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Inicio Enfermedades Infecciosas y Microbiología Clínica (English Edition) Streptococcus gallolyticus subsp. gallolyticus knee periprosthetic joint infecti...
Información de la revista
Vol. 40. Núm. 6.
Páginas 337-338 (junio - julio 2022)
Vol. 40. Núm. 6.
Páginas 337-338 (junio - julio 2022)
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Streptococcus gallolyticus subsp. gallolyticus knee periprosthetic joint infection
Infección de prótesis de rodilla por Streptococcus gallolyticus subsp. gallolyticus
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Raquel Fernández-Gonzáleza,
Autor para correspondencia
raquelferngonz@gmail.com

Corresponding author.
, Juan Otero-Villarb, Rodrigo Estévez-Vilarb, María Dolores Díaz-Lópezc
a Servicio de Medicina Interna, Hospital Universitario de Ourense, Ourense, Spain
b Servicio de Traumatología, Hospital Universitario de Ourense, Ourense, Spain
c Unidad de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Ourense, Ourense, Spain
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The Streptococcus bovis/Streptococcus equinus complex (SBSEC), in particular Streptococcus gallolyticus subsp. gallolyticus, has generated interest in recent years in light of the link detected between infections with this micro-organism and colorectal cancer.1 Below we report an uncommon case: a periprosthetic knee infection with S. gallolyticus subsp. gallolyticus.

A 67-year-old patient underwent a total left knee replacement in 2016 due to knee osteoarthritis. In 2019, she sought care for gradually worsening knee pain over the past 12 months with no history of trauma, after having been pain-free for two years following her operation. Initial examination revealed signs of inflammation, with a C-reactive protein (CRP) level of 6.4 mg/dl. Periprosthetic infection was suspected, and therefore diagnostic arthrocentesis was performed. This procedure yielded a cloudy fluid with glucose 142 mg/dl and protein 4.6 g/dl (the bloody and viscous nature of the fluid precluded a cell count). After 48 h, growth of S. gallolyticus subsp. gallolyticus (sensitive to penicillin, cefotaxime and vancomycin and resistant to clindamycin and levofloxacin) was reported. Six months earlier, the patient had undergone a colonoscopy involving polypectomy of a tubulovillous adenoma with low-grade dysplasia.

Surgery was performed in two stages. The first stage included prosthesis removal with debridement, lavage and placement of a BioFix spacer with antibiotics (vancomycin plus gentamicin). After intraoperative samples had been collected, ceftriaxone 2 g/12 h was started. S. gallolyticus subsp. gallolyticus was isolated in these samples and found to have the same antibiogram as in the synovial fluid. The patient followed a favourable course after the operation, completing 14 days of parenteral treatment, followed by oral amoxicillin 1 g/8 h for eight weeks. During admission, she underwent a transthoracic echocardiogram, which yielded no imaging indicative of endocarditis, as well as blood cultures before starting antibiotic therapy, which came back negative, and an abdominal ultrasound, which was normal.

The second stage of the surgery was performed six months later. The patient was given preoperative prophylaxis with ceftriaxone plus teicoplanin, and a total knee replacement was performed. Antibiotic therapy with ceftriaxone was maintained, then discontinued after one week in light of negative results for cultures of intraoperative samples. The patient was followed up on an outpatient basis without incident.

The SBSEC comprises seven species distinguished using molecular biology techniques, with a recent change in taxonomy: S. equinus, S. alactolyticus, S. gallolyticus subsp. gallolyticus (biotype i), S. gallolyticus subsp. macedonicus, S. gallolyticus subsp. pasteurianus (biotype ii/2), S. infantarius subsp. infantarius (biotype ii/1) and S. infantarius subsp. coli (biotype ii/1).2 The usefulness of this distinction lies in the fact that the biotype apparently associated with colon cancer at a higher rate is biotype i (S. gallolyticus subsp. gallolyticus).1

