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Experimental central nervous system phaeohyphomycosis following intranasal inoculation of Xylohypha bantiana in cortisone-treated mice

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Abstract

Experimental central nervous system (CNS) phaeohyphomycosis was established in cortisone-treated mice following intranasal exposure to conidia of Xylohypha bantiana (Cladosporium bantianum, C. trichoides). X. bantiana was recovered from the lungs of 78% of intranasally inoculated normal mice sacrificed within the first 3 days of infection and from 15% at day 28. The fungus was not recovered from the brains of normal mice. In contrast, X. bantiana was recovered from only 33% of the lungs of cortisone-treated mice within the first 3 days of infection. However, the fungus was recovered from the brains of 11% of cortisone-treated mice sacrificed or dying over a 28 day period. Histologically and temporally the CNS disease in cortisone-treated, intranasally inoculated mice was consistent with hematogenous dissemination from a primary pulmonary focus.

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References

  1. Apabuukuu AA. Reactive processes in the early stages of brain mycosis. In Russian. Arkiv Patologii 1968; 30:17–23.

    Google Scholar 

  2. Aravyski RA, Aronson VB. Comparative histopathology of chromomycosis and cladosporiosis in the experiment. Mycopathol et Mycol Applicata 1968; 36:322–340.

    Google Scholar 

  3. Claesson MH, Ropke C. Colony formation by subpopulations of T lymphocytes. IV. Inhibitory effect of hydrocortisone on human and murine T cell subsets. Clin Exper Immunol 1983; 54:554–560.

    Google Scholar 

  4. De Mello MT, Cedillos RA, De Jimeniz GG, Trejos A. Infeccion in vitro e in vivo de histiocitos alveolares por Cladosporium trichoides, agente de abscesos cerebrales en el hombre. Anais de Microbiologia 1964; 12:75–84.

    Google Scholar 

  5. Dixon DM, Shadomy HJ, Shadomy S. Isolation of Cladosporium trichoides from nature. Mycopathologia 1977; 62:125–127.

    Google Scholar 

  6. Dixon DM, Shadomy HJ, Shadomy S. Dematiaceous fungal pathogens isolated from nature. Mycopathologia 1980; 70:153–161.

    Google Scholar 

  7. Emmons CW, Binford CH, Utz JP, Kwon-Chung KJ. Medical mycology. 3rd ed. Philadelphia: Lea & Febiget 1977: 472.

    Google Scholar 

  8. Fiske RA, Choyce PD, Whitford HW, Martin EC. Phaeohyphomycotic encephalitis in two dogs. J Am Animal Hosp Assoc 1986; 22:237–330.

    Google Scholar 

  9. Iwatsu T. A new species of Cladosporium from Japan. Mycotaxon 1984; 20:521–533.

    Google Scholar 

  10. Jang SS, Biberstein EL, Rinaldi MG, Henness AM, Boorman GA, Taylor RF. Feline brain abscess due to Cladosporium trichoides. Sabouraudia 1977; 15:115–123.

    Google Scholar 

  11. Klite PB, Kelley HB, Dierks FN. A new soil sampling technique for pathogenic fungi. Am J Clin Epidemiol 1965; 31:124–130.

    Google Scholar 

  12. Mandal A, Mohapatra LN. Experimental cladosporiosis. I. Artificial respiratory infection. Indian J Microbiol 1973; 12:205–208.

    Google Scholar 

  13. McGinnis MR. Chromoblastomycosis and phaeohyphomycosis: New concepts, diagnosis, and mycology. Amer Acad Dermatol St. Louis 1983; 8:1–16.

    Google Scholar 

  14. McGinnis MR, Borelli D, Padhye AA, Ajello L. Reclassification of Cladosporium bantianum in the genus Xylohypha. J Clin Microbiol 1986; 23:1148–1151.

