A clinical case of posttraumatic osteomyelitis associated with kytococcus schroeteri and enterococcus faecalis
- Authors: Borisov S.D.1, Karimov I.F.1, Plotnikov A.O.1,2, Inchagova K.S.2, Pankov A.S.1, Danshin D.P.3
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Affiliations:
- Orenburg State Medical University of the Ministry of Health of Russia
- Institute for Cellular and Intracellular Symbiosis of the Ural Branch of the Russian Academy of Sciences, Orenburg Federal Research Center of the UrB RAS
- Orenburg Regional Clinical Specialized Center of Traumatology and Orthopedics
- Issue: Vol 13, No 5 (2023)
- Pages: 985-994
- Section: FOR THE PRACTICAL PHYSICIANS
- URL: https://journal-vniispk.ru/2220-7619/article/view/158902
- DOI: https://doi.org/10.15789/2220-7619-ACC-15623
- ID: 158902
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Abstract
Introduction. In most cases, osteomyelitis is the monomicrobial disease caused by various Gram-positive bacteria. However, previous injury may contribute to formation of a microbial association. Presence of two or more pathogens in the infectious focus can markedly complicate the disease clinical picture. Kytococcus schroeteri is one of the rarest pathogens found in clinical samples. Slightly more than twenty described cases related to such infection have been recorded globally. The aim of the research was to analyse the first identified clinical case of post-traumatic osteomyelitis associated with Kytococcus schroeteri and Enterococcus faecalis. Materials and methods. The bacterial cultures were obtained from the wound discharge of the patient’s shin by the cultural method. Identification of the bacterial cultures was performed using a VITEK MS mass spectrometer followed by 16S rRNA gene sequencing. The morphological, tinctorial and biochemical features of the cultures obtained were established, and their antibacterial resistance was also determined. Results. The clinical case was associated with the diagnosis “Chronic post-traumatic osteomyelitis of the left shin”. Two types of microorganisms were isolated from the wound discharge, and identified as Kytococcus schroeteri and Enterococcus faecalis using the MALDI-ToF mass spectrometry method. 16S rRNA gene sequencing from the isolated bacterial cultures confirmed the MALDI-ToF mass spectrometry data. Antimicrobial susceptibility for this microorganism was determined according to the criteria for the staphylococcal group according to the clinical guide “Determination of sensitivity to antimicrobial drugs (rev. 2021)”. Conclusion. For the first time, the mixed infection caused by two Gram-positive bacteria K. schroeteri and E. faecalis has been described. Such associations can enhance the pathogenic effects of each other bacterium, which may contribute to transition of the infection to a chronic form with a low probability of positive cultural test. K. schroeteri is a representative of the normal skin microbiota, but this microorganism is able to cause various infections. The K. schroeteri species should be differentiated from other representatives of the order Micrococcales. At cultural examination, resistance to oxacillin is a suspicious sign indicating that the bacterial culture might be potentially assigned to K. schroeteri species. Due to the unavailability of current biochemical tests for differentiation K. schroeteri from related taxa, reliable identification of this species is recommended using MALDI-ToF mass spectrometry or 16S rRNA gene sequencing.
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##article.viewOnOriginalSite##About the authors
Sergey D. Borisov
Orenburg State Medical University of the Ministry of Health of Russia
Email: sdborisov56@mail.ru
PhD (Medicine), Honored Worker of Science of the Russian Federation, Head and Bacteriologist of the Microbiological Laboratory, Science Research Center
Russian Federation, OrenburgIlshat F. Karimov
Orenburg State Medical University of the Ministry of Health of Russia
Email: ifkarimov@yandex.ru
PhD (Biology), Associate Professor of the Department of Microbiology, Virology, Immunology; Biologist of the Microbiological Laboratory, Science Research Center
Russian Federation, OrenburgAndrey O. Plotnikov
Orenburg State Medical University of the Ministry of Health of Russia; Institute for Cellular and Intracellular Symbiosis of the Ural Branch of the Russian Academy of Sciences, Orenburg Federal Research Center of the UrB RAS
Author for correspondence.