These catalase- and oxidase-negative micro-organisms are Gram-positive cocci and facultative anaerobes that express Lancefield antigen group D in their cell wall. They form part of the intestinal microbiota in 5%–16% of healthy adults. These micro-organisms have been linked to infections in animals and humans. They are causal agents of bacteraemia and endocarditis, as well as meningitis and urinary tract infections, biliary tract infections and osteoarticular infections. Arthritis is less common than spondylodiscitis.3

Periprosthetic knee infection is a serious complication with an incidence of 0.4%–3.9%.4 Risk factors include immunosuppression, diabetes mellitus and malnutrition. The most commonly isolated pathogens are Staphylococcus spp. (both Staphylococcus aureus and coagulase-negative staphylococci);5 cases caused by Streptococcus bovis are rare.

In 2016, García-País et al. published a review of cases of osteoarticular infection due to group B streptococci (GBS) reported to date in which they found 11 cases of periprosthetic joint infection due to GBS.3 In 2020, Mayo Clinic published a review of 2459 cases of periprosthetic joint infection and identified GBS as causal in just nine cases, amounting to 0.4% of the total.6 In most cases, the species could not be identified; S. gallolyticus subsp. gallolyticus was identified in four cases. In the majority of the patients, the antibiotic therapy administered consisted of ceftriaxone 2 g/24 h for four to eight weeks. Among those for whom surgery-related data were available, the average time elapsed between the first and the second stage of surgery was 48 weeks.6

Our case report corresponds to a late periprosthetic knee infection by S. gallolyticus subsp. gallolyticus, a very uncommon pathogen in infections of this nature. It was likely of haematogenous origin, given the patient's history of colonic disease with manipulation prior to the onset of her signs and symptoms, since there appears to be a relationship between abnormalities in the intestinal mucosa and periprosthetic joint infection with S. gallolyticus subsp. gallolyticus. Our patient had a colon tumour as a risk factor when her joint signs and symptoms developed.

Authors

All authors made intellectual contributions to the article and approved the final version thereof.

Conflicts of interest

The authors declare that they have no conflicts of interest.

References
[1]
J. Corredoira Sánchez, F. García Garrote, R. Rabuñal, L. López Roses, M.J. García País, E. Castro, et al.
Association between bacteriemia due to Streptococcus gallolyticus subps. Galloliticus (S. bovis 1) and colorrectal cancer: a case-control study.
Clin Infect Dis, 55 (2012), pp. 491-496
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An Update on the Sreptococcus bovis group: classification, identification, and disease associations.
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Streptococcus bovis septic arthitis and osteomielitis: a report of 21 cases and a literatura review.
Semin Arthitis Rheum, 45 (2016), pp. 738-746
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J.E. Phillips, T.P. Crane, M. Noy, T.S. Elliot, R.J. Grimer.
The incidence of deep prosthetic infections in a specialist orthopaedic hospital: a 15-year prospective survey.
J Bone Joint Surg Br, 88 (2006), pp. 943-948
[5]
A. Stefansdottir, D. Johansson, K. Knutson, L. Lidgren, O. Robertsson.
Microbiology of the infected knee arthroplasty: report from Swedish Knee Artroplasty Registe ron 426 surgically revised cases.
Scand J Infect Dis, 41 (2009), pp. 831-840
[6]
J.C. Thompson, A.H. Goldman, A.J. Tande, D.R. Osmon, R.J. Sierra.
Streptococcus bovis hip and knee periprosthetic joint infections: a series of 9 cases.
J. Bone Joint Infect, 5 (2020), pp. 1-6

Please cite this article as: Fernández-González R, Otero-Villar J, Estévez-Vilar R, Díaz-López MD. Infección de prótesis de rodilla por Streptococcus gallolyticus subsp. gallolyticus. Enferm Infecc Microbiol Clin. 2022;40:337–338.

Copyright © 2021. Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
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