Cholesterol oxidase from Rhodococcus equi is likely the major factor involved in the cooperative lytic process (CAMP reaction) with Listeria monocytogenes

J.F. FERNÁNDEZ‐GARAYZÁBAL, C. DELGADO, M.M. BLANCO, G. SUÁREZ AND L. DOMÍNGUEZ. 1996. The CAMP reaction between Listeria monocytogenes and Rhodococcus equi was studied by a diffusion assay. Listeria monocytogenes displayed identical cooperative haemolytic effect with supernatant cultures of equi or with commercial cholesterol oxidase (COX). This result, even with enzymes of different sources (commercial COX is obtained from Pseudomonas spp.) suggests that this enzyme secreted by R. equi has a crucial role in the synergistic haemolytic (CAMP) reaction with L. monocytogenes. The mechanism of the cooperative lytic process between L. monocytogenes and R. equi may represent a different and novel mechanism reaction, in which the COX may not act as a conventional second‐step factor, and a reaction different to the direct interaction with the cholesterol of the erythrocyte membrane may be involved.

[1]  J. Alouf,et al.  The sulphydryl-activated cytolysin and a sphingomyelinase C are the major membrane-damaging factors involved in cooperative (CAMP-like) haemolysis of Listeria spp. , 1995, Research in microbiology.

[2]  R. Mckellar Use of the CAMP test for identification of Listeria monocytogenes , 1994, Applied and environmental microbiology.

[3]  M. Delgado Factores modificantes del fenotipo hemolítico de listeria. Efecto camp , 1994 .

[4]  J. Vázquez-Boland,et al.  Listeria monocytogenes CAMP reaction , 1992, Clinical Microbiology Reviews.

[5]  J. Vázquez-Boland,et al.  Role of potassium tellurite and brain heart infusion in expression of the hemolytic phenotype of Listeria spp. on agar plates , 1992, Applied and environmental microbiology.

[6]  J. Vázquez-Boland,et al.  Revision of the validity of CAMP tests for Listeria identification. Proposal of an alternative method for the determination of haemolytic activity by Listeria strains. , 1990, Acta microbiologica Hungarica.

[7]  J. Blanco,et al.  A technique for the direct identification of haemolytic‐pathogenic listeria on selective plating media , 1989 .

[8]  E. Gómez-Lucia,et al.  Microplate technique to determine hemolytic activity for routine typing of Listeria strains , 1986, Journal of clinical microbiology.

[9]  Heinrich J.G. Matthies,et al.  Cholesterol oxidase susceptibility of the red cell membrane. , 1984, Biochimica et biophysica acta.

[10]  A. W. Bernheimer,et al.  Action of bacterial cytotoxins on normal mammalian cells and cells with altered membrane lipid composition. , 1984, Toxicon : official journal of the International Society on Toxinology.

[11]  B. Skalka,et al.  Routine test for in vitro differentiation of pathogenic and apathogenic Listeria monocytogenes strains , 1982, Journal of clinical microbiology.

[12]  H. Nemoto,et al.  Synergistic hemolysis phenomenon of Listeria monocytogenes and Corynebacterium equi. , 1980, Nihon juigaku zasshi. The Japanese journal of veterinary science.

[13]  A. W. Bernheimer,et al.  Stepwise degradation of membrane sphingomyelin by corynebacterial phospholipases , 1980, Infection and immunity.

[14]  Y. Barenholz,et al.  Cholesterol oxidase as a probe for studying membrane organisation , 1978, Nature.

[15]  M. Gottlieb The reactivity of human erythrocyte membrane cholesterol with a cholesterol oxidase. , 1977, Biochimica et biophysica acta.