<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>37(8)</volume><submitter>Hue FX</submitter><pubmed_abstract>Fusarium species are opportunistic nosocomial pathogens that often cause fatal invasive mycoses. We designed a primer pair that amplifies by PCR a fragment of a gene coding for the rRNA of Fusarium species. The DNAs of the main Fusarium species and Neocosmospora vasinfecta but not the DNAs from 11 medically important fungi were amplified by these primers. The lower limit of detection of the PCR system was 10 fg of Fusarium solani DNA by ethidium bromide staining. To test the ability of this PCR system to detect Fusarium DNA in tissues, we developed a mouse model of disseminated fusariosis. Using the PCR, we detected Fusarium DNA in mouse tissues and in spiked human blood. Furthermore, F. solani, Fusarium moniliforme, and Fusarium oxysporum were testing by random amplified polymorphic DNA (</pubmed_abstract><journal>Journal of clinical microbiology</journal><pagination>2434-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC85247</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Specific detection of fusarium species in blood and tissues by a PCR technique.</pubmed_title><pmcid>PMC85247</pmcid><pubmed_authors>Hue FX</pubmed_authors><pubmed_authors>Rouffault MA</pubmed_authors><pubmed_authors>Huerre M</pubmed_authors><pubmed_authors>de Bievre C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Specific detection of fusarium species in blood and tissues by a PCR technique.</name><description>Fusarium species are opportunistic nosocomial pathogens that often cause fatal invasive mycoses. We designed a primer pair that amplifies by PCR a fragment of a gene coding for the rRNA of Fusarium species. The DNAs of the main Fusarium species and Neocosmospora vasinfecta but not the DNAs from 11 medically important fungi were amplified by these primers. The lower limit of detection of the PCR system was 10 fg of Fusarium solani DNA by ethidium bromide staining. To test the ability of this PCR system to detect Fusarium DNA in tissues, we developed a mouse model of disseminated fusariosis. Using the PCR, we detected Fusarium DNA in mouse tissues and in spiked human blood. Furthermore, F. solani, Fusarium moniliforme, and Fusarium oxysporum were testing by random amplified polymorphic DNA (</description><dates><release>1999-01-01T00:00:00Z</release><publication>1999 Aug</publication><modification>2025-05-29T19:24:48.82Z</modification><creation>2019-03-27T00:18:19Z</creation></dates><accession>S-EPMC85247</accession><cross_references><pubmed>10405380</pubmed><doi>10.1128/JCM.37.8.2434-2438.1999</doi></cross_references></HashMap>