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66<br />

C. Cafarchia, D. Otranto - Malassezia spp. as a pathogenic yeasts<br />

(Continuho and Paula, 2000; Mancianti et al, 2001) of<br />

which, the latter, could contribute to pruritus as me<strong>di</strong>ators<br />

of itch (in Chen and Hill, 2005). Lipases, contribute<br />

to produce fatty acids on the skin which can be<br />

used by yeasts for nutrition provi<strong>di</strong>ng protection by<br />

other inhibiting organisms (in Chen and Hill, 2005).<br />

M. pachydermatis also produces phospholipase and a<br />

higher phospholipase activity was found in isolates<br />

from skin lesion than in strains from healthy skin<br />

(Cafarchia and Otranto, 2004). Further stu<strong>di</strong>es demonstrated<br />

that β-endorphin (a class of endogenous opioid<br />

peptides) induces M. pachydermatis cell <strong>di</strong>fferentiation<br />

towards the production or non -production of phospholipase<br />

(Cafarchia et al, 2007a). The presence of muopioid<br />

receptors on the M. pachydermatis cells and the<br />

effect of naloxon (i.e. an opioid antagonist receptor),<br />

on the phospholipase activity has been investigated<br />

(Cafarchia et al, 2007b) and results in<strong>di</strong>cated that mu<br />

opioid receptors are expressed in M. pachydermatis cell<br />

walls. The above results suggested that this receptor<br />

may be involved in me<strong>di</strong>ating the effects of both opioid<br />

agonist (β-endorphin) and antagonist (Naloxon) on<br />

phospholipase production of M. pachydermatis thus<br />

opening new avenues for topical control of Malassezia<br />

lesions.<br />

The host, the Malassezia and the Leishmania infantum<br />

protozoa.<br />

The relationship among the frequency, population size<br />

and phospholipase activity of M. pachydermatis was<br />

investigated for dogs with (Li + ) and without (Li - )<br />

Leishmania infantum infection. A significantly higher<br />

mean population size of M. pachydermatis was cultured<br />

from the skin of L + compared with L - dogs. For<br />

M. pachydermatis, most phospolipase-producing cultures<br />

and the highest phospholipase activity were<br />

recorded for L - dogs with lesions and L + dogs without<br />

lesions. Although M. pachydermatis was a common<br />

commensal on dogs with or without L. infantum infection,<br />

L. infantum infection in dogs without skin lesions<br />

are associated with increased growth of M. pachydermatis<br />

and production of phospholipase in vitro<br />

(Cafarchia et al, 2008a).<br />

Conclusive remarks<br />

The pathogenic role of Malassezia yeasts is related to<br />

changes in the normal physical, chemical or immunological<br />

mechanisms of the skin which may enhance or<br />

down regulate the molecular production of yeast virulence<br />

factors or antigens. As an example the chemical<br />

composition of Malassezia cell wall (i.e. the expression<br />

of mu -opioid receptors) may be strictly related to the<br />

chemical composition of the skin (presence of β-endorphin)<br />

and may play a fundamental role in influencing<br />

the pathogenic or commensal phenotype of Malassezia<br />

yeasts. Without any doubt further stu<strong>di</strong>es and researches<br />

are needed in this field in order to better understand<br />

the complex interactions between Malassezia and host<br />

immune system by investigating genomic and proteomic<br />

aspects of this relationship.<br />

References<br />

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