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Real-Time PCR Identification of Six Malassezia Species
Lipophilic yeast Malassezia species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor, Malassezia folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of Malassezia with conventional methods. We...
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Published in: | Current microbiology 2017-06, Vol.74 (6), p.671-677 |
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creator | Ilahi, Amin Hadrich, Inès Neji, Sourour Trabelsi, Houaida Makni, Fattouma Ayadi, Ali |
description | Lipophilic yeast
Malassezia
species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor,
Malassezia
folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of
Malassezia
with conventional methods. We developed a real-time polymerase chain reaction (PCR) assay with multiple hybridization probes for detecting
M. globosa, M. furfur, M. restricta, M. sympodialis, M. slooffiae
, and
M. pachydermatis
. The amplification curves and specific melting peaks of the probes hybridized with real-time PCR product were used for species identifications. The assay was further evaluated on 120 samples which were performed by swabbing from 60 domestic animals (23 goats, 10 dogs, 15 cows, 3 cats, 8 rabbits, and 1 donkey) and in 70 human samples (28 patients with pityriasis versicolor, 17 breeders, and 25 control group). Fifteen
M. pachydermatis
were identified from animals. From human, 61 isolates were identified as
M. globosa
(28),
M. furfur
(15),
M. restricta
(6),
M. sympodialis
(8),
M. slooffiae
(2), and
M. pachydermatis
(2). Eight cases of co-detection from 6 patients and 2 breeders were revealed. Our findings show that the assay was highly effective in identifying
Malassezia
species. The application of multiplex real-time PCR provides a sensitive and rapid identification system for Malassezia species, which may be applied in further epidemiological surveys from clinical samples. |
doi_str_mv | 10.1007/s00284-017-1237-7 |
format | article |
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Malassezia
species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor,
Malassezia
folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of
Malassezia
with conventional methods. We developed a real-time polymerase chain reaction (PCR) assay with multiple hybridization probes for detecting
M. globosa, M. furfur, M. restricta, M. sympodialis, M. slooffiae
, and
M. pachydermatis
. The amplification curves and specific melting peaks of the probes hybridized with real-time PCR product were used for species identifications. The assay was further evaluated on 120 samples which were performed by swabbing from 60 domestic animals (23 goats, 10 dogs, 15 cows, 3 cats, 8 rabbits, and 1 donkey) and in 70 human samples (28 patients with pityriasis versicolor, 17 breeders, and 25 control group). Fifteen
M. pachydermatis
were identified from animals. From human, 61 isolates were identified as
M. globosa
(28),
M. furfur
(15),
M. restricta
(6),
M. sympodialis
(8),
M. slooffiae
(2), and
M. pachydermatis
(2). Eight cases of co-detection from 6 patients and 2 breeders were revealed. Our findings show that the assay was highly effective in identifying
Malassezia
species. The application of multiplex real-time PCR provides a sensitive and rapid identification system for Malassezia species, which may be applied in further epidemiological surveys from clinical samples.</description><identifier>ISSN: 0343-8651</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-017-1237-7</identifier><identifier>PMID: 28332161</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animals ; Biomedical and Life Sciences ; Biotechnology ; Cats ; Cattle - microbiology ; Dermatitis ; Dogs ; Domestic animals ; Equidae - microbiology ; Fungi ; Goats - microbiology ; Humans ; Life Sciences ; Malassezia ; Malassezia - classification ; Malassezia - genetics ; Malassezia - isolation & purification ; Microbiology ; Molecular Typing - methods ; Mycological Typing Techniques - methods ; Nucleic Acid Denaturation - genetics ; Polymerase chain reaction ; Probes ; Rabbits ; Real-Time Polymerase Chain Reaction - methods ; RNA, Ribosomal - genetics ; Skin - microbiology ; Skin diseases ; Tinea Versicolor - microbiology ; Yeast ; Yeasts</subject><ispartof>Current microbiology, 2017-06, Vol.74 (6), p.671-677</ispartof><rights>Springer Science+Business Media New York 2017</rights><rights>Current Microbiology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-29cc785eadcb8aab19c0acd3152bfae6980c9d13950b506a1c0eeead977513553</citedby><cites>FETCH-LOGICAL-c405t-29cc785eadcb8aab19c0acd3152bfae6980c9d13950b506a1c0eeead977513553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28332161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ilahi, Amin</creatorcontrib><creatorcontrib>Hadrich, Inès</creatorcontrib><creatorcontrib>Neji, Sourour</creatorcontrib><creatorcontrib>Trabelsi, Houaida</creatorcontrib><creatorcontrib>Makni, Fattouma</creatorcontrib><creatorcontrib>Ayadi, Ali</creatorcontrib><title>Real-Time PCR Identification of Six Malassezia Species</title><title>Current microbiology</title><addtitle>Curr Microbiol</addtitle><addtitle>Curr Microbiol</addtitle><description>Lipophilic yeast
Malassezia
species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor,
Malassezia
folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of
Malassezia
with conventional methods. We developed a real-time polymerase chain reaction (PCR) assay with multiple hybridization probes for detecting
M. globosa, M. furfur, M. restricta, M. sympodialis, M. slooffiae
, and
M. pachydermatis
. The amplification curves and specific melting peaks of the probes hybridized with real-time PCR product were used for species identifications. The assay was further evaluated on 120 samples which were performed by swabbing from 60 domestic animals (23 goats, 10 dogs, 15 cows, 3 cats, 8 rabbits, and 1 donkey) and in 70 human samples (28 patients with pityriasis versicolor, 17 breeders, and 25 control group). Fifteen
