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  • Case report
  • Open Access
  • Open Peer Review

Bilateral osteomyelitis and liver abscess caused by hypervirulent Klebsiella pneumoniae- a rare clinical manifestation (case report)

BMC Infectious Diseases201818:380

https://doi.org/10.1186/s12879-018-3277-4

  • Received: 26 October 2017
  • Accepted: 27 July 2018
  • Published:
Open Peer Review reports

Abstract

Background

Hypervirulent strains of Klebsiella pneumoniae are a recognized cause of a distinct invasive syndrome that results in pyogenic liver abscesses and metastatic complications, particularly in the Asia Pacific region. Reports of hypervirulent K.pneumoniae in Europe, the Americas and Australia indicate worldwide spread. We present a case of multi-focal osteomyelitis, a rarely described complication of hypervirulent K.pneumoniae in the medical literature. The prevalence of this condition in countries outside Asia may be expected to rise with increasing travel.

Case presentation

A 20-year-old Chinese man residing in Australia for 2 years presented with a 2-week history of gradually worsening leg pain preceded by 2 weeks of constitutional symptoms. Imaging with computerized axial tomography (CT) and other modalities revealed bilateral tibial lesions described as lattice-like linear lucencies involving the cortices with scalloping of the outer involved cortex. Cultures of tissue from a left tibial bone biopsy were positive cultures for K.pneumoniae. Whole-genome sequencing identified the isolate as K1 serotype ST23, a well-recognized hyper virulent strain capable of causing invasive disease. An abdominal CT revealed a 27x22mm liver abscess. The patient had no other metastatic manifestations of the disease, and responded to 6 weeks of intravenous ceftriaxone followed by 3 months of oral Ciprofloxacin.

Conclusions

Increased awareness of the manifestations and subsequent management of hyper virulent strains of K.pneumoniae by clinicians is important to assist early recognition and help minimize serious sequelae. Cases with overseas links, such as previous residence in the Asia Pacific area, are at higher risk for infection with the hyper virulent strain. This case highlights the need for clinicians to be able to recognize this important disease, especially in patients with the right epidemiological links, and to investigate and treat appropriately to prevent severe metastatic complications.

Keywords

  • Klebsiella pneumoniae
  • Hypervirulent
  • Osteomyelitis
  • Pyogenic liver abscess

Background

Klebsiella pneumoniae is a common pathogen responsible for infections such as urinary tract infections, community acquired pneumonia or surgical site infections. Hyper virulent strains are a distinct population of K.pneumoniae, causing the well-recognized “invasive syndrome” that results in pyogenic liver abscesses, as well as extrahepatic metastatic infectious manifestations resulting from bacteraemic dissemination [1]. Rarer complications include necrotizing fasciitis, osteomyelitis, prostatic abscesses and meningitis [2].

Bilateral pyogenic osteomyelitis as a clinical entity is exceedingly rare [38] as is long bone osteomyelitis attributable to infection with hyper virulent K.pneumoniae [9]. We describe a rare case of bilateral tibial osteomyelitis and liver abscess resulting from infection with hypervirulent K.pneumoniae in a previously healthy Chinese student at our Australian health service.

Case presentation

A previously well twenty-four-year-old student from Hong Kong was referred to our health service with a 2-week history of gradually worsening leg pain and plain film X-ray changes suggestive of an uncharacterized bilateral bony destructive process. The pain was preceded by a 2-week history of constitutional symptoms, including night sweats, chills, fevers, headache, malaise, and a mildly productive cough, which resolved with the onset of bilateral lower limb pain.

There was no past history of Tuberculosis exposure or infection, and routine vaccinations were up to date. The patient reported no overseas travel since his arrival in Australia two years’ prior, denied recreational drug use, and was a non-smoker and drinker. He had no recent animal contacts.