Email: protoz@mail.ru
ORCID iD: 0000-0001-6830-4068
SPIN-code: 9543-0734
Scopus Author ID: 7101750076
ResearcherId: C-2198-2013
https://ikvs.info/institut/staff/plotnikov-andrej-olegovich/
PhD (Medicine), Associate Professor, Director, Institute for Cellular and Intracellular Symbiosis; Associate Professor, Department of Preventive Medicine
Russian Federation, Orenburg; OrenburgKsenia S. Inchagova
Institute for Cellular and Intracellular Symbiosis of the Ural Branch of the Russian Academy of Sciences, Orenburg Federal Research Center of the UrB RAS
Email: ksenia.inchagova@mail.ru
PhD (Biology), Senior Researcher, Science Resource Center “Persistence of microorganisms”
Russian Federation, OrenburgAlexandr S. Pankov
Orenburg State Medical University of the Ministry of Health of Russia
Email: nic@orgma.ru
DSc (Medicine), Associate Professor, Head of the Department of Epidemiology and Infectious Diseases, Director of the Science Research Center
Russian Federation, OrenburgDmitry P. Danshin
Orenburg Regional Clinical Specialized Center of Traumatology and Orthopedics
Email: sdborisov56@mail.ru
Traumatologist
Russian Federation, OrenburgReferences
- Техника сбора и транспортирования биоматериалов в микробиологические лаборатории: Методические указания (МУ 4.2.2039-05). М.: Федеральный центр гигиены и эпидемиологии Роспотребнадзора, 2006. 126 с. [Technique for collecting and transporting biomaterials to microbiological laboratories: Guidelines (MU 4.2.2039-05). Moscow: Federal Center for Hygiene and Epidemiology of Rospotrebnadzor, 2006. 126 p. (In Russ.)]
- Bagelman S., Zvigule-Neidere G. Insight into Kytococcus schroeteri infection management: a case report and review. Infect. Dis. Rep., 2021, vol. 13, no. 1, pp. 230–238. doi: 10.3390/idr13010026
- Ballén V., Ratia C., Cepas V., Soto S.M. Enterococcus faecalis inhibits Klebsiella pneumoniae growth in polymicrobial biofilms in a glucose-enriched medium. Biofouling, 2020, vol. 36, no. 7, pp. 846–861. doi: 10.1080/08927014.2020.1824272
- Bayraktar B., Dalgic N., Duman N., Petmezci E. First case of bacteremia caused by Kytococcus schroeteri in a child with congenital adrenal hyperplasia. Pediatr. Infect. Dis. J., 2018, vol. 37, no. 12, pp. 304–305. doi: 10.1097/INF.0000000000002014
- Becker K., Schumann P., Wüllenweber J., Schulte M., Weil H.-P., Stackebrandt E., Peters G., Von Eiff C. Kytococcus schroeteri sp. nov., a novel Gram-positive actinobacterium isolated from a human clinical source. Int. J. Syst. Evol. Microbiol., 2002, vol. 52, pp. 1609–1614. doi: 10.1099/00207713-52-5-1609
- Black C.E., Costerton J.W. Current concepts regarding the effect of wound microbial ecology and biofilms on wound healing. Surg. Clin. North. Am., 2010, vol. 90, no. 6, pp. 1147–1160. doi: 10.1016/j.suc.2010.08.009
- Carek P.J., Dickerson L.M., Sack J.L. Diagnosis and management of osteomyelitis. Am. Fam. Physician., 2001, vol. 63, no. 12, pp. 2413–2420.
