In Vivo Analysis of Aspergillus fumigatus Developmental Gene Expression Determined by Real-Time Reverse Transcription-PCR
Very little is known about the developmental stages of Aspergillus fumigatus during invasive aspergillosis. We performed real-time reverse transcription-PCR analysis on lung samples from mice with invasive pulmonary aspergillosis to determine the expression of A. fumigatus genes that are expressed a...
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Veröffentlicht in: | Infection and Immunity 2008-08, Vol.76 (8), p.3632-3639 |
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description | Very little is known about the developmental stages of Aspergillus fumigatus during invasive aspergillosis. We performed real-time reverse transcription-PCR analysis on lung samples from mice with invasive pulmonary aspergillosis to determine the expression of A. fumigatus genes that are expressed at specific stages of development. In established infection, A. fumigatus exhibited mRNA expression of genes specific to developmentally competent hyphae, such as stuA. In contrast, mRNA of genes expressed by conidia and precompetent hyphae was not detected. Many genes required for mycotoxin synthesis, including aspHS, gliP, mitF, and metAP, are known to be expressed by developmentally competent hyphae in vitro. Interestingly, each of these genes was expressed at significantly higher levels during invasive infection than in vitro. The expression of gliP mRNA in vitro was found to be highly dependent on culture conditions. Furthermore, gliP expression was found to be dependent on the transcription factor StuA both in vitro and in vivo. Therefore, developmentally competent hyphae predominate during established invasive infection, and many mycotoxin genes are expressed at high levels in vivo. These results highlight the importance of the evaluation of putative virulence factors expressed by competent hyphae and analysis of gene expression levels during invasive infection rather than in vitro alone. |
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We performed real-time reverse transcription-PCR analysis on lung samples from mice with invasive pulmonary aspergillosis to determine the expression of A. fumigatus genes that are expressed at specific stages of development. In established infection, A. fumigatus exhibited mRNA expression of genes specific to developmentally competent hyphae, such as stuA. In contrast, mRNA of genes expressed by conidia and precompetent hyphae was not detected. Many genes required for mycotoxin synthesis, including aspHS, gliP, mitF, and metAP, are known to be expressed by developmentally competent hyphae in vitro. Interestingly, each of these genes was expressed at significantly higher levels during invasive infection than in vitro. The expression of gliP mRNA in vitro was found to be highly dependent on culture conditions. Furthermore, gliP expression was found to be dependent on the transcription factor StuA both in vitro and in vivo. Therefore, developmentally competent hyphae predominate during established invasive infection, and many mycotoxin genes are expressed at high levels in vivo. These results highlight the importance of the evaluation of putative virulence factors expressed by competent hyphae and analysis of gene expression levels during invasive infection rather than in vitro alone.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.01483-07</identifier><identifier>PMID: 18490465</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Aspergillosis - microbiology ; Aspergillus fumigatus ; Aspergillus fumigatus - genetics ; Aspergillus fumigatus - physiology ; Biological and medical sciences ; Fundamental and applied biological sciences. 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We performed real-time reverse transcription-PCR analysis on lung samples from mice with invasive pulmonary aspergillosis to determine the expression of A. fumigatus genes that are expressed at specific stages of development. In established infection, A. fumigatus exhibited mRNA expression of genes specific to developmentally competent hyphae, such as stuA. In contrast, mRNA of genes expressed by conidia and precompetent hyphae was not detected. Many genes required for mycotoxin synthesis, including aspHS, gliP, mitF, and metAP, are known to be expressed by developmentally competent hyphae in vitro. Interestingly, each of these genes was expressed at significantly higher levels during invasive infection than in vitro. The expression of gliP mRNA in vitro was found to be highly dependent on culture conditions. Furthermore, gliP expression was found to be dependent on the transcription factor StuA both in vitro and in vivo. Therefore, developmentally competent hyphae predominate during established invasive infection, and many mycotoxin genes are expressed at high levels in vivo. These results highlight the importance of the evaluation of putative virulence factors expressed by competent hyphae and analysis of gene expression levels during invasive infection rather than in vitro alone.