Effects of purification and fluorescent staining on viability of Mycobacterium leprae.

Over the years, researchers have carried out experiments with Mycobacterium leprae obtained from either human multibacillary lesions, or infected armadillo tissues, or infected footpad tissues of conventional mice as well as athymic nu/nu mice. In general, these sources of leprosy bacilli are satisfactory for most biochemical and mouse footpad studies, but less than satisfactory for studies in cell biology and immunology where contaminating host tissues pose a serious problem. We examined the utility of a procedure for eliminating mouse footpad tissue from M. leprae suspension using sodium hydroxide solution and its subsequent effect on the viability of the organism by determining the rate of palmitic acid oxidation, bacterial membrane integrity, and growth in the mouse footpad. We found that treating M. leprae suspension, obtained from infected nu/nu mouse footpad, with 0.1N NaOH for 3 min was sufficient to remove the majority of mouse tissue without adversely affecting the viability of the organism. This is a simple and rapid method to get suspensions of nu/nu footpad-derived viable M. leprae essentially free of host tissues, which can be a research reagent for studying the host-pathogen relationship in leprosy. We also report here a method for labeling M. leprae with the fluorescent dye PKH26, without compromising on the viability of the organism. This method may be useful in intracellular trafficking studies of M. leprae or in other cell biology studies that require tracking of the bacteria using fluorescent tag. We observed the staining to be stable in vitro over considerable lengths of time and did not affect the viability of the bacteria.

[1]  R. Lahiri,et al.  Application of a viability-staining method for Mycobacterium leprae derived from the athymic (nu/nu) mouse foot pad. , 2005, Journal of medical microbiology.

[2]  J. Holy,et al.  Mycobacterium leprae infection of human Schwann cells depends on selective host kinases and pathogen-modulated endocytic pathways , 2004 .

[3]  D. Davies,et al.  Development of a novel flow cytometric cell-mediated cytotoxicity assay using the fluorophores PKH-26 and TO-PRO-3 iodide. , 2001, Journal of immunological methods.

[4]  R. Truman,et al.  Viable M. leprae as a research reagent. , 2001, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[5]  J. Battista,et al.  Inhibition of metabolism and growth of Mycobacterium leprae by gamma irradiation. , 2000, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[6]  T. Gillis,et al.  The effect of ultraviolet light radiation on Mycobacterium leprae. , 2000, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[7]  P. Wallace,et al.  A flow cytometric method to estimate the precursor frequencies of cells proliferating in response to specific antigens. , 1999, Journal of immunological methods.

[8]  M. Shahabuddin,et al.  Plasmodium gallinaceum: fluorescent staining of zygotes and ookinetes to study malaria parasites in mosquito. , 1998, Experimental parasitology.

[9]  G. Stephanopoulos,et al.  Flow cytometric study of differentiating cultures of Bacillus subtilis. , 1995, Cytometry.

[10]  C. K. Job,et al.  The pathogenesis of leprosy in the nine-banded armadillo and the significance of IgM antibodies to PGL-1. , 1992, Indian journal of leprosy.

[11]  L. Adams,et al.  Effects of activated macrophages on Mycobacterium leprae , 1991, Infection and immunity.

[12]  G. Teare,et al.  Long-term tracking of lymphocytes in vivo: the migration of PKH-labeled lymphocytes. , 1991, Cellular immunology.

[13]  L. Sibley,et al.  Induction of unresponsiveness to gamma interferon in macrophages infected with Mycobacterium leprae , 1988, Infection and immunity.

[14]  S. Franzblau Oxidation of palmitic acid by Mycobacterium leprae in an axenic medium , 1988, Journal of clinical microbiology.

[15]  P. Brennan,et al.  Purification of phenolic glycolipid I from armadillo and human sources. , 1985, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[16]  K. Prabhakaran,et al.  Glutamic acid decarboxylase in Mycobacterium leprae , 1983, Archives of Microbiology.

[17]  P. Brennan,et al.  A novel phenolic glycolipid from Mycobacterium leprae possibly involved in immunogenicity and pathogenicity , 1981, Journal of bacteriology.

[18]  R. Rees,et al.  Effect of purification steps on the immunogenicity of Mycobacterium leprae. , 1980, British journal of experimental pathology.

[19]  J. Delville In vitro behavior of macrophages from healthy persons against M. leprae and other mycobacteria. , 1971, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[20]  R. Rees,et al.  Fate of Mycobacterium leprae in macrophages of patients with lepromatous or tuberculoid leprosy. , 1970, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

[21]  C. Shepard A brief review of experiences with short-term clinical trials monitored by mouse-foot-pad-inoculation. , 1981, Leprosy review.

[22]  D. H. McRae,et al.  A method for counting acid-fast bacteria. , 1968, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.