Decrease of virulence for BALB/c mice produced by continuous subculturing of Nocardia brasiliensis

被引:11
作者
Almaguer-Chavez, Janeth A. [1 ]
Welsh, Oliverio [1 ]
Lozano-Garza, Hector G. [2 ]
Said-Fernandez, Salvador [2 ]
Romero-Diaz, Viktor J. [3 ]
Ocampo-Candiani, Jorge [1 ]
Vera-Cabrera, Lucio [1 ]
机构
[1] Hosp Univ Jose E Gonzalez, Serv Dermatol, Monterrey 64460, NL, Mexico
[2] IMSS, Ctr Invest Biomed Noreste, Monterrey 64460, NL, Mexico
[3] UANL, Fac Med, Dept Histol, Monterrey 64460, NL, Mexico
来源
BMC INFECTIOUS DISEASES | 2011年 / 11卷
关键词
Mycetoma; Nocardia; attenuation; MYCOBACTERIUM-BOVIS BCG; EXPERIMENTAL ACTINOMYCETOMA; INFECTIONS; ADAPTATION; MYCETOMA; PROTEASE; SUBSETS;
D O I
10.1186/1471-2334-11-290
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Subculturing has been extensively used to attenuate human pathogens. In this work we studied the effect of continuous subculturing of Nocardia brasiliensis HUJEG-1 on virulence in a murine model. Methods: Nocardia brasiliensis HUJEG-1 was subcultured up to 130 times on brain heart infusion over four years. BALB/c mice were inoculated in the right foot pad with the bacteria subcultured 0, 40, 80, 100 and 130 times (T(0), T(40), T(80) T(100) and T(130)). The induction of resistance was tested by using T(130) to inoculate a group of mice followed by challenge with T0 12 weeks later. Biopsies were taken from the newly infected foot-pad and immunostained with antibodies against CD4, CD8 and CD14 in order to analyze the in situ immunological changes. Results: When using T(40), T(80) T(100) and T(130) as inoculums we observed lesions in 10, 5, 0 and 0 percent of the animals, respectively, at the end of 12 weeks. In contrast, their controls produced mycetoma in 80, 80, 70 and 60% of the inoculated animals. When studying the protection of T(130), we observed a partial resistance to the infection. Immunostaining revealed an intense CD4+ lymphocytic and macrophage infiltrate in healing lesions. Conclusions: After 130 in vitro passages of N. brasiliensis HUJEG-1 a severe decrease in its virulence was observed. Immunization of BALB/c mice, with these attenuated cells, produced a state of partial resistance to infection with the non-subcultured isolate.
引用
收藏
页数:8
相关论文
共 16 条
[1]   Efficacy of DA-7218, a new oxazolidinone prodrug, in the treatment of experimental actinomycetoma produced by Nocardia brasiliensis [J].
Alejandra Espinoza-Gonzalez, Nelly ;
Welsh, Oliverio ;
Waksman de Torres, Noemi ;
Cavazos-Rocha, Norma ;
Ocampo-Candiani, Jorge ;
Said-Fernandez, Salvador ;
Lozano-Garza, Gerardo ;
Choi, Sung-Hak ;
Vera-Cabrera, Lucio .
MOLECULES, 2008, 13 (01) :31-40
[2]   Genome evolution and adaptation in a long-term experiment with Escherichia coli [J].
Barrick, Jeffrey E. ;
Yu, Dong Su ;
Yoon, Sung Ho ;
Jeong, Haeyoung ;
Oh, Tae Kwang ;
Schneider, Dominique ;
Lenski, Richard E. ;
Kim, Jihyun F. .
NATURE, 2009, 461 (7268) :1243-U74
[3]  
CALMETTE A, 1927, MASSON CO EDITEURS L, V120
[4]   Experimental Adaptation of Burkholderia cenocepacia to Onion Medium Reduces Host Range [J].
Ellis, Crystal N. ;
Cooper, Vaughn S. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2010, 76 (08) :2387-2396
[5]  
FOLB PI, 1976, INFECT IMMUN, V13, P1490, DOI 10.1128/IAI.13.5.1490-1496.1976
[6]   NOCARDIA INFECTIONS IN CONGENITALLY ATHYMIC (NUDE) MICE AND IN OTHER INBRED MOUSE STRAINS [J].
FOLB, PI ;
TIMME, A ;
HOROWITZ, A .
INFECTION AND IMMUNITY, 1977, 18 (02) :459-466
[7]   IgM but not IgG monoclonal anti-Nocardia brasiliensis antibodies confer protection against experimental actinomycetoma in BALB/c mice [J].
Gonzalez-Suarez, Maria L. ;
Salinas-Carmona, Mario C. ;
Perez-Rivera, Isabel .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2009, 57 (01) :17-24
[8]   Lymphocyte subsets, macrophages and Langerhans cells in actinomycetoma and eumycetoma tissue reaction [J].
Guimaraes, CC ;
Castro, LGM ;
Sotto, MN .
ACTA TROPICA, 2003, 87 (03) :377-384
[9]   Immunogenicity and biophysical properties of a Nocardia brasiliensis protease involved in pathogenesis of mycetoma [J].
Licón-Trillo, A ;
Castro-Corona, MA ;
Salinas-Carmona, MC .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2003, 37 (01) :37-44
[10]  
Lopez Martinez R, 1992, Gac Med Mex, V128, P477