Prior to presentation, a course of oral cephalexin was prescribed for presumed cellulitis, which made no difference to his systemic symptoms. On presentation, there was focal pain over the left and right anterior tibial surface. On examination, there was no clinical evidence of a subcutaneous collection. Further imaging of his lower limbs with a computerized axial tomography (CT) scan of both legs revealed bilateral tibial lesions with pronounced changes on the right, described as lattice-like linear lucencies involving the cortices with scalloping of the outer involved cortex. There was no soft tissue mass or periosteal reaction. These changes were further confirmed by a magnetic resonance imaging (MRI) and Technetium-99 m bone scan (Fig. 1). An initially elevated white cell count of 12.2 × 109/L normalized after admission. He had a persistently raised C-reactive protein (CRP), which peaked at 130 mg/L, and an erythrocyte sedimentation rate (ESR) of 88 mm/h. Liver function testing, initially normal, became deranged with a cholestatic picture on day 12 of his admission. A human immunodeficiency virus (HIV) screen and vasculitis screen were negative. Multiple serial blood cultures were negative.
Fig. 1
Fig. 1

Technetium-99 m bone scan, showing markedly increased tracer uptake of the left tibial and distal fibular shaft, and mid to distal right tibial shaft

Further investigation with a left tibial bone biopsy was performed, with positive cultures for K.pneumoniae on the fresh tissue specimen. The organism was identified using matrix assisted laser desorption ionization-time of flight mass spectrometry ((MALDI-TOF MS, BrukerDaltonics, Biotyper 3.0 database). Antibiotic susceptibility profile was determined using direct colony suspension of 0.5 McFarland on Mueller-Hinton agar. Minimum inhibitory concentration values were interpreted in accordance with Clinical & Laboratory Standards Institute (CLSI) guidelines. The isolate was phenotypically resistant to ampicillin but sensitive to cefazolin, sulphamethoxazole/trimethoprim, gentamicin and ciprofloxacin.

Whole-genome sequencing of the isolate was performed on the Illumina NextSeq using manufacturer protocols (Illumina Inc., San Diego, CA, USA) [10]. In silico multi-locus sequence typing and analysis of the capsular polysaccharide locus identified the isolate as a K1 serotype, sequence type 23 (ST23) K. pneumoniae, a well-recognized hyper virulent strain capable of causing invasive disease. It also possessed a hypermucoid phenotype demonstrated by string test positivity (Fig. 2). Several other virulence genes and operons were also detected, including the mucoviscosity genes magA, rmpA and rmpA2, the allantoin anaerobic assimilation operon allABCDRS, the ferric uptake system kfuABC, and the yersiniabactin, aerobactin (including the iutA gene), siderobactin and colibactin siderophore systems. The only antibiotic resistance elements detected were blaSHV-36 and fosA.
Fig. 2
Fig. 2

Culture of the isolate from the bone biopsy demonstrating hypermucosity, as evidenced by the formation of a string greater than 5 mm in length using a standard inoculation loop

Subsequent CT of the abdomen performed to investigate for a gastrointestinal source of his infection revealed a 27x22mm lesion in segment 8 of the liver, consistent with liver abscess and confirmed on ultrasound, which was not amenable to surgical drainage. On inpatient Ophthalmology review the patient had no signs of endophthalmitis. He was commenced on a 6-week course of intravenous (IV) ceftriaxone at 2 g daily.

Subsequently, his pain markedly improved. Treatment was well tolerated and after 6 weeks of therapy inflammatory markers had normalised, with only minor persistent pain and erythema in the left leg. He then completed a 3-month course of oral Ciprofloxacin with no further evidence of disease relapse. After 3 months the patient was lost to follow up, precluding repeat imaging to assess for resolution of his liver abscess.

Discussion

The first described case series of K.pneumoniae pyogenic liver abscess with metastatic characteristics in the form of endophthalmitis was from Taiwan in the 1980s [11]. The organism has since been recognized as causing a severe metastatic syndrome in previously healthy hosts, particularly in the Asian Pacific region. The organism is now the main cause of liver abscesses in Singapore, Hong Kong, South Korea and Taiwan [12]. Increasing global travel has resulted in reported cases from Europe, the Americas [9] and Australia [13, 14], indicating worldwide spread of the disease.