</description><subject>Animals</subject><subject>Aspergillosis - microbiology</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - genetics</subject><subject>Aspergillus fumigatus - physiology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal and Parasitic Infections</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Hyphae - genetics</subject><subject>Lung - microbiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Mycology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>Spores, Fungal - genetics</subject><subject>Virulence Factors - biosynthesis</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0U9v0zAcBuAIgVgZ3DhDOMCJDNvxn-SCVJUxKk0CjY6r5Tg_p0ZOnNlJod8eb60GnOBkO3702s6bZc8xOsOYVO_Wy_UZwrQqCyQeZAuM6qpgjJCH2QIhXBc14-IkexLj97SklFaPsxNc0RpRzhbZfj3k3-zO58tBuX20MfcmX8YRQmedm2Nu5t52akqzD7AD58cehkm5_AIGyM9_jgFitH5IuxOE3g7Q5s0-vwLlio3tIc12ECLkm6CGqIMdp6SLL6urp9kjo1yEZ8fxNLv-eL5ZfSouP1-sV8vLQjNCp6IktDak1MpQILzGiDbaYMO5brnATSs0VYwzLBrVtgk3NRUNAya0wpC-lqfZ-0PuODc9tDpdPygnx2B7FfbSKyv_3hnsVnZ-J9PBKa9MAW-OAcHfzBAn2duowTk1gJ-j5IlVJWP_hAQzhATC_wERIVjcwrcHqIOPMYC5vzZG8rZ9mdqXd-1LJBJ_8edTf-Nj3Qm8PgIVtXImdaJtvHcEMVqxkiT36uC2ttv-sAGkir206VcJLitZ8jvz8mCM8lJ1IeVcfyXpdQjVmBNBy1-1VM2v</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Gravelat, Fabrice N</creator><creator>Doedt, Thomas</creator><creator>Chiang, Lisa Y</creator><creator>Liu, Hong</creator><creator>Filler, Scott G</creator><creator>Patterson, Thomas F</creator><creator>Sheppard, Donald C</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><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>7QO</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080801</creationdate><title>In Vivo Analysis of Aspergillus fumigatus Developmental Gene Expression Determined by Real-Time Reverse Transcription-PCR</title><author>Gravelat, Fabrice N ; Doedt, Thomas ; Chiang, Lisa Y ; Liu, Hong ; Filler, Scott G ; Patterson, Thomas F ; Sheppard, Donald C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-3249f23caf4e269104bcf1f66cd671bd7c4a56517badd324b947b5e57ca1e17b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Aspergillosis - microbiology</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - genetics</topic><topic>Aspergillus fumigatus - physiology</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal and Parasitic Infections</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Fungal</topic><topic>Hyphae - genetics</topic><topic>Lung - microbiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mycology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>Spores, Fungal - genetics</topic><topic>Virulence Factors - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gravelat, Fabrice N</creatorcontrib><creatorcontrib>Doedt, Thomas</creatorcontrib><creatorcontrib>Chiang, Lisa Y</creatorcontrib><creatorcontrib>Liu, Hong</creatorcontrib><creatorcontrib>Filler, Scott G</creatorcontrib><creatorcontrib>Patterson, Thomas F</creatorcontrib><creatorcontrib>Sheppard, Donald C</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gravelat, Fabrice N</au><au>Doedt, Thomas</au><au>Chiang, Lisa Y</au><au>Liu, Hong</au><au>Filler, Scott G</au><au>Patterson, Thomas F</au><au>Sheppard, Donald C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vivo Analysis of Aspergillus fumigatus Developmental Gene Expression Determined by Real-Time Reverse Transcription-PCR</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>76</volume><issue>8</issue><spage>3632</spage><epage>3639</epage><pages>3632-3639</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Very little is known about the developmental stages of Aspergillus fumigatus during invasive aspergillosis. We performed real-time reverse transcription-PCR analysis on lung samples from mice with invasive pulmonary aspergillosis to determine the expression of A. fumigatus genes that are expressed at specific stages of development. In established infection, A. fumigatus exhibited mRNA expression of genes specific to developmentally competent hyphae, such as stuA. In contrast, mRNA of genes expressed by conidia and precompetent hyphae was not detected. Many genes required for mycotoxin synthesis, including aspHS, gliP, mitF, and metAP, are known to be expressed by developmentally competent hyphae in vitro. Interestingly, each of these genes was expressed at significantly higher levels during invasive infection than in vitro. The expression of gliP mRNA in vitro was found to be highly dependent on culture conditions. Furthermore, gliP expression was found to be dependent on the transcription factor StuA both in vitro and in vivo. Therefore, developmentally competent hyphae predominate during established invasive infection, and many mycotoxin genes are expressed at high levels in vivo. These results highlight the importance of the evaluation of putative virulence factors expressed by competent hyphae and analysis of gene expression levels during invasive infection rather than in vitro alone.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>18490465</pmid><doi>10.1128/IAI.01483-07</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Aspergillosis - microbiology Aspergillus fumigatus Aspergillus fumigatus - genetics Aspergillus fumigatus - physiology Biological and medical sciences Fundamental and applied biological sciences. Psychology Fungal and Parasitic Infections Gene Expression Profiling Gene Expression Regulation, Fungal Hyphae - genetics Lung - microbiology Male Mice Mice, Inbred BALB C Microbiology Miscellaneous Mycology Reverse Transcriptase Polymerase Chain Reaction - methods Spores, Fungal - genetics Virulence Factors - biosynthesis |
title | In Vivo Analysis of Aspergillus fumigatus Developmental Gene Expression Determined by Real-Time Reverse Transcription-PCR |
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