M. pachydermatis
were identified from animals. From human, 61 isolates were identified as
M. globosa
(28),
M. furfur
(15),
M. restricta
(6),
M. sympodialis
(8),
M. slooffiae
(2), and
M. pachydermatis
(2). Eight cases of co-detection from 6 patients and 2 breeders were revealed. Our findings show that the assay was highly effective in identifying
Malassezia
species. The application of multiplex real-time PCR provides a sensitive and rapid identification system for Malassezia species, which may be applied in further epidemiological surveys from clinical samples.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Cats</subject><subject>Cattle - microbiology</subject><subject>Dermatitis</subject><subject>Dogs</subject><subject>Domestic animals</subject><subject>Equidae - microbiology</subject><subject>Fungi</subject><subject>Goats - microbiology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Malassezia</subject><subject>Malassezia - classification</subject><subject>Malassezia - genetics</subject><subject>Malassezia - isolation & purification</subject><subject>Microbiology</subject><subject>Molecular Typing - methods</subject><subject>Mycological Typing Techniques - methods</subject><subject>Nucleic Acid Denaturation - genetics</subject><subject>Polymerase chain reaction</subject><subject>Probes</subject><subject>Rabbits</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>RNA, Ribosomal - genetics</subject><subject>Skin - microbiology</subject><subject>Skin diseases</subject><subject>Tinea Versicolor - microbiology</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0343-8651</issn><issn>1432-0991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkMFqGzEQhkVJaBy3D9BLWMilFzUz0molHYNJmoBLiu2ehVY7GxTWu87KhrRPXxknpQQCOc1hvv8f5mPsC8I3BNAXCUCYkgNqjkJqrj-wCZZScLAWj9gEZCm5qRSesNOUHgBQWMCP7EQYKQVWOGHVgnzHV3FNxc_ZorhtqN_GNga_jUNfDG2xjE_FD9_5lOhP9MVyQyFS-sSOW98l-vw8p-zX9dVqdsPnd99vZ5dzHkpQWy5sCNoo8k2ojfc12gA-NBKVqFtPlTUQbIPSKqgVVB4DEGXaaq1QKiWn7OuhdzMOjztKW7eOKVDX-Z6GXXJorJYGDcA7UANlvmjKjJ6_Qh-G3djnR_aFKEVphMwUHqgwDimN1LrNGNd-_O0Q3N6_O_h32b_b-3c6Z86em3f1mpp_iRfhGRAHIOVVf0_jf6ffbP0L84CNSA</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Ilahi, Amin</creator><creator>Hadrich, Inès</creator><creator>Neji, Sourour</creator><creator>Trabelsi, Houaida</creator><creator>Makni, Fattouma</creator><creator>Ayadi, Ali</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>Real-Time PCR Identification of Six Malassezia Species</title><author>Ilahi, Amin ; Hadrich, Inès ; Neji, Sourour ; Trabelsi, Houaida ; Makni, Fattouma ; Ayadi, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-29cc785eadcb8aab19c0acd3152bfae6980c9d13950b506a1c0eeead977513553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cats</topic><topic>Cattle - 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Academic</collection><jtitle>Current microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ilahi, Amin</au><au>Hadrich, Inès</au><au>Neji, Sourour</au><au>Trabelsi, Houaida</au><au>Makni, Fattouma</au><au>Ayadi, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-Time PCR Identification of Six Malassezia Species</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><addtitle>Curr Microbiol</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>74</volume><issue>6</issue><spage>671</spage><epage>677</epage><pages>671-677</pages><issn>0343-8651</issn><eissn>1432-0991</eissn><abstract>Lipophilic yeast
Malassezia
species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor,
Malassezia
folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of
Malassezia
with conventional methods. We developed a real-time polymerase chain reaction (PCR) assay with multiple hybridization probes for detecting
M. globosa, M. furfur, M. restricta, M. sympodialis, M. slooffiae
, and
M. pachydermatis
. The amplification curves and specific melting peaks of the probes hybridized with real-time PCR product were used for species identifications. The assay was further evaluated on 120 samples which were performed by swabbing from 60 domestic animals (23 goats, 10 dogs, 15 cows, 3 cats, 8 rabbits, and 1 donkey) and in 70 human samples (28 patients with pityriasis versicolor, 17 breeders, and 25 control group). Fifteen
M. pachydermatis
were identified from animals. From human, 61 isolates were identified as
M. globosa
(28),
M. furfur
(15),
M. restricta
(6),
M. sympodialis
(8),
M. slooffiae
(2), and
M. pachydermatis
(2). Eight cases of co-detection from 6 patients and 2 breeders were revealed. Our findings show that the assay was highly effective in identifying
Malassezia
species. The application of multiplex real-time PCR provides a sensitive and rapid identification system for Malassezia species, which may be applied in further epidemiological surveys from clinical samples.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28332161</pmid><doi>10.1007/s00284-017-1237-7</doi><tpages>7</tpages></addata></record> |
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source | Springer Nature |
subjects | Animals Biomedical and Life Sciences Biotechnology Cats Cattle - microbiology Dermatitis Dogs Domestic animals Equidae - microbiology Fungi Goats - microbiology Humans Life Sciences Malassezia Malassezia - classification Malassezia - genetics Malassezia - isolation & purification Microbiology Molecular Typing - methods Mycological Typing Techniques - methods Nucleic Acid Denaturation - genetics Polymerase chain reaction Probes Rabbits Real-Time Polymerase Chain Reaction - methods RNA, Ribosomal - genetics Skin - microbiology Skin diseases Tinea Versicolor - microbiology Yeast Yeasts |
title | Real-Time PCR Identification of Six Malassezia Species |
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