Hypervirulent strains of K.pneumoniae have traditionally been susceptible to most antibiotics compared with the carbapenem resistant strains that have caused large outbreaks in the nosocomial setting [1517]. However, a variety of resistance mechanisms, including proposed transmission of mobile genetic elements between “classic” and hypervirulent strains of K.pneumoniae [18], have resulted in outbreaks of carbapenem-resistant hypervirulent strains in China [18, 19] and other parts of the world [18]. These strains pose a substantial threat to human health because they have potential to cause invasive and severe disease, are highly transmissible and are extremely difficult to treat.

A combination of specific microbiological and host attributes may contribute to disease development. Proposed diagnostic clinical criteria for the invasive syndrome of K.pneumoniae include probable invasive nature, with isolated liver abscess, or definite invasive, which comprises extra-hepatic manifestations [12]. Microbiological definitions of probable and definite invasive disease include string test positivity, and identification of K1 or K2 serotypes, respectively.

The isolate from this case was of capsular serotype K1, a sequence type 23 strain, with confirmed presence of the wzy-K1 gene (previously magA), now known to encode serotype K1 capsule formation [20]. ST23 is the strain most frequently isolated from invasive infections [21]. The emergence of virulence in these isolates of the same lineage have occurred with the presence of siderophores, demonstrating that the acquisition of iron scavenging systems are crucial in the ability of K.pneumoniae to cause invasive disease [21]. The presence of the ‘mucoid regulator genes’, rmpA and rmpA2, which can upregulate capsule production has also been associated with hypervirulence and, phenotypically, string test positivity [22].

The Chinese ethnicity of our patient has also been demonstrated to be a risk factor for invasive disease [23]. Studies have linked carriage of virulent strains of K. pneumoniae in the gastrointestinal tract of healthy hosts as a predisposing factor for development of pyogenic liver abscesses in patients of Asian descent [24, 25]. Although faecal analysis was not completed on our patient, this may have been a predisposing factor in our patient.

A combination of these genes in the ST23 strains and factors related to ethnicity have likely resulted in the emergence of the hypervirulent phenotype in our case, with evidence of pyogenic liver abscess and multi-focal osteomyelitis.

Though well described in children, acute osteomyelitis caused by haematogenous spread is uncommon in adults with no underlying co-morbidities [26, 27]. Acute bilateral long bone osteomyelitis from a pyogenic cause is rarely encountered in clinical practice. Although an established complication of invasive disease, there are limited published cases of primary osteomyelitis caused by invasive K.pneumoniae [9]. The possibility of multifocal osteomyelitis was initially raised in this case based on the clinical history of preceding constitutional symptoms and the imaging findings. A malignant process such as osteosarcoma was deemed less likely given the absence of aggressive periosteal reaction or expansive medullary cavity mass on imaging. Given its atypical presentation, this case presented an initial diagnostic challenge requiring careful clinical and radiographic correlation, as well as consideration of the relevant epidemiological background.

Conclusions

In an increasingly globalised world, our study highlights the importance of clinician awareness of the manifestations and management of K.pneumoniae hypervirulent strains, even in areas with few described cases. Further testing and prompt evaluation for the hyper virulent strain in the right clinical context is important to reduce the morbidity and mortality. This is even more crucial with the emergence of carbapenem resistant strains of hyper virulent K.pneumoniae. Multi-focal osteomyelitis caused by K. pneumoniae is rarely described in the literature. Our case contributes to the growing awareness of the unusual manifestations of this serious disease.

Abbreviations

CLSI: 

Clinical & Laboratory Standards Institute

CRP: 

C-reactive protein

CT: 

Computerized Axial Tomography

ESR: 

Erythrocyte Sedimentation Rate

HIV: 

Human Immunodeficiency Virus

IV: 

Intravenous

K. pneumoniae

Klebsiella pneumoniae

MRI: 

Magnetic Resonance Imaging

ST23: 

Sequence Type 23

Declarations

Funding

This project was funded by the Barwon Health Department of Infectious Diseases research fund. The funding was utilized during analysis and interpretation of the data, specifically in performing whole-genome sequencing on the K.Pneumoniae isolate. During the write-up of the manuscript, the funding also assisted with administrative fees involved in the publication process.

Availability of data and materials

All data generated or analyzed during this study during whole genome sequencing of the bacterial isolate are included in this published article and its supplementary information files.

