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Home All issues Volume 38 / No 12 (Décembre 2022) Med Sci (Paris), 38 12 (2022) 1043-1051 References
Open Access
Issue
Med Sci (Paris)
Volume 38, Number 12, Décembre 2022
Un monde de virus
Page(s) 1043 - 1051
Section M/S Revues
DOI https://doi.org/10.1051/medsci/2022169
Published online 13 December 2022
  1. Ackermann HW. 5500 Phages examined in the electron microscope. Arch Virol 2007 ; 152 : 227–243. [CrossRef] [PubMed] [Google Scholar]
  2. Bergh Ø. BØrsheim KY, Bratbak G, Heldal M. High abundance of viruses found in aquatic environments. Nature 1989 ; 340 : 467–468. [Google Scholar]
  3. Summers WC. Bacteriophage therapy. Annu Rev Microbiol 2001 ; 55 : 437–451. [CrossRef] [PubMed] [Google Scholar]
  4. Ferry T, Kolenda C, Gustave CAet al. Phage therapy in bone and joint infection : history, scientific basis, feasibility and perspectives in France. Virologie 2018 ; 24 : 4–11. [Google Scholar]
  5. Pirnay JP, Verbeken G, Ceyssens PJet al. The Magistral Phage. Viruses 2018 ; 10. [Google Scholar]
  6. Ferry T, Kolenda C, Briot T, et al. Implementation of a complex bone and joint infection phage therapy centre in France : Lessons to be learned after 4 years’ experience. Clin Microbiol Infect 2021; S1198-743X(21)00556-5. [PubMed] [Google Scholar]
  7. Chen Y, Batra H, Dong Jet al. Genetic Engineering of Bacteriophages against infectious diseases. Front Microbiol 2019 ; 10 : 954. [CrossRef] [PubMed] [Google Scholar]
  8. Fauconnier A.. Phage therapy regulation : from night to dawn. Viruses 2019 ; 11 : E352. [Google Scholar]
  9. Merabishvili M, Pirnay JP, Verbeken Get al. Quality-controlled small-scale production of a well-defined bacteriophage cocktail for use in human clinical trials. PloS One 2009 ; 4 : e4944. [Google Scholar]
  10. World Medical Association World medical association declaration of Helsinki : ethical principles for medical research involving human subjects. JAMA 2013 ; 310 : 2191–2194. [CrossRef] [PubMed] [Google Scholar]
  11. Tamma PD, Aitken SL, Bonomo RA, et al. Infectious Diseases Society of America 2022 guidance on the treatment of extended-Spectrum β-lactamase producing enterobacterales (ESBL-E), carbapenem-resistant enterobacterales (CRE), and Pseudomonas aeruginosa with difficult-to-treat resistance (DTR-P. aeruginosa). Clin Infect Dis 2022; ciac268. [Google Scholar]
  12. Lood C, Boeckaerts D, Stock M, et al. Digital phagograms : predicting phage infectivity through a multilayer machine learning approach. Curr Opin Virol 2022; 52 : 174–81. [CrossRef] [PubMed] [Google Scholar]
  13. Schooley RT, Biswas B, Gill JJet al. Development and use of personalized bacteriophage-based therapeutic cocktails to treat a patient with a disseminated resistant Acinetobacter baumannii Infection. Antimicrob Agents Chemother 2017 ; 61. [CrossRef] [PubMed] [Google Scholar]
  14. Djebara S, Maussen C, De Vos D, et al. Processing phage therapy requests in a Brussels military hospital : Lessons identified. Viruses 2019 17; 11(3) [Google Scholar]
  15. Jault P, Leclerc T, Jennes Set al. Efficacy and tolerability of a cocktail of bacteriophages to treat burn wounds infected by Pseudomonas aeruginosa (PhagoBurn): a randomised, controlled, double-blind phase 1/2 trial. Lancet Infect Dis 2019 ; 19 : 35–45. [Google Scholar]
  16. Law N, Logan C, Yung Get al. Successful adjunctive use of bacteriophage therapy for treatment of multidrug-resistant Pseudomonas aeruginosa infection in a cystic fibrosis patient. Infection 2019 ; 47 : 665–668. [CrossRef] [PubMed] [Google Scholar]
  17. Chen P, Liu Z, Tan X, et al. Bacteriophage therapy for empyema caused by carbapenem-resistant Pseudomonas aeruginosa. Biosci Trends 2022; 16 : 158–62. [CrossRef] [PubMed] [Google Scholar]
  18. Dedrick RM, Guerrero-Bustamante CA, Garlena RAet al. Engineered bacteriophages for treatment of a patient with a disseminated drug-resistant Mycobacterium abscessus. Nat Med 2019 ; 25 : 730–733. [Google Scholar]
  19. Ferry T, Kolenda C, Briot T, et al. Past and future of phage therapy and phage-derived proteins in patients with bone and joint infection. Viruses 2021; 13 : 2414. [Google Scholar]
  20. Ferry T, Kolenda C, Batailler C, et al. Phage therapy as adjuvant to conservative surgery and antibiotics to salvage patients with relapsing S. aureus prosthetic knee infection. Front Med 2020; 7 : 570572. [CrossRef] [Google Scholar]