    Google Scholar 

  15. Merkow L, Pardo M, Epstein SM, Verney E, Sidransky H. Lysosomal stability during phagocytosis of Aspergillus flavus spores by alveolar macrophages of cortisone-treated mice. Science 1978; 160:79–81.

    Google Scholar 

  16. Newsholme SJ, Tyrer MJ. Cerebral mycosis in a dog caused by Cladosporium trichoides Emmons 1952. Onderstepoort J Vet Research 1980; 47:47–49.

    Google Scholar 

  17. Nishimura K, Miyaji M. Cladosporium trichoides and its parasitic forms in congenitally athymic nude mice and their heterozygous littermates. Mycopathologia 1985; 90:21–28.

    Google Scholar 

  18. Piggott W, Emmons CW. Device for inhalation exposure of animals to spores. Proc Soc Exp Biol Med 103:805–806.

  19. Reed C, Fox JG, Campbell LH. Leukaemia in a cat with concurrent Cladosporium infection. J Small Animal Practice 1974; 15:55–62.

    Google Scholar 

  20. Richard JL, Thurston JR. Rapid hematogenous dissemination of Aspergillus fumigatus and A. flavus spores in turkey poults following aerosol exposure. 1983; 29:1025–1033.

    Google Scholar 

  21. Rogers P, Matossian-Rogers A. Differential sensitivity of lymphocyte subsets to corticosteroid treatment. Immunology 1982; 46:841–848.

    Google Scholar 

  22. Rowatt JD, Hill JO, Lundgren DL. Respiratory infection of cyclosphosphamide-treated mice with Pseudomonas aeruginosa. Exp Lung Res 1983; 5:305–316.

    Google Scholar 

  23. Saito Y, Tsuchiya T, Nomura Y, Takenaka M, Tabuchi K. Three cases of mycosis in Amazona aestiva. Bulletin Azuba Vet College 1967; 1:47–53.

    Google Scholar 

  24. Schaffner A. Therapeutic concentrations of glucocorticoids suppress the antimicrobial activity of human macrophages without impairing their responsiveness to gamma-interferon. J Clin Invest 1985; 76:1755–1764.

    Google Scholar 

  25. Schaffner A, Davis CE, Schaffner T, Markert M, Douglas H, Braude AI. In vitro susceptibility of fungi to killing by neutrophil granulocytes discriminates between primary pathogenecity and opportunism. J Clin Invest 1986; 78:511–524.

    Google Scholar 

  26. Schaffner A, Douglas H, Braude A. Selective protection against conidia by macrophages and against mycelia by polymorphonuclear phagocytes in resistance to Aspergillus. J Clin Invest 1982; 69:619–631.

    Google Scholar 

  27. Shinwari MW, Thomas AD, Orr JD. Feline cerebral phaeohyphomycosis associated with Cladosporium bantianum. Australian Vet J 1985; 62:383–384.

    Google Scholar 

  28. Van Dijk H, Bloksma N, Rademaker PM, Schouten WJ, Willers JM. Differential potencies of corticosterone and hydrocortisone in immune and immune-related processes in the mouse. Internat J Immunopharmacol 1979; 1:285–292.

    Google Scholar 

  29. Walsh TJ, Dixon DM, Polak A, Salkin I. Comparative histopathology of Dactylaria constricta, Fonsecaea pedrosoi, Wangiella dermatitidis, and Xylohypha bantiana in experimental phaeohyphomycosis of the central nervous system. Mykosen 1987; 30:215–225.

    Google Scholar 

  30. Walsh TJ, McEntee C, Dixon DM. Tissue homogenization for quantitative cultures of Candida albicans using sterile reinforced polyethylene bags. J Clin Microbiol 1987; 25: 931–932.

    Google Scholar 

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Dixon, D.M., Merz, W.G., Elliott, H.L. et al. Experimental central nervous system phaeohyphomycosis following intranasal inoculation of Xylohypha bantiana in cortisone-treated mice. Mycopathologia 100, 145–153 (1987). https://doi.org/10.1007/BF00437040

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