Authors’ contributions

BL, JK and BH were involved in microbiological analysis of the initial isolate, antibiotic susceptibility analysis and subsequent genome sequencing of the bacterial strain. RDA and RA were members of the primary treating team and performed the diagnostic biopsy and intra-operative assessment. JP, EA, AT and ES were members of the treating consultative team and were major contributors in writing the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The subject of this case report provided full written consent to participate.

Consent for publication

The subject of this case report provided full written consent to the publication of case-relevant information pertaining to his medical history and any radiographic images submitted.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Department of Infectious Diseases, Barwon Health, Bellarine Street, Geelong, VIC, 3220, Australia
(2)
Doherty Applied Microbial Genomics and Microbiological Diagnostic Unit Public Health Laboratory, University of Melbourne at The Peter Doherty Institute for Infection & Immunity, Melbourne, Victoria, 3000, Australia
(3)
School of Medicine, Deakin University, Geelong, Australia
(4)
Department of Orthopaedics, Barwon Health, Bellarine Street, Geelong, VIC, 3220, Australia

References

  1. Yu VL, Hansen DS, Ko WC, Sagnimeni A, Klugman KP, Von Gottberg A, et al. Virulence characteristics of Klebsiella and clinical manifestations of K. pneumoniae bloodstream infections. Emerg Infect Dis. 2007;13(7):986–93.View ArticlePubMedPubMed CentralGoogle Scholar
  2. Shon AS, Bajwa RP, Russo TA. Hypervirulent (hypermucoviscous) Klebsiella pneumoniae: a new and dangerous breed. Virulence. 2013;4(2):107–18.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Sipahioglu S, Askar H, Zehir S. Bilateral acute tibial osteomyelitis in a patient without an underlying disease: a case report. J Med Case Rep. 2014;8:388.View ArticlePubMedPubMed CentralGoogle Scholar
  4. Crook E. Bilateral osteomyelitis of tibia. Proc R Soc Med. 1929;22(7):899–900.PubMedPubMed CentralGoogle Scholar
  5. Billups KL, Stultz JS. Successful Daptomycin use in a pediatric patient with acute, bilateral osteomyelitis caused by methicillin-resistant Staphylococcus aureus. J Pediatr Pharmacol Ther. 2015;20(5):397–402.PubMedPubMed CentralGoogle Scholar
  6. Bachmeyer C, Entressengle H, Gibeault M, Nédellec G, M'Bappé P, Delisle F, et al. Bilateral tibial chronic osteomyelitis due to Pantoea agglomerans in a patient with sickle cell disease. Rheumatology (Oxford). 2007;46(8):1247.View ArticleGoogle Scholar
  7. Javaloyas M, Sanchez C, Garau J, Valverde J. Bilateral and symmetrical osteomyelitis due to gram-negative bacilli. A report on two cases. Scand J Rheumatol. 1985;14(3):289–92.View ArticlePubMedGoogle Scholar
  8. Picillo U, Italian G, Marcialis MR, Ginolfi F, Abbate G, Tufano MA. Bilateral femoral osteomyelitis with knee arthritis due to Salmonella enteritidis in a patient with systemic lupus erythematosus. Clin Rheumatol. 2001;20(1):53–6.View ArticlePubMedGoogle Scholar
  9. Prokesch BC, TeKippe M, Kim J, Raj P, TeKippe EM, Greenberg DE. Primary osteomyelitis caused by hypervirulent Klebsiella pneumoniae. Lancet Infect Dis. 2016;16(9):e190–5. https://doi.org/10.1016/S1473-3099(16)30021-4.View ArticlePubMedGoogle Scholar
  10. Fookes M, Yu J, De Majumdar S, Thomson N, Schneiders T. Genome sequence of Klebsiella pneumoniae Ecl8, a reference strain for targeted genetic manipulation. Genome Announc. 2013;1(1) https://doi.org/10.1128/genomeA.00027-12.