  21. Kolenda C, Josse J, Medina M, et al. Evaluation of the activity of a combination of three bacteriophages alone or in association with antibiotics on Staphylococcus aureus embedded in biofilm or internalized in osteoblasts. Antimicrob Agents Chemother 2020 21; 64. [Google Scholar]
  22. Ferry T, Seng P, Mainard Det al. The CRIOAc healthcare network in France : A nationwide Health Ministry program to improve the management of bone and joint infection. Orthop Traumatol Surg Res 2019 ; 105 : 185–190. [Google Scholar]
  23. Ferry T, Kolenda C, Batailler C, et al. Case report : Arthroscopic “Debridement Antibiotics and Implant Retention” with local injection of personalized phage therapy to salvage a relapsing Pseudomonas aeruginosa prosthetic knee infection. Front Med 2021; 8 : 569159. [CrossRef] [Google Scholar]
  24. Leitner L, Ujmajuridze A, Chanishvili N, et al. Intravesical bacteriophages for treating urinary tract infections in patients undergoing transurethral resection of the prostate : a randomised, placebo-controlled, double-blind clinical trial. Lancet Infect Dis 2021; 21 : 427–36. [Google Scholar]
  25. Javaudin F, Latour C, Debarbieux L, Lamy-Besnier Q. Intestinal bacteriophage therapy : Looking for optimal efficacy. Clin Microbiol Rev 2021; 34 : e0013621. [CrossRef] [PubMed] [Google Scholar]
  26. Marcuk LM, Nikiforov VN, Scerbak JFet al. Clinical studies of the use of bacteriophage in the treatment of cholera. Bull World Health Organ 1971 ; 45 : 77–83. [PubMed] [Google Scholar]
  27. Sarker SA, Sultana S, Reuteler Get al. Oral phage therapy of acute bacterial diarrhea with two coliphage preparations : A randomized trial in children From Bangladesh. EBioMedicine 2016 ; 4 : 124–137. [CrossRef] [PubMed] [Google Scholar]
  28. Corbellino M, Kieffer N, Kutateladze M, et al. Eradication of a multidrug-Resistant, carbapenemase-producing Klebsiella pneumoniae isolate following oral and intra-rectal therapy with a custom made, lytic bacteriophage preparation. Clin Infect Dis 2020; 70 : 1998–2001. [CrossRef] [PubMed] [Google Scholar]
  29. Riedel T, Wittmann J, Bunk Bet al. A Clostridioides difficile bacteriophage genome encodes functional binary toxin-associated genes. J Biotechnol 2017 ; 250 : 23–28. [CrossRef] [PubMed] [Google Scholar]
  30. Nale JY, Spencer J, Hargreaves KRet al. Bacteriophage combinations significantly reduce Clostridium difficile growth in vitro and proliferation in vivo. Antimicrob Agents Chemother 2016 ; 60 : 968–981. [CrossRef] [PubMed] [Google Scholar]
  31. Selle K, Fletcher JR, Tuson H, et al. in vivo targeting of Clostridioides difficile using phage-delivered CRISPR-Cas3 antimicrobials. mBio 2020; 11 : e00019–20. [Google Scholar]
  32. Park H, Laffin MR, Jovel Jet al. The success of fecal microbial transplantation in Clostridium difficile infection correlates with bacteriophage relative abundance in the donor : a retrospective cohort study. Gut Microbes 2019 ; 10 : 676–687. [CrossRef] [PubMed] [Google Scholar]
  33. Zuo T, Wong SH, Lam Ket al. Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome. Gut 2018 ; 67 : 634–643. [PubMed] [Google Scholar]
  34. Ott SJ, Waetzig GH, Rehman Aet al. Efficacy of sterile fecal filtrate transfer for treating patients with Clostridium difficile infection. Gastroenterology 2017 ; 152 : 799–811 e7. [Google Scholar]
  35. Norman JM, Handley SA, Baldridge MTet al. Disease-specific alterations in the enteric virome in inflammatory bowel disease. Cell 2015 ; 160 : 447–460. [CrossRef] [PubMed] [Google Scholar]
  36. Clooney AG, Sutton TDS, Shkoporov ANet al. Whole-virome analysis sheds light on viral dark matter in inflammatory bowel disease. Cell Host Microbe 2019 ; 26 : 764–78.e5. [CrossRef] [PubMed] [Google Scholar]
  37. Tarris G, de Rougemont A, Charkaoui M, et al. Enteric Viruses and inflammatory bowel disease. Viruses 2021; 13 : 104. [Google Scholar]
  38. Ferry T, Kolenda C, Gustave CA, et al. Phagothérapie pour les patients présentant une infection ostéoarticulaire : historique, fondements, faisabilité et perspectives en France. Virologie (Montrouge) 2020; 24 : 49–56. [Google Scholar]

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