Clarithromycin alone and in combination with ceftriaxone inhibits the production of pneumolysin by both macrolide-susceptible and macrolide-resistant strains of Streptococcus pneumoniae

被引:40
作者
Anderson, R. [1 ]
Steel, H. C.
Cockeran, R.
Smith, A. M.
von Gottberg, A.
de Gouveia, L.
Brink, A.
Klugman, K. P.
Mitchell, T. J.
Feldman, C.
机构
[1] Univ Pretoria, Med Res Council Unit Inflammat & Immun, Dept Immunol, Fac Hlth Sci, ZA-0002 Pretoria, South Africa
[2] Natl Hlth Lab Serv, Tshwane Acad Div, Pretoria, South Africa
[3] Natl Inst Communicable Dis, MRC NICD WITS Resp & Meningeal Pathogens Res Unit, Johannesburg, South Africa
[4] Ampath Labs, Johannesburg, South Africa
[5] Emory Univ, Hubert Dept Global Hlth, Rollins Sch Publ Hlth, Sch Med, Atlanta, GA 30322 USA
[6] Emory Univ, Sch Med, Div Infect Dis, Atlanta, GA 30322 USA
[7] Univ Glasgow, Div Infect & Immun, Glasgow Biomed Res Ctr, Glasgow, Lanark, Scotland
[8] Johannesburg Hosp, Div Pulm, Dept Med, Johannesburg, South Africa
[9] Univ Witwatersrand, Johannesburg, South Africa
关键词
beta-lactam antibiotics; community-acquired pneumonia; macrolide resistance; Streptococcus pneumoniae;
D O I
10.1093/jac/dkl479
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To investigate the effects of clarithromycin (0.01-0.5 mg/L) alone or in combination with ceftriaxone (0.1 and 0.25 mg/L) on pneumolysin production by both macrolide-susceptible and -resistant [2 erm(B) positive and 2 mef(A) positive] strains of Streptococcus pneumoniae. Methods: The bacteria were cultured for 6 h at 37 degrees C/5% CO2 in tryptone soy broth, washed, enumerated and resuspended to 0.5-3 x 10(8) cfu/mL in tissue culture medium, RPMI 1640. After 16 h of incubation at 37 degrees C/5% CO2, pneumolysin was assayed in the bacteria-free supernatants, as well as in lysates, using a functional assay based on the influx of calcium into human neutrophils. Results: Exposure of not only macrolide-susceptible strains, but also the macrolide-resistant strains, of S. pneumoniae to sub-MICs of clarithromycin resulted in dose-related inhibition of the pneumolysin production, whereas production of the toxin was unaffected by ceftriaxone. Conclusions: These observations demonstrate that even in the setting of macrolide resistance the production of pneumolysin, a key virulence factor of the pneumococcus, is attenuated by exposure of this microbial pathogen to clarithromycin.
引用
收藏
页码:224 / 229
页数:6
相关论文
共 26 条
[2]  
[Anonymous], MANUAL CLIN MICROBIO
[3]  
Cockeran R, 2005, ARCH IMMUNOL THER EX, V53, P189
[4]   Proinflammatory interactions of pneumolysin with human neutrophils [J].
Cockeran, R ;
Theron, AJ ;
Steel, HC ;
Matlola, NM ;
Mitchell, TJ ;
Feldman, C ;
Anderson, R .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (04) :604-611
[5]  
Cockeran Riana, 2003, Expert Rev Anti Infect Ther, V1, P231, DOI 10.1586/14787210.1.2.231
[6]   Functional analysis of pneumolysin by use of monoclonal antibodies [J].
delosToyos, JR ;
Mendez, FJ ;
Aparicio, JF ;
Vazquez, F ;
Suarez, MD ;
Fleites, A ;
Hardisson, C ;
Morgan, PJ ;
Andrew, PW ;
Mitchell, TJ .
INFECTION AND IMMUNITY, 1996, 64 (02) :480-484
[7]  
Feldman C, 2005, PROG INFLAM RES, P49
[8]   Effects of macrolides on pneumolysin of macrolide-resistant Streptococcus pneumoniae [J].
Fukuda, Y ;
Yanagihara, K ;
Higashiyama, Y ;
Miyazaki, Y ;
Hirakata, Y ;
Mukae, H ;
Tomono, K ;
Mizuta, Y ;
Tsukamoto, K ;
Kohno, S .
EUROPEAN RESPIRATORY JOURNAL, 2006, 27 (05) :1020-1025
[9]   Pneumococcal behavior and host responses during bronchopneumonia are affected differently by the ctolytic and complement-activating activities of pneumolysin [J].
Jounblat, R ;
Kadioglu, A ;
Mitchell, TJ ;
Andrew, PW .
INFECTION AND IMMUNITY, 2003, 71 (04) :1813-1819
[10]   DIFFERENTIAL SUBSEQUENCE CONSERVATION OF INTERSPERSED REPETITIVE STREPTOCOCCUS-PNEUMONIAE BOX ELEMENTS IN DIVERSE BACTERIA [J].
KOEUTH, T ;
VERSALOVIC, J ;
LUPSKI, JR .
GENOME RESEARCH, 1995, 5 (04) :408-418