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Spondylodiscitis in a healthy 12-year-old girl with Extraintestinal pathogenic Escherichia coli (ExPEC) bacteraemia
BMC Infectious Diseasesvolume 17, Article number: 380 (2017)
Escherichia coli (E. coli) is rarely implicated in bone or joint infections in children.
We discuss the case of a healthy 12-year-old girl with an E. coli bacteraemia and a T11-T12 spondylodiscitis revealed by magnetic resonance imaging. The strain harboured serogroup O1:K1 and virulence factors common to highly virulent extra intestinal pathogenic E. coli (ExPEC). Immunological work-up was normal.
The identification of E. coli in a spondylodiscitis should lead to the search for immunosuppression of the host and virulence factors of the strain, particularly those of ExPEC.
Bone and joint infections are common in children, and spine is affected in 1–4% of cases . Native vertebral osteomyelitis is often the result of hematogenous seeding of the adjacent disc space from a distant focus, as the disc is avascular. Pyogenic spondylodiscitis usually occur in young children, and the main pathogen is Staphylococcus aureus ; Gram-negative bacteria are rarely implicated in children as in adults. Among Gram-negative bacteria, E. coli is the most frequent in spondylodiscitis in adults ; the main risk factors are a pre-existing or synchronous genitourinary tract infection or an intra-abdominal infection [3, 4].
A 12-year-old caucasian girl presented with a 1-day history of fever (39 °C) with right lumbar pain. She had no medical history and had never travelled outside Western Europe. There was no report of dysuria, frequent daytime urination, abdominal pain or diarrhoea. Physical examination was normal apart from a right lumbar punch. White blood cell (WBC) count was 9400/mm3, neutrophils 7600/mm3 and CRP 16 mg/L. Blood and urines were collected for culture and ceftriaxone was started for suspicion of pyelonephritis. Urinalysis was negative for leukocyte, nitrite and pyuria. Urinary culture was sterile but one blood culture was positive for an Escherichia coli strain susceptible to all antibiotics. Abdominal ultrasound and abdominal tomodensitometry with intravenous injection of an iodised contrast product were normal. The patient was afebrile after 48 h of ceftriaxone. C-Reactive Protein (CRP) culminated at 78 mg/L on day 2 and lowered at 12 mg/L on day 5.
However, lumbar pain persisted despite paracetamol and required morphine. A second renal ultrasound was performed and showed no sign of urinary lithiasis. A magnetic resonance imaging of the spine on day 7 revealed a T11-T12 spondylodiscitis without adjacent epidural or soft tissue inflammation (Fig. 1). No bone biopsy was attempted. It would have been considered if the clinical evolution had been unfavourable despite antibiotic treatment. A corset was prescribed and ciprofloxacin was added on day 6 to complete a 14-day course of intravenous antibiotherapy. She had minimal back pain on day 14 and was discharged with oral ciprofloxacin for another 4 weeks. She complained of arthralgia of both wrists on day 35. Physical examination was normal. Ciprofloxacin was stopped on day 42 and arthralgia resolved spontaneously.
Polymerase chain reactions (PCR) were performed to analyze E. coli strain, as described previously [5,6,7]. It harbored serogroup O1:K1 and belonged to the major phylogenetic group B21. Among 23 genetic determinants encoding virulence factors (VFs) investigated [5,6,7]. 14 were present, including genes coding for siderophores (yersiniabactin - fyuA, aerobactin - iucC, sit system - sitA, salmochelin – iroN), adhesins P fimbriae (papGII but not papGIII), pilin (papC), vacuolating toxin (vat) and cytolethal distending toxin (cdt). Moreover, strain had other genetic determinants: colicin V (cvaA), colicin Ia (cia), a pore-forming toxin gene that increases serum survival (iss), a type I secretion system operon (ets), a putative outer membrane protease (ompT) and a hemolysin (hlyF) which combined with the aerobactin and salmochelin genes are characteristic of a conserved virulence plasmidic region identified in the highly virulent extra intestinal pathogenic E. coli strain S88 . Finally, PCR were negative for other adhesin/invasin genes (sfa/foc and ibeA), alpha-hemolysin (hlyA), cytotoxic necrotizing factor (nf1), secreted autotransporter toxin (sat) and colibactin (clbB).
