{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T12:01:31Z","timestamp":1791892891769,"version":"4.3.4"},"reference-count":43,"publisher":"American Society for Microbiology","issue":"10","license":[{"start":{"date-parts":[[2015,10,1]],"date-time":"2015-10-01T00:00:00Z","timestamp":1443657600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2015,10]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            Appropriate diagnosis and treatment of eumycetoma may vary significantly depending on the causative agent. To date, the most common fungus causing mycetoma worldwide is\n            <jats:named-content content-type=\"genus-species\">Madurella mycetomatis<\/jats:named-content>\n            . This species fails to express any recognizable morphological characteristics, and reliable identification can therefore only be achieved with the application of molecular techniques. Recombinase polymerase amplification (RPA) and loop-mediated isothermal amplification (LAMP) are proposed as alternatives to phenotypic methods. Species-specific primers were developed to target the ribosomal DNA (rDNA) internal transcribed spacer (ITS) region of\n            <jats:named-content content-type=\"genus-species\">M. mycetomatis<\/jats:named-content>\n            . Both isothermal amplification techniques showed high specificity and sufficient sensitivity to amplify fungal DNA and proved to be appropriate for detection of\n            <jats:named-content content-type=\"genus-species\">M. mycetomatis<\/jats:named-content>\n            . Diagnostic performance of the techniques was assessed in comparison to conventional PCR using biopsy specimens from eumycetoma patients. RPA is reliable and easy to operate and has the potential to be implemented in areas where mycetoma is endemic. The techniques may be expanded to detect fungal DNA from environmental samples.\n          <\/jats:p>","DOI":"10.1128\/jcm.01544-15","type":"journal-article","created":{"date-parts":[[2015,8,6]],"date-time":"2015-08-06T02:19:23Z","timestamp":1438827563000},"page":"3280-3285","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":51,"title":["Application of Isothermal Amplification Techniques for Identification of Madurella mycetomatis, the Prevalent Agent of Human Mycetoma"],"prefix":"10.1128","volume":"53","author":[{"given":"Sarah A.","family":"Ahmed","sequence":"first","affiliation":[{"name":"Faculty of Medical Laboratory Sciences, University of Khartoum, Khartoum, Sudan"},{"name":"CBS-KNAW Fungal Biodiversity Centre, Utrecht, Netherlands"},{"name":"Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wendy W. 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