177
Diğer Gram Pozitif Koklar
1. Christensen JJ, Ruoff KL. Aerococcus, Abiotrophia and other aerobic catalase-negative gram-positive cocci. In: Jorgensen JH, Pfaller MA, eds. Manual of Clinical Microbiology. Washington,
DC: American Society for Microbiology; 2015.
2. The European Committee on Antimicrobial Susceptibility Testing. Breakpoint tables for interpretation of MICs and zone diameters (Version 13.1); 2023.
3. Clinical and Laboratory Standards Institute. Methods for Antimicrobial Dilution and Disk Susceptibility Testing of Infrequently Isolated or Fastidious Bacteria; 3rd Edition. CLSI Document M45.
Clinical and Laboratory Standards Institute, Wayne, PA; 2016.
4. Procop GW, Church DL, Hall GS, et al. Koneman’s Color Atlas and Textbook of Diagnostic Microbiology. 7th edition. Philadelphia, Wolters Kluwer; 2017.
5. Wilawer M, Elikowski W, Greberski K, Ratajska PA, Welc NA, Lisiecka ME. Abiotrophia defectiva endocarditis – Diagnostic and therapeutic challenge: Case report. IDCases 2023; 8;34:e01906.
6. Chesdachai S, Yetmar ZA, Tabaja H, et al. Contemporary experience of Abiotrophia, Granulicatella and Gemella bacteremia. J Infect 2022; 84(4): 511-517.
7. Erwes T, Godshall C. Abiotrophia defectiva meningitis following ventriculoperitoneal shunt repair: Case report and literature review. IDCases 2023; 2;31: e01708.
8. Perna A, Ricciardi L, Sturiale CL, et al. Skipped vertebral spontaneous spondylodiscitis caused by Granulicatella adiacens: Case report and a systematic literature review. J Clin Orthop Trauma
2020; 11(5): 937-941.
9. Cargill JS, Scott KS, Gascoyne-Binzi D, Sandoe JAT. Granulicatella infection: diagnosis and management. J Med Microbiol 2012; 61(Pt 6): 755-761.
10. Senn L, Entenza JM, Prod’hom G. Adherence of Abiotrophia defectiva and Granulicatella species to fibronectin: is there a link with endovascular infections? FEMS Immunol Med Microbiol
2006; 48(2): 215-7.
11. Alberti MO, Hindler JA, Humphries RM. Antimicrobial susceptibilities of Abiotrophia defectiva, Granulicatella adiacens, and Granulicatella elegans. Antimicrob Agents Chemother 2016; 60:
1411–1420.
12. Baddour LM, Wilson WR, Bayer AS, et al. American Heart Association Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in
the Young, Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and Stroke Council. Infective Endocarditis in Adults: Diagnosis, Antimicrobial Therapy, and
Management of Complications: A Scientific Statement for Healthcare Professionals From the American Heart Association. Circulation 2015; 13;132(15): 1435-86.
13. Habib G, Lancellotti P, Antunes MJ, et al. ESC Guidelines for the management of infective endocarditis: The Task Force for the Management of Infective Endocarditis of the European Society
of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the European Association of Nuclear Medicine (EANM). Eur Heart J 2015; 36: 3075-3128.
14. Rösch RM, Buschmann K, Brendel L, Schwanz T, Vahl CF. Lactococcus garvieae Endocarditis in a Prosthetic Aortic Valve: A Case Report and Literature Review. J Investig Med High Impact
Case Rep 2019; 7: 2324709619832052.
15. Shimizu A, Hase R, Suzuki D, et al. Lactococcus lactis cholangitis and bacteremia identified by MALDI-TOF mass spectrometry: A case report and review of the literature on Lactococcus lactis
infection. J Infect Chemother 2019; 25(2): 141-146.
16. Racero L, Barberis C, Traglia G, Loza MS, Vay C, Almuzara M. Infections due to Vagococcus spp. Microbiological and clinical aspects and literature review. Enferm Infecc Microbiol Clin 2021;
39(7): 335-339.
17. Matsuo T, Mori N, Kawai F, et al. Vagococcus fluvialis as a causative pathogen of bloodstream and decubitus ulcer infection: Case report and systematic review of the literature. J Infect Che-
mother 2021; 27(2): 359-363.
