Ruminococcus gnavus bacteraemia in a patient with multiple haematological malignancies

References

1. Qin J, Li R, Raes J, Arumugam M, Burgdorf KS et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature 2010; 464:59–65 [View Article]
   [Google Scholar]
2. Fontanals D, Larruzea A, Sanfeliu I. Direct identification of Ruminococcus gnavus by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) on a positive anaerobic blood culture bottle. Anaerobe 2018; 54:264–266 [View Article]
   [Google Scholar]
3. Lefever S, Van Den Bossche D, Van Moerkercke W, D’Hondt M, Alegret Pampols MdelC et al. Ruminococcus gnavus bacteremia, an uncommon presentation of a common member of the human gut microbiota: case report and literature review. Acta Clin Belg 2018; 7:1–4 [View Article]
   [Google Scholar]
4. Roux A-L, El Sayed F, Duffiet P, Bauer T, Heym B et al. Ruminococcus gnavus total hip arthroplasty infection in a 62-year-old man with ulcerative colitis. J Clin Microbiol 2015; 53:1428–1430 [View Article]
   [Google Scholar]
5. Hansen SGK, Skov MN, Justesen US. Two cases of Ruminococcus gnavus bacteremia associated with diverticulitis. J Clin Microbiol 2013; 51:1334–1336 [View Article]
   [Google Scholar]
6. Kim YJ, Kang HY, Han Y, Lee MS, Lee HJ et al. A bloodstream infection by Ruminococcus gnavus in a patient with a gall bladder perforation. Anaerobe 2017; 47:129–131 [View Article]
   [Google Scholar]
7. Titécat M, Wallet F, Vieillard M-H, Courcol RJ, Loïez C et al. Ruminococcus gnavus: an unusual pathogen in septic arthritis. Anaerobe 2014; 30:159–160 [View Article]
   [Google Scholar]
8. Fernández-Caso B, García D, Domingo L et al. Ruminococcus gnavus infection of a metal-on-metal hip arthroplasty resembling a pseudotumor in a 72 year-old woman with no gastrointestinal symptoms. Enfermedades Infecc y Microbiol Clin 2017; 35:540–541
   [Google Scholar]
9. Solís RA, Salas CM, Victoria M, Arrieta A. Prosthetic joint infection by Ruminococcus gnavus in a patient without associated digestive symptoms. Med Clínica 2017; 148:7–8
   [Google Scholar]
10. Machiels K, Sabino J, Vandermosten L, Joossens M, Arijs I et al. Specific members of the predominant gut microbiota predict pouchitis following colectomy and IpaA in UC. Gut 2017; 66:79–88 [View Article]
    [Google Scholar]
11. Sokol H, Jegou S, McQuitty C et al. Specificities of the intestinal microbiota in patients with inflammatory bowel disease and Clostridium difficile infection. Gut Microbes 2017; 0976:1–6
    [Google Scholar]
12. Breban M, Tap J, Leboime A, Said-Nahal R, Langella P et al. Faecal microbiota study reveals specific dysbiosis in spondyloarthritis. Ann Rheum Dis 2017; 76:1614–1622 [View Article]
    [Google Scholar]
13. Chua H-H, Chou H-C, Tung Y-L, Chiang B-L, Liao C-C et al. Intestinal dysbiosis featuring abundance of Ruminococcus gnavus associates with allergic diseases in infants. Gastroenterology 2018; 154:154–167 [View Article]
    [Google Scholar]
14. Zheng H, Liang H, Wang Y, Miao M, Shi T et al. Altered gut microbiota composition associated with eczema in infants. PLoS One 2016; 11:e0166026–13 [View Article]
    [Google Scholar]
15. Berry D, Reinisch W. Intestinal microbiota: a source of novel biomarkers in inflammatory bowel diseases?. Best Pract Res Clin Gastroenterol 2013; 27:47–58 [View Article]
    [Google Scholar]
16. Nucci M, Anaissie E. Infections in patients with multiple myeloma in the era of high-dose therapy and novel agents. Clin Infect Dis 2009; 49:1211–1225 [View Article]
    [Google Scholar]
17. Blimark C, Holmberg E, Mellqvist U-H, Landgren O, Björkholm M et al. Multiple myeloma and infections: a population-based study on 9253 multiple myeloma patients. Haematologica 2015; 100:107–113 [View Article]
    [Google Scholar]
18. Pomeroy C, Oken MM, Rydell RE, Filice GA. Infection in the myelodysplastic syndromes. Am J Med 1991; 90:338–344 [View Article]
    [Google Scholar]
19. Boogaerts MA, Nelissen V, Roelant C, Goossens W. Blood neutrophil function in primary myelodysplastic syndromes. Br J Haematol 1983; 55:217–227 [View Article]
    [Google Scholar]
20. Stuck AE, Minder CE, Frey FJ. Risk of infectious complications in patients taking glucocorticosteroids. Clin Infect Dis 1989; 11:954–963 [View Article]
    [Google Scholar]
21. Crost EH, Tailford LE, Le Gall G, Fons M, Henrissat B et al. Utilisation of mucin glycans by the human gut symbiont Ruminococcus gnavus is strain-dependent. PLoS One 2013; 8:e76341 [View Article]
    [Google Scholar]
22. Beaud D, Tailliez P, Anba-Mondoloni J. Genetic characterization of the beta-glucuronidase enzyme from a human intestinal bacterium, Ruminococcus gnavus . Microbiology 2005; 151:2323–2330 [View Article]
    [Google Scholar]
23. Nishino K, Nishida A, Inoue R, Kawada Y, Ohno M et al. Analysis of endoscopic brush samples identified mucosa-associated dysbiosis in inflammatory bowel disease. J Gastroenterol 2018; 53:95–106 [View Article]
    [Google Scholar]
24. Hall AB, Yassour M, Sauk J, Garner A, Jiang X et al. A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients. Genome Med 2017; 9:1–12 [View Article]
    [Google Scholar]
25. Joossens M, Huys G, Cnockaert M, De Preter V, Verbeke K et al. Dysbiosis of the faecal microbiota in patients with Crohn's disease and their unaffected relatives. Gut 2011; 60:631–637 [View Article]
    [Google Scholar]
26. Ubeda C, Pamer EG. Antibiotics, microbiota, and immune defense. Trends Immunol 2012; 33:459–466 [View Article]
    [Google Scholar]
27. Brown RL, Clarke TB. The regulation of host defences to infection by the microbiota. Immunology 2017; 150:1–6 [View Article]
    [Google Scholar]
28. Hooper LV, Littman DR, Macpherson AJ. Interactions between the microbiota and the immune system. Science 2012; 336:1268–1273 [View Article]
    [Google Scholar]
29. Taur Y, Pamer EG. The intestinal microbiota and susceptibility to infection in immunocompromised patients. Curr Opin Infect Dis 2013; 26:332–337 [View Article]
    [Google Scholar]
30. Lagacé-Wiens PRS, Adam HJ, Karlowsky JA, Nichol KA, Pang PF et al. Identification of blood culture isolates directly from positive blood cultures by use of matrix-assisted laser desorption ionization-time of flight mass spectrometry and a commercial extraction system: analysis of performance, cost, and turnaround time. J Clin Microbiol 2012; 50:3324–3328 [View Article]
    [Google Scholar]