impaginato piccolo - Società Italiana di Parassitologia (SoIPa)
impaginato piccolo - Società Italiana di Parassitologia (SoIPa)
impaginato piccolo - Società Italiana di Parassitologia (SoIPa)
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
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 />
Anane S, Anane Touzri R, Malouche N, El Aich F, Beltaief O,<br />
Zhioua R, Kaouech E, Belhaj S, Kallel K, Jed<strong>di</strong> A, Meddeb<br />
Ouertani A, Chaker E (2007). Which is the role of parasites and<br />
yeasts in the genesis of chronic blepharitis? Pathol Biol (Paris)<br />
55: 323-7.<br />
Batra R, Boekhout T, Gueho E, Cabanes FJ, Dawson TL Jr, Gupta<br />
AK (2005). Malassezia Baillon, emerging clinical yeasts. FEMS<br />
Yeast Res 5: 1101-13.<br />
Belew PW, Rosenberg EW, Jennings BR (1980). Activation of the<br />
alternative pathway of complement by Malassezia ovalis<br />
(Pityrosporum ovale). Mycopathologia 70: 187-91.<br />
Bergbrant IM (1995). Seborrhoeic dermatitis and Pityrosporum<br />
yeasts. Curr Top Med Mycol 6: 95-112.<br />
Cafarchia C, Dell’Aquila ME, Capelli G, Minoia P, Otranto D<br />
(2007a). Role of beta-endorphin on phospholipase production<br />
in Malassezia pachydermatis in dogs: new insights into the<br />
pathogenesis of this yeast. Med Mycol 45: 11-5.<br />
Cafarchia C, Gallo S, Capelli G, Otranto D (2005a). Occurrence<br />
and population size of Malassezia spp. in the external ear canal<br />
of dogs and cats both healthy and with otitis. Mycopathologia<br />
160: 143-9.<br />
Cafarchia C, Gallo S, Danesi P, Capelli G, Para<strong>di</strong>es P, Traversa D,<br />
Gasser RB, Otranto D (2008a). Assessing the relationship<br />
between Malassezia and leishmaniasis in dogs with or without<br />
skin lesions. Acta Trop doi:10.1016/j.actatropica.2008.04.008.<br />
Cafarchia C, Gallo S, Dell’Aquila ME, Otranto D (2007b). Effect of<br />
Beta–endorphin and Naloxone in modulating phospholipase<br />
production in Malassezia pachydermatis from dogs. 3rd Trends<br />
in Me<strong>di</strong>cal Mycology 28-31 October, Torino, Italy.<br />
Cafarchia C, Gallo S, Romito D, Capelli G, Chermette R, Guillot J,<br />
Otranto D (2005b). Frequency, body <strong>di</strong>stribution, and population<br />
size of Malassezia species in healthy dogs and in dogs with<br />
localized cutaneous lesions. J Vet Diagn Invest 17: 316-22.<br />
Cafarchia C, Gasser RB, Latrofa MS, Parisi A, Campbell BE,<br />
Otranto D (2008b). Genetic variants of Malassezia pachydermatis<br />
from canine skin: body <strong>di</strong>stribution and phospholipase activity.<br />
FEMS Yeast Res 8(3): 451-9.<br />
Cafarchia C, Latrofa MS, Testini G, Parisi A, Guillot J, Gasser RB,<br />
Otranto D (2007c). Molecular characterization of Malassezia isolates<br />
from dogs using three <strong>di</strong>stinct genetic markers in nuclear<br />
DNA. Mol Cell Probes 21: 229-38.<br />
Cafarchia C, Otranto D (2004). Association between phospholipase<br />
production by Malassezia pachydermatis and skin lesions.<br />
J Clin Microbiol 42: 4868-9.<br />
Cafarchia C, Otranto D, Campbell BE, Latrofa MS, Guillot J,<br />
Gasser RB (2007d). Multilocus mutation scanning for the analysis<br />
of genetic variation within Malassezia (Basi<strong>di</strong>omycota:<br />
Malasseziales). Electrophoresis 28: 1176-80.<br />
Chen TA, Hill PB (2005). The biology of Malassezia organisms and<br />
their ability to induce immune responses and skin <strong>di</strong>sease. Vet<br />
Dermatol 16: 4-26.<br />
Coutinho SD, Paula CR (2000). Proteinase, phospholipase,<br />
hyaluronidase and chondroitin-sulphatase production by<br />
Malassezia pachydermatis. Med Mycol 38: 73-6.<br />
Guillot J, Bond R (1999). Malassezia pachydermatis: a review.