18. Rasmussen M. Aerococcus: an increasingly acknowledged human pathogen. Clin Microbiol Infect 2016; 22(1): 22-27.
19. Yabes JM, Perdikis S, Graham DB, Markelz A. A rare case of Aerococcus urinae infective endocarditis in an atypically young male: case report and review of the literature. BMC Infect Dis 2018;
17;18(1): 522.
20. Rougier E, Braud A, Argemi X, et al. Spondylodiscitis due to Aerococcus urinae and literature review. Infection 2018; 46(3): 419-421.
21. Lotte R, Lotte L, Degand N, et al. Infectious endocarditis caused by Helcococcus kunzii in a vascular patient: a case report and literature review. BMC Infect Dis 2015; 23; 15:238.
22. Karbuz A, Kocabaş BA, Yalman A, et al. Catheter Related Leuconostoc Mesenteroides Bacteremia: A Rare Case and Review of the Literature J Pediatr Res 2017; 4(1): 35-8.
23. Taşkapılıoğlu Ö, Bahar A, Bakar M, Yılmaz E. Nosocomial Leuconostoc Pseudomesenteroides Meningitis: A Case Report and Review of the Literature. Balkan Med J 2011; 28: 216-218
24. Miller WR, Arias CA, Murray BE. Enterococcus species, Streptococcus gallolyticus group and Leuconostoc species. In: Bennet JE, Dolin R, Blaser MJ, eds. Mandell, Douglas and Bennett’s Prin-
ciples and Practice of Infectious Diseases. Philadelphia, Elsevier; 2020.
25. Todorov SD, Dioso CM, Liong MT, Nero LA, Khosravi-Darani K, Ivanova IV. Beneficial features of pediococcus: from starter cultures and inhibitory activities to probiotic benefits. World J
Microbiol Biotechnol 2022; 8;39(1): 4.
26. Iwen PC, Mindru C, Kalil AC, Florescu DF. Pediococcus acidilactici endocarditis successfully treated with daptomycin. J Clin Microbiol 2012; 50(3): 1106-8.
27. Kim E, Yang SM, Kim HY. Weissella and the two Janus faces of the genus. Appl Microbiol Biotechnol 2023; 107(4): 1119-1127.
28. Guindo CO, Morsli M, Bellali S, Drancourt M, Grine G. A Tetragenococcus halophilus human gut isolate. Curr Res Microb Sci 2022; 16;3: 100112.
29. Furugaito M, Arai Y, Uzawa Y, et al. Antimicrobial Susceptibility to 27 Drugs and the Molecular Mechanisms of Macrolide, Tetracycline, and Quinolone Resistance in Gemella sp. Antibiotics
(Basel) 2023; 14;12(10): 1538.
30. Maraki S, Plevritaki A, Kofteridis D, et al. Bicuspid aortic valve endocarditis caused by Gemella sanguinis: Case report and literature review. J Infect Public Health 2019; 12(3): 304-308.
31. Takahashi S, Xu C, Sakai T, Fujii K, Nakamura M. Infective endocarditis following urinary tract infection caused by Globicatella sanguinis. IDCases 2017; 5;11: 18-21.
32- Miller AO, Buckwalter SP, Henry MW, et al. Globicatella sanguinis Osteomyelitis and Bacteremia: Review of an Emerging Human Pathogen with an Expanding Spectrum of Disease. Open
Forum Infect Dis 2017; 19;4(1): ofw277.
33. Hasbek M, Fırtına Topçu K, Özüm Ü. Lumbo-peritoneal Şantlı Hastada Globicatella sanguinis’e Bağlı Menenjit Olgusu [A Case of Meningitis Caused by Globicatella sanguinis in a Patient with
a Lumbo-peritoneal Shunt]. Mikrobiyol Bul 2019; 53(3): 343-347.
34. Rahmati E, Martin V, Wong D, et al. Facklamia Species as an Underrecognized Pathogen. Open Forum Infect Dis 2017; 9;4(1): ofw272.
35. Corona PS, Haddad S, Andrés J, González-López JJ, Amat C, Flores X. Case report: first report of a prosthetic joint infection caused by Facklamia hominis. Diagn Microbiol Infect Dis 2014;
80(4): 338-40.
