria. J Infect. 2014;69(1):42–50.

    Article  PubMed  Google Scholar 

  12. Paczosa MK, Mecsas J. Klebsiella pneumoniae: Going on the Offense with a Strong Defense. Microbiol Mol biology reviews: MMBR. 2016;80(3):629–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Russo TA, Marr CM. Hypervirulent Klebsiella pneumoniae. Clinical microbiology reviews 2019, 32(3).

  14. Pan YJ, Lin TL, Chen CT, Chen YY, Hsieh PF, Hsu CR, Wu MC, Wang JT. Genetic analysis of capsular polysaccharide synthesis gene clusters in 79 capsular types of Klebsiella spp. Sci Rep. 2015;5:15573.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Russo TA, Olson R, Fang CT, Stoesser N, Miller M, MacDonald U, Hutson A, Barker JH, La Hoz RM, Johnson JR. Identification of Biomarkers for Differentiation of Hypervirulent Klebsiella pneumoniae from Classical K. pneumoniae. Journal of clinical microbiology 2018, 56(9).

  16. Hwang JH, Handigund M, Hwang JH, Cho YG, Kim DS, Lee J. Clinical Features and Risk Factors Associated With 30-Day Mortality in Patients With Pneumonia Caused by Hypervirulent Klebsiella pneumoniae (hvKP). Ann Lab Med. 2020;40(6):481–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Eren Gök S, Kaptanoğlu E, Celikbaş A, Ergönül O, Baykam N, Eroğlu M, Dokuzoğuz B. Vertebral osteomyelitis: clinical features and diagnosis. Clin Microbiol infection: official publication Eur Soc Clin Microbiol Infect Dis. 2014;20(10):1055–60.

    Article  Google Scholar 

  18. Friedman ND, Kaye KS, Stout JE, McGarry SA, Trivette SL, Briggs JP, Lamm W, Clark C, MacFarquhar J, Walton AL, et al. Health care–associated bloodstream infections in adults: a reason to change the accepted definition of community-acquired infections. Ann Intern Med. 2002;137(10):791–7.

    Article  PubMed  Google Scholar 

  19. Darouiche RO. Spinal epidural abscess. N Engl J Med. 2006;355(19):2012–20.

    Article  CAS  PubMed  Google Scholar 

  20. CLSI. Performance standards for antimicrobial susceptibility testing. 2018.

  21. Compain F, Babosan A, Brisse S, Genel N, Audo J, Ailloud F, Kassis-Chikhani N, Arlet G, Decré D. Multiplex PCR for detection of seven virulence factors and K1/K2 capsular serotypes of Klebsiella pneumoniae. J Clin Microbiol. 2014;52(12):4377–80.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Catalán-Nájera JC, Garza-Ramos U, Barrios-Camacho H. Hypervirulence and hypermucoviscosity: Two different but complementary Klebsiella spp. phenotypes? Virulence. 2017;8(7):1111–23.

    Article  PubMed  Google Scholar 

  23. Banerjee T, Wangkheimayum J, Sharma S, Kumar A, Bhattacharjee A. Extensively Drug-Resistant Hypervirulent Klebsiella pneumoniae From a Series of Neonatal Sepsis in a Tertiary Care Hospital, India. Front Med (Lausanne). 2021;8:645955.

    Article  Google Scholar 

  24. Tang M, Kong X, Hao J, Liu J. Epidemiological Characteristics and Formation Mechanisms of Multidrug-Resistant Hypervirulent Klebsiella pneumoniae. Front Microbiol. 2020;11:581543.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Berbari EF, Kanj SS, Kowalski TJ, Darouiche RO, Widmer AF, Schmitt SK, Hendershot EF, Holtom PD, Huddleston PM 3rd, Petermann GW, et al. 2015 Infectious Diseases Society of America (IDSA) Clinical Practice Guidelines for the Diagnosis and Treatment of Native Vertebral Osteomyelitis in Adults. Clin Infect diseases: official publication Infect Dis Soc Am. 2015;61(6):e26–46.

    Article  Google Scholar 

  26. Russo TA, Olson R, MacDonald U, Beanan J, Davidson BA. Aerobactin, but not yersiniabactin, salmochelin, or enterobactin, enables the growth/survival of hypervirulent (hypermucoviscous) Klebsiella pneumoniae ex vivo and in vivo. Infect Immun. 2015;83(8):3325–33.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We thank Mallikarjun Handigund, Ph.D., Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, for his contribution in generating the data for this study.

Funding

This paper was supported by research funds for newly appointed professors of Jeonbuk National University in 2021. And, this paper was supported by Fund of Biomedical Research Institute, Jeonbuk National University Hospital. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Authors and Affiliations

  1. Department of Internal Medicine, Jeonbuk National University Medical School and Hospital, 20 Geonjiro, Deokjin-gu, 54907, Jeonju-si, Jeollabuk-do, South Korea

    Joo-Hee Hwang & Jeong-Hwan Hwang

  2. Research Institute of Clinical Medicine, Biomedical Research Institute of Jeonbuk National University Hospital, 20 Geonjiro, Deokjin-gu, 54907, Jeonju-si, Jeollabuk-do, South Korea

    Joo-Hee Hwang, Seung Yeob Lee, Jaehyeon Lee & Jeong-Hwan Hwang

  3. Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, 20 Geonjiro, Deokjin-gu, 54907, Jeonju-si, Jeollabuk-do, South Korea

    Seung Yeob Lee & Jaehyeon Lee

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Contributions

All authors meet the ICMJE authorship criteria. JeongHH and JHL designed the study, analyzed and interpreted the patient and microbiological data, performed the literature search, and prepared the manuscript. JHL and SYL analyzed and interpreted the microbiological data. JooHH and JeongHH participated in the collection of patient’s data and data interpretation. JooHH and SYL wrote the paper. All authors contributed to the drafting of the manuscript, and read and approved the final version.

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Correspondence to Jaehyeon Lee or Jeong-Hwan Hwang.

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Ethics approval and consent to participate

This study was approved and conducted consistent with the guidelines established by the Institutional Review Board of the Jeonbuk National University Hospital (IRB no.: CUH 2021-11-006). Institutional Review Board of the Jeonbuk National University Hospital waived the need for specific informed consent from study participants because this study data was anonymized, so could not identify the subjects.

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The authors of this study declare no commercial relationships and no conflicts of interest.

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Hwang, JH., Lee, S.Y., Lee, J. et al. Pyogenic spondylitis caused by Klebsiella pneumoniae: should the possibility of hypervirulent Klebsiella pneumoniae be considered?. BMC Infect Dis 22, 801 (2022). https://doi.org/10.1186/s12879-022-07785-6

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BMC Infectious Diseases

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