- Chan J.F., Wong S.S., Leung S.S., Fan R.Y., Ngan A.H., To K.K., Lau S.K., Yuen K.Y., Woo P.C. First report of chronic implant-related septic arthritis and osteomyelitis due to Kytococcus schroeteri and a review of human K. schroeteri infections. Infection, 2012, vol. 40, no. 5, pp. 567–573. doi: 10.1007/s15010-012-0250-9
- García Del Pozo E., Collazos J., Cartón J.A., Camporro D., Asensi V. Bacterial osteomyelitis: microbiological, clinical, therapeutic, and evolutive characteristics of 344 episodes. Rev. Esp. Quimioter., 2018, vol. 31, no. 3, pp. 217–225
- Gaston J.R., Andersen M.J., Johnson A.O., Bair K.L., Sullivan C.M., Guterman L.B., White A.N., Brauer A.L., Learman B.S., Flores-Mireles A.L., Armbruster C.E. Enterococcus faecalis polymicrobial interactions facilitate biofilm formation, antibiotic recalcitrance, and persistent colonization of the catheterized urinary tract. Pathogens, 2020, vol. 9, no. 10: 835. doi: 10.3390/pathogens9100835
- Kremers H.M., Nwojo M.E., Ransom J.E., Wood-Wentz C.M., Melton L.J. 3rd, Huddleston P.M. 3rd. Trends in the epidemiology of osteomyelitis: a population-based study, 1969 to 2009. J. Bone Joint Surg. Am., 2015, vol. 97, no. 10, pp. 837–845. doi: 10.2106/JBJS.N.01350
- Masters E.A., Ricciardi B.F., Bentley K.L.M., Moriarty T.F., Schwarz E.M., Muthukrishnan G. Skeletal infections: microbial pathogenesis, immunity and clinical management. Nat. Rev. Microbiol., 2022, vol. 20, no. 7, pp. 385–400. doi: 10.1038/s41579-022-00686-0
- Mundy L.M., Sahm D.F., Gilmore M. Relationships between enterococcal virulence and antimicrobial resistance. Clin. Microbiol. Rev., 2000, vol. 13, no. 4, pp. 513–522. doi: 10.1128/cmr.13.4.513-522.2000
- Noguchi K., Nishimura R., Ikawa Y., Mase S., Matsuda Y., Fujiki T., Kuroda R., Araki R., Maeba H., Yachie A. Half of Micrococcus spp. cases identified by conventional methods are revealed as other life-threatening bacteria with different drug susceptibility patterns by 16S ribosomal RNA gene sequencing. J. Infect. Chemother., 2020, vol. 26, no. 3, pp. 318–319. doi: 10.1016/j.jiac.2019.10.019
- Percival S.L., Hill K.E., Williams D.W., Hooper S.J., Thomas D.W., Costerton J.W. A review of the scientific evidence for biofilms in wounds. Wound Repair Regen., 2012, vol. 20, no. 5, pp. 647–657. doi: 10.1111/j.1524-475X.2012.00836.x
- Renvoise A., Roux V., Casalta J.P., Thuny F., Riberi A. Kytococcus schroeteri, a rare agent of endocarditis. Int. J. Infect. Dis., 2008, vol. 12, no. 2, pp. 223–227. doi: 10.1016/j.ijid.2007.06.011
- Shah A.S., Vijayvargiya P., Jung S., Wilson J.W. Postoperative hardware-related infection from Kytococcus schroeteri: its association with prosthetic material and hematological malignancies — a report of a case and review of existing literature. Case Rep. Infect. Dis., 2019: 6936472. doi: 10.1155/2019/6936472
- Shah S., Thakkar P., Poojary S., Singhal T. A case of Kytococcus schroeteri prosthetic valve endocarditis in a patient with COVID-19 infection. Indian J. Med. Microbiol., 2023, vol. 42, pp. 89–91. doi: 10.1016/j.ijmmb.2022.09.001
- Stackebrandt E., Koch C., Gvozdiak O., Schumann P. Taxonomic dissection of the genus Micrococcus: Kocuria gen. nov., Nesterenkonia gen. nov., Kytococcus gen. nov., Dermacoccus gen. nov., and Micrococcus Cohn 1872 gen. emend. Int. J. Syst. Bacteriol., 1995, vol. 45, no. 4, pp. 682–692. doi: 10.1099/00207713-45-4-682
- Tan C.A.Z., Lam L.N., Biukovic G., Soh E.Y., Toh X.W., Lemos J.A., Kline K.A. Enterococcus faecalis antagonizes Pseudomonas aeruginosa growth in mixed-species interactions. J. Bacteriol., 2022, vol. 204, no. 7: e0061521. doi: 10.1128/jb.00615-21
- Tien B.Y.Q., Goh H.M.S., Chong K.K.L., Bhaduri-Tagore S., Holec S., Dress R., Ginhoux F., Ingersoll M.A., Williams R.B.H., Kline K.A. Enterococcus faecalis promotes innate immune suppression and polymicrobial catheter-associated urinary tract infection. Infect. Immun., 2017, vol. 85, no. 12: e00378-17. doi: 10.1128/iai.00378-17
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