36. Pérez-Cavazos S, Cisneros-Saldaña D, Espinosa-Villaseñor F, et al. Facklamia hominis pyelonephritis in a pediatric patient: first case report and review of the literature. Ann Clin Microbiol
Antimicrob 2022; 12;21(1): 4.
37. LaClaire L, Facklam R. Antimicrobial susceptibilities and clinical sources of Facklamia species. Antimicrob Agents Chemother 2000; 44: 2130–2132.
38. Collins MD, Lawson PA, Monasterio R, Falsen E, Sjödén B, Facklam RR. Ignavigranum ruoffiae sp. nov., isolated from human clinical specimens. Int J Syst Bacteriol 1999; 49 Pt 1: 97-101.
39. De Paulis AN, Bertona E, Gutiérrez MA, Ramírez MS, Vay CA, Predari SC. Ignavigranum ruoffiae, a rare pathogen that caused a skin abscess. JMM Case Rep 2018; 16;5(2): e005137.
40. Collins MD, Rodriguez Jovita M, Hutson RA, Falsen E, Sjödén B, Facklam RR. Dolosicoccus paucivorans gen. nov., sp. nov., isolated from human blood. Int J Syst Bacteriol 1999; 49 Pt 4: 1439-
42.
41. Mostolizadeh R, Glöckler M, Dräger A. Towards the human nasal microbiome: Simulating D. pigrum and S. aureus. Front Cell Infect Microbiol 2022; 11;12: 925215.
42. Schanz CC, Layden MP, DeSimone DC, Stevens RW, Clement J. Native mitral valve infective endocarditis due to Dolosigranulum pigrum. IDCases 2023; 12;33: e01818.
43. Laclaire L, Facklam R. Antimicrobial susceptibility and clinical sources of Dolosigranulum pigrum cultures. Antimicrob Agents Chemother 2000; 44(7): 2001-3.
44. Baiano JC, Barnes AC. Towards control of Streptococcus iniae. Emerg Infect Dis 2009; 15(12): 1891-6.
45. Becker K, Skov RL, Von Eiff C. Staphylococcus, Micrococcus, and other catalase-postive cocci. In: Jorgensen JH, Pfaller MA, eds. Manual of Clinical Microbiology. Washington, DC: American
Society for Microbiology; 2015.
46. Zhu M, Zhu Q, Yang Z, Liang Z. Clinical Characteristics of Patients with Micrococcus luteus Bloodstream Infection in a Chinese Tertiary-Care Hospital. Pol J Microbiol 2021; 70(3): 321-326.
47. Mandviya P, Ghanwate N, Thakare P. First case report of isolation of Micrococcus lylae from urinary catheter of a 50-year-old woman suffering from malignancy. J Infect Dev Ctries 2023;
27;17(7): 1041-1046.
48. Ziogou A, Giannakodimos I, Giannakodimos A, Baliou S, Ioannou P. Kocuria Species Infections in Humans-A Narrative Review. Microorganisms 2023; 21;11(9): 2362.
49. Kandi V, Palange P, Vaish R, et al. Emerging Bacterial Infection: Identification and Clinical Significance of Kocuria Species. Cureus 2016; 10;8(8): e731.
50. Odeberg G, Bläckberg A, Sunnerhagen T. Infection or Contamination with Rothia, Kocuria, Arthrobacter and Pseudoglutamicibacter-a Retrospective Observational Study of Non-Micrococcus
Micrococcaceae in the Clinic. J Clin Microbiol 2023; 20;61(4): e0148422.
51. Živković Zarić RS, Pejčić AV, Janković SM, et al. Antimicrobial treatment of Kocuria kristinae invasive infections: Systematic review. J Chemother 2019; 31(3): 109-119.
52. Lappan R, Jamieson SE and Peacock CS. Reviewing the Pathogenic Potential of the Otitis-Associated Bacteria Alloiococcus otitidis and Turicella otitidis. Front Cell Infect Microbiol 2020; 10:51.
53. Fatahi-Bafghi M. Characterization of the Rothia spp. and their role in human clinical infections. Infect Genet Evol 2021; 93: 104877.
54. Franconieri F, Join-Lambert O, Creveuil C, et al. Rothia spp. infective endocarditis: A systematic literature review. Infect Dis Now 2021; 51(3): 22