Immunological explorations including WBC count and smear, the determination of plasma IgA, G, M and E and IgG subclasses levels and classic complement pathway analysis were normal. The absence of previous unusual infection in our patient didn’t lead us further explores her immunity to rule out an immunodeficiency.
Here, our patient had no diarrhoea, and urine culture and imaging ruled out a genitourinary tract or intestinal infection. There was no history of trauma or injury associated with the spine. We speculated the spine was involved because of the good vascularisation of the disk in children. Moreover, she had no underlying condition and immunological work-up didn’t favour a primary immunodeficiency. The characterization of the strain of E. coli involved in our case, particularly its virulence factors, was therefore instructive.
Extraintestinal pathogenic Escherichia coli (ExPEC) bloodstream infections represent a growing public health concern [8, 9]. ExPEC strains have acquired genes encoding virulence factors that allow them to cause infections outside the gastrointestinal tract. The B2 phylogenetic group is the main one implicated in various extra intestinal infections  and in 63% of E. coli bacteraemia in French children . This proportion is similar whether the identified portal of entry is the urinary tract or the digestive tract. The most frequent extra-intestinal virulence genes identified in this nation-wide study were fyuA, irp2, iraT, ompT, iucC, iron, papC and papGII. Our strain belonged to the B21 subgroup, one of the most virulent subgroup, and harbored 6 of these 8 virulence factors, namely fyuA, ompT, iucC, iron, papC and papGII: those could explain the predisposition of this strain to be bacteraemic. Virulence factors of our strain included adhesins (e.g. P fimbriae), factors to avoid or subvert host defense systems (e.g. capsule K1) and nutrient acquisition factors (e.g. siderophores). However, to our knowledge, no publication has established a link between some virulence factors and bone/joint infections.
Recently, Lemaitre et al. and others showed that the conserved virulence plasmidic region identified in our strain contributed to the high level of bacteremia in neonates [6,7,8,9,10,11,12]. The serotype O1:K1 could also contribute to the virulence of our strain. Beside K1 capsule antigen that provides a survival advantage in serum , O1-antigen serotype might also confer protection against complement killing . However, our strain didn’t have genes hlyA (alpha-hemolysin) nor cnf1 (cytotoxic necrotic factor), two virulence factors identified as highly cytotoxic toward human osteoblastic cells in vitro .
Concerning the antibiotic management of our patient, the French Society for Infectious Diseases recommends intravenous association of a 3rd generation cephalosporin and a fluoroquinolon to treat spondylodiscitis caused by E. coli. The duration of IV therapy or combination therapy is not precised in the recommendations. Given the good clinical evolution and the excellent oral biodisponibility of ciprofloxacin, intravenous and association were stopped on day 14 for oral ciprofloxacin alone.
Escherichia coli is an uncommon cause of spondylodiscitis, particularly in children. The strain harbored serogroup O1:K1 and virulence factors common to highly virulent extra intestinal pathogenic E. coli that could explain this rare clinical presentation. The identification of E. coli in a spondylodiscitis should lead to the search for immunosuppression of the host and virulence factors of the strain, particularly those of ExPEC.
- E. coli :
Extra intestinal pathogenic Escherichia coli
Polymerase chain reaction
White blood cells
Peltola H, Pääkkönen M. Acute osteomyelitis in children. N Engl J med. 2014;370:352–60.
Tyagi R. Spinal infections in children: a review. J Orthop. 2016;13:254–8.
Mylona E, Samarkos M, Kakalou E, Fanourgiakis P, Skoutelis A. Pyogenic vertebral osteomyelitis: a systematic review of clinical characteristics. Semin Arthritis Rheum. 2009;39:10–7.
