Antibiotic susceptibility of Tropheryma whipplei in MRC5 cells

被引:88
作者
Boulos, A [1 ]
Rolain, JM [1 ]
Raoult, D [1 ]
机构
[1] Univ Mediterranee, Fac Med, CNRS,UMR 6020, Unite Rickettsies, F-13385 Marseille 05, France
关键词
D O I
10.1128/AAC.48.3.747-752.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Whipple's disease is considered a rare chronic disease with a broad spectrum of clinical manifestations. Several antibiotics have been used for the treatment of this disease, and the current reference treatment was determined empirically on the basis of only a few clinical observations. Patients should be treated for months, and many relapse after antibiotic withdrawal. We report here the first extensive study on the susceptibilities of three reference strains of Tropheryma whipplei to antibiotic in cell culture by using a real-time PCR assay as previously described. We found that doxycycline, macrolides, ketolides, aminoglygosides, penicillin, rifampin, teicoplanin, chloramphenicol, and trimethoprim-sulfamethoxazole were active, with MICs ranging from 0.25 to 2 mug/ml. Vancomycin was somewhat active at an MIC of 10 mug/ml. We found heterogeneity in the susceptibility to imipenem, with one strain being susceptible and the two other strains being resistant. Cephalosporins, colimycine, aztreonam, and fluoroquinolones were not active. We also demonstrated that a combination of doxycycline and hydroxychloroquine was bactericidal. This combination has been shown to be active in the treatment of patients suffering from chronic infections with Coxiella burnetii, a bacterium that is also found intracellularly in acidic vacuoles. We believe, then, that this combination therapy should be further evaluated in clinical trials for the treatment of Whipple's disease.
引用
收藏
页码:747 / 752
页数:6
相关论文
共 35 条
[1]   Sequencing and analysis of the genome of the Whipple's disease bacterium Tropheryma whipplei [J].
Bentley, SD ;
Maiwald, M ;
Murphy, LD ;
Pallen, MJ ;
Yeats, CA ;
Dover, LG ;
Norbertczak, HT ;
Besra, GS ;
Quail, MA ;
Harris, DE ;
von Herbay, A ;
Goble, A ;
Rutter, S ;
Squares, R ;
Squares, S ;
Barrell, BG ;
Parkhill, J ;
Relman, DA .
LANCET, 2003, 361 (9358) :637-644
[2]   Molecular characterization of the vanE gene cluster in vancomycin-resistant Enterococcus faecalis N00-410 isolated in Canada [J].
Boyd, DA ;
Cabral, T ;
Van Caeseele, P ;
Wylie, J ;
Mulvey, MR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (06) :1977-1979
[3]   Whipple's disease, genomics, and drug therapy [J].
Cannon, WR .
LANCET, 2003, 361 (9372) :1916-1916
[4]  
DOBBINS WO, 1995, PRINCIPLES PRACTICE, P1030
[5]   Whipple disease - Clinical review of 52 cases [J].
Durand, DV ;
Lecomte, C ;
Cathebras, P ;
Rousset, H ;
Godeau, P ;
Boucher, JP ;
Simon, G ;
Dupond, JL ;
Miguet, JP ;
deWazieres, B ;
Chraibi, A ;
Dabadie, H ;
Paccalin, J ;
Bocquet, B ;
Bruhiere, J ;
Debat, P ;
Philippe, P ;
Devaux, P ;
Adam, G ;
Hillon, P ;
Massot, P ;
Cance, P ;
Waton, M ;
Levrat, R ;
Pasquier, J ;
Trepo, C ;
Falconnet, M ;
Pauchard, J ;
Gutknecht, J ;
Janbon, C ;
Barrier, JH ;
Cottin, S ;
Guillon, J ;
MagadurJoly, G ;
Allard, C ;
Dessauw, P ;
Barbier, JP ;
Bleibel, JM ;
Buge, A ;
Cabane, J ;
Haas, C ;
Huguier, M ;
Piette, AM ;
Poisson, M ;
Wechsler, B ;
Grosbois, B ;
Audigier, JC ;
Mallet, H ;
Rouhier, D ;
Rondot, P .
MEDICINE, 1997, 76 (03) :170-184
[6]   Whipple's disease in a father-daughter pair [J].
Dykman, DD ;
Cuccherini, BA ;
Fuss, IJ ;
Blum, LW ;
Woodward, JE ;
Strober, W .
DIGESTIVE DISEASES AND SCIENCES, 1999, 44 (12) :2542-2544
[7]   Whipple's disease [J].
Fenollar, F ;
Raoult, D .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (01) :1-8
[8]   Quantitative detection of Tropheryma whipplei DNA by real-time PCR [J].
Fenollar, F ;
Fournier, PE ;
Raoult, D ;
Gérolami, R ;
Lepidi, H ;
Poyart, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (03) :1119-1120
[9]   Culture of Tropheryma whipplei from human samples:: A 3-year experience (1999 to 2002) [J].
Fenollar, F ;
Birg, ML ;
Gauduchon, V ;
Raoult, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (08) :3816-3822
[10]   VanE, a new type of acquired glycopeptide resistance in Enterococcus faecalis BM4405 [J].
Fines, M ;
Perichon, B ;
Reynolds, P ;
Sahm, DF ;
Courvalin, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (09) :2161-2164