Can intracellular Staphylococcus aureus in osteomyelitis be treated using current antibiotics? A systematic review and narrative synthesis

被引:47
作者
Zelmer, Anja R. [1 ]
Nelson, Renjy [2 ,3 ]
Richter, Katharina [4 ]
Atkins, Gerald J. [1 ]
机构
[1] Univ Adelaide, Fac Hlth & Med Sci, Ctr Orthopaed & Trauma Res, Adelaide, SA 5000, Australia
[2] Cent Adelaide Local Hlth Network, Dept Infect Dis, Adelaide, SA 5000, Australia
[3] Royal Adelaide Hosp, Adelaide, SA 5000, Australia
[4] Univ Adelaide, Basil Hetzel Inst Translat Hlth Res, Dept Surg, Richter Lab, Adelaide, SA 5011, Australia
关键词
SMALL-COLONY VARIANTS; PROSTHETIC JOINT INFECTIONS; FUSIDIC ACID; PHARMACODYNAMIC EVALUATION; IN-VITRO; STREPTOCOCCUS-PNEUMONIAE; LISTERIA-MONOCYTOGENES; DELIVERY-SYSTEM; DRUG-DELIVERY; CLINICAL-USE;
D O I
10.1038/s41413-022-00227-8
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Approximately 40% of treatments of chronic and recurrent osteomyelitis fail in part due to bacterial persistence. Staphylococcus aureus, the predominant pathogen in human osteomyelitis, is known to persist by phenotypic adaptation as small-colony variants (SCVs) and by formation of intracellular reservoirs, including those in major bone cell types, reducing susceptibility to antibiotics. Intracellular infections with S. aureus are difficult to treat; however, there are no evidence-based clinical guidelines addressing these infections in osteomyelitis. We conducted a systematic review of the literature to determine the demonstrated efficacy of all antibiotics against intracellular S. aureus relevant to osteomyelitis, including protein biosynthesis inhibitors (lincosamides, streptogramins, macrolides, oxazolidines, tetracyclines, fusidic acid, and aminoglycosides), enzyme inhibitors (fluoroquinolones and ansamycines), and cell wall inhibitors (beta-lactam inhibitors, glycopeptides, fosfomycin, and lipopeptides). The PubMed and Embase databases were screened for articles related to intracellular S. aureus infections that compared the effectiveness of multiple antibiotics or a single antibiotic together with another treatment, which resulted in 34 full-text articles fitting the inclusion criteria. The combined findings of these studies were largely inconclusive, most likely due to the plethora of methodologies utilized. Therefore, the reported findings in the context of the models employed and possible solutions for improved understanding are explored here. While rifampicin, oritavancin, linezolid, moxifloxacin and oxacillin were identified as the most effective potential intracellular treatments, the scientific evidence for these is still relatively weak. We advocate for more standardized research on determining the intracellular effectiveness of antibiotics in S. aureus osteomyelitis to improve treatments and patient outcomes.
引用
收藏
页数:18
相关论文
共 191 条
  • [21] Detection of the mec-A gene and phenotypic detection of resistance in Staphylococcus aureus isolates with borderline or low-level methicillin resistance
    Bignardi, GE
    Woodford, N
    Chapman, A
    Johnson, AP
    Speller, DCE
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 (01) : 53 - 63
  • [22] Developments in Glycopeptide Antibiotics
    Blaskovich, Mark A. T.
    Hansford, Karl A.
    Butler, Mark S.
    Jia, ZhiGuang
    Mark, Alan E.
    Cooper, Matthew A.
    [J]. ACS INFECTIOUS DISEASES, 2018, 4 (05): : 715 - 735
  • [23] The macrolides
    Blondeau, JM
    DeCarolis, E
    Metzler, KL
    Hansen, GT
    [J]. EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2002, 11 (02) : 189 - 215
  • [24] Fluoroquinolones: Mechanism of action, classification, and development of resistance
    Blondeau, JM
    [J]. SURVEY OF OPHTHALMOLOGY, 2004, 49 : S73 - S78
  • [25] Intracellular Penetration and Effects of Antibiotics on Staphylococcus aureus Inside Human Neutrophils: A Comprehensive Review
    Bongers, Suzanne
    Hellebrekers, Pien
    Leenen, Luke P. H.
    Koenderman, Leo
    Hietbrink, Falco
    [J]. ANTIBIOTICS-BASEL, 2019, 8 (02):
  • [26] Clindamycin combination treatment for the treatment of bone and joint infections caused by clindamycin-susceptible, erythromycin-resistant Staphylococcus spp.
    Bonnaire, Agathe
    Vernet-Garnier, Veronique
    Lebrun, Delphine
    Bajolet, Odile
    Bonnet, Morgane
    Hentzien, Maxime
    Ohl, Xavier
    Diallo, Saidou
    Bani-Sadr, Firouze
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2021, 99 (01)
  • [27] Internalization of bacteria by osteoblasts in a patient with recurrent, long-term osteomyelitis - A case report
    Bosse, MJ
    Gruber, HE
    Ramp, WK
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2005, 87A (06) : 1343 - 1347
  • [28] Population pharmacokinetics of clindamycin orally and intravenously administered in patients with osteomyelitis
    Bouazza, Naim
    Pestre, Vincent
    Jullien, Vincent
    Curis, Emmanuel
    Urien, Saik
    Salmon, Dominique
    Treluyer, Jean-Marc
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2012, 74 (06) : 971 - 977
  • [29] Oxazolidinones: activity, mode of action, and mechanism of resistance
    Bozdogan, B
    Appelbaum, PC
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 23 (02) : 113 - 119
  • [30] Pharmacodynamics and pharmacokinetics of spiramycin and their clinical significance
    Brook, I
    [J]. CLINICAL PHARMACOKINETICS, 1998, 34 (04) : 303 - 310