Kang S-J, Jang H-C, Jung S-I, Choe PG, Park WB, Kim C-J, et al. Clinical characteristics and risk factors of pyogenic spondylitis caused by gram-negative bacteria. PLoS One. 2015;10:e0127126.
Bidet P, Mahjoub-Messai F, Blanco J, Blanco J, Dehem M, Aujard Y, et al. Combined multilocus sequence typing and O serogrouping distinguishes Escherichia coli subtypes associated with infant urosepsis and/or meningitis. J Infect dis. 2007;196:297–303.
Peigne C, Bidet P, Mahjoub-Messai F, Plainvert C, Barbe V, Médigue C, et al. The plasmid of Escherichia coli strain S88 (O45:K1:H7) that causes neonatal meningitis is closely related to avian pathogenic E. coli plasmids and is associated with high-level bacteremia in a neonatal rat meningitis model. Infect Immun. 2009;77:2272–84.
Johnson JR, Johnston B, Kuskowski MA, Nougayrede J-P, Oswald E. Molecular epidemiology and phylogenetic distribution of the Escherichia coli pks genomic island. J Clin Microbiol. 2008;46:3906–11.
Russo TA, Johnson JR. Medical and economic impact of extraintestinal infections due to Escherichia coli: focus on an increasingly important endemic problem. Microbes Infect Inst Pasteur. 2003;5:449–56.
de Kraker MEA, Jarlier V, Monen JCM, Heuer OE, van de Sande N, Grundmann H. The changing epidemiology of bacteraemias in Europe: trends from the European antimicrobial resistance surveillance system. Clin Microbiol Infect Off Publ Eur Soc Clin Microbiol Infect dis. 2013;19:860–8.
Picard B, Garcia JS, Gouriou S, Duriez P, Brahimi N, Bingen E, et al. The link between phylogeny and virulence in Escherichia coli extraintestinal infection. Infect Immun. 1999;67:546–53.
Burdet C, Clermont O, Bonacorsi S, Laouénan C, Bingen E, Aujard Y, Mentré F, Lefort A, Denamur E, COLIBAFI Group. Escherichia coli Bacteremia in children: age and portal of entry are the main predictors of severity. Pediatr Infect dis J. 2014;33:872–9.
Lemaître C, Mahjoub-Messai F, Dupont D, Caro V, Diancourt L, Bingen E, et al. A conserved virulence plasmidic region contributes to the virulence of the multiresistant Escherichia coli meningitis strain S286 belonging to phylogenetic group C. PLoS One. 2013;8:e74423.
Leying H, Suerbaum S, Kroll HP, Stahl D, Opferkuch W. The capsular polysaccharide is a major determinant of serum resistance in K-1-positive blood culture isolates of Escherichia coli. Infect Immun. 1990;58:222–7.
Sarkar S, Ulett GC, Totsika M, Phan M-D, Schembri MA. Role of capsule and O antigen in the virulence of uropathogenic Escherichia coli. PLoS One. 2014;9:e94786.
Crémet L, Broquet A, Brulin B, Jacqueline C, Dauvergne S, Brion R, Asehnoune K, Corvec S, Heymann D, Caroff N. 2015. Pathogenic potential of Escherichia coli clinical strains from orthopedic implant infections towards human osteoblastic cells. Pathog dis 73:ftv065.
Dr. S. Lamer (Service de radiologie, CH Courbevoie-Neuilly).
On the service budget without other funding.
Availability of data and materials
All results and materials and methods are available upon request from the author.
JG, CM and NB were in charge of the patient. MA analyzed the Magnetic Resonance Imaging. JG, GG and SB contributed to the writing of the manuscript. CM and ML revised the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written consent of parents was collected and approved for publication of the case, and the accompanying images, was obtained from the parents.
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Consent was collected and ethic approved.