{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T12:55:44Z","timestamp":1789563344293,"version":"build-2803163510"},"reference-count":40,"publisher":"PeerJ","license":[{"start":{"date-parts":[[2018,7,27]],"date-time":"2018-07-27T00:00:00Z","timestamp":1532649600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Holsworth Wildlife Research Endowment award"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      The globally distributed epidermal ectoparasite,\n                      <jats:italic>Sarcoptes scabiei,<\/jats:italic>\n                      is a serious health and welfare burden to at-risk human and animal populations. Rapid and sensitive detection of\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      infestation is critical for intervention strategies. While direct microscopy of skin scrapings is a widely utilised diagnostic method, it has low sensitivity. PCR, alternatively, has been shown to readily detect mite DNA even in microscopy-negative skin scrapings. However, a limitation to the latter method is the requirements for specialised equipment and reagents. Such resources may not be readily available in regional or remote clinical settings and are an important consideration in diagnosis of this parasitic disease.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methodology<\/jats:title>\n                    <jats:p>\n                      A Loop Mediated Isothermal Amplification (LAMP) assay targeting the ITS-2 gene for\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      was developed and evaluated on clinical samples from various hosts, previously screened with conventional\n                      <jats:italic>S. scabies<\/jats:italic>\n                      -specific PCR. Species specificity of the newly developed LAMP assay was tested against a range of DNA samples from other arthropods. The LAMP assays were performed on a real-time fluorometer as well as thermal cycler to evaluate an end-point of detection. Using skin scrapings, a rapid sample processing method was assessed to eliminate extensive processing times involved with DNA extractions prior to diagnostic assays, including LAMP.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      LAMP assay was demonstrated to be species-specific and able to detect DNA extracted from a single mite within a skin scraping in under 30 minutes. Application of this assay to DNA extracts from skin scrapings taken from a range of hosts revealed 92.3% congruence (with 92.50% specificity and 100% sensitivity) to the conventional PCR detection of\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      . Preliminary results have indicated that diagnostic outcome from rapidly processed dry skin scrapings using our newly developed LAMP is possible in approximately 40 minutes.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>\n                      We have developed a novel, rapid and robust molecular assay for detecting\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      infesting humans and animals. Based on these findings, we anticipate that this assay will serve an important role as an ancillary diagnostic tool at the point-of-care, complementing existing diagnostic protocols for\n                      <jats:italic>S. scabiei<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.7717\/peerj.5291","type":"journal-article","created":{"date-parts":[[2018,7,27]],"date-time":"2018-07-27T03:55:16Z","timestamp":1532663716000},"page":"e5291","source":"Crossref","is-referenced-by-count":26,"title":["A\n                    <i>Sarcoptes scabiei<\/i>\n                    specific isothermal amplification assay for detection of this important ectoparasite of wombats and other animals"],"prefix":"10.7717","volume":"6","author":[{"given":"Tamieka A.","family":"Fraser","sequence":"first","affiliation":[{"name":"USC Animal Research Centre, Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Sippy 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