  11. Liu YC, Cheng DL, Lin CL. Klebsiella pneumoniae liver abscess associated with septic endophthalmitis. Arch Intern Med. 1986;146(10):1913–6.View ArticlePubMedGoogle Scholar
  12. Siu LK, Yeh KM, Lin JC, Fung CP, Chang FY. Klebsiella pneumoniae liver abscess: a new invasive syndrome. Lancet Infect Dis. 2012;12(11):881–7.View ArticlePubMedGoogle Scholar
  13. Anstey JR, Fazio TN, Gordon DL, Hogg G, Jenney AW, Maiwald M, et al. Community-acquired Klebsiella pneumoniae liver abscesses - an "emerging disease" in Australia. Med J Aust. 2010;193(9):543–5.PubMedGoogle Scholar
  14. Dulku G, Tibballs J. Cryptogenic invasive Klebsiella pneumoniae liver abscess syndrome (CIKPLA) in Western Australia? Australas Med J. 2014;7(11):436–40.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Pitout JD, Nordmann P, Poirel L. Carbapenemase-producing Klebsiella pneumoniae, a key pathogen set for global nosocomial dominance. Antimicrob Agents Chemother. 2015;59(10):5873–84.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Parisi SG, Bartolini A, Santacatterina E, Castellani E, Ghirardo R, Berto A, et al. Prevalence of Klebsiella pneumoniae strains producing carbapenemases and increase of resistance to colistin in an Italian teaching hospital from January 2012 to December 2014. BMC Infect Dis. 2015;15:244.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Tada T, Tsuchiya M, Shimada K, Nga TTT, Thu LTA, Phu TT, et al. Dissemination of Carbapenem-resistant Klebsiella pneumoniae clinical isolates with various combinations of Carbapenemases (KPC-2, NDM-1, NDM-4, and OXA-48) and 16S rRNA Methylases (RmtB and RmtC) in Vietnam. BMC Infect Dis. 2017;17:467.View ArticlePubMedPubMed CentralGoogle Scholar
  18. 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.View ArticlePubMedPubMed CentralGoogle Scholar
  19. 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. 2017;18(1):37–46. https://doi.org/10.1016/S1473-3099(17)30489-9.View ArticlePubMedGoogle Scholar
  20. Fang CT, Lai SY, Yi WC, Hsueh PR, Liu KL. The function of wzy_K1 (magA), the serotype K1 polymerase gene in Klebsiella pneumoniae cps gene cluster. J Infect Dis. 2010;201:1268–9.View ArticlePubMedGoogle Scholar
  21. 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 U S A. 2015;112(27):E3574–81. https://doi.org/10.1073/pnas.1501049112.View ArticlePubMedPubMed CentralGoogle Scholar
  22. Cheng HY, Chen YS, Wu CY, Chang HY, Lai YC, Peng HL. RmpA regulation of capsular polysaccharide biosynthesis in Klebsiella pneumoniae CG43. J Bacteriol. 2010;192(12):3144–58.View ArticlePubMedPubMed CentralGoogle Scholar
  23. Lee IR, Molton JS, Wyres KL, Gorrie C, Wong J, Hoh CH, et al. Differential host susceptibility and bacterial virulence factors driving Klebsiella liver abscess in an ethnically diverse population. Sci Rep. 2016;6:29316.View ArticlePubMedPubMed CentralGoogle Scholar
  24. Chung DR, Lee H, Park MH, Jung SI, Chang HH, Kim YS. Fecal carriage of serotype K1 Klebsiella pneumoniae ST23 strains closely related to liver abscess isolates in Koreans living in Korea. Eur J Clin Microbiol Infect Dis. 2012;31(4):481–6.View ArticlePubMedGoogle Scholar
  25. Lin YT, Siu LK, Lin JC, Chen TL, Tseng CP, Yeh KM, et al. Seroepidemiodatalogy of Klebsiella pneumoniae colonizing the intestinal tract of healthy Chinese and overseas Chinese adults in Asian countries. BMC Microbiol. 2012;12(13):1–7.Google Scholar
  26. Dirschl DR1 AL. Osteomyelitis. Common causes and treatment recommendations. Drugs. 1993;45(1):29–43.View ArticleGoogle Scholar
  27. Lew DP, Waldvogel FA. Osteomyelitis. Lancet. 2004;364:369–79.View ArticlePubMedGoogle Scholar

Copyright

© The Author(s). 2018

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