Rapid sample preparation with Lyse-It® for Listeria monocytogenes and Vibrio cholerae
| dc.contributor.author | Santaus, Tonya | |
| dc.contributor.author | Li, Shan | |
| dc.contributor.author | Ladd, Paula | |
| dc.contributor.author | Harvey, Amanda | |
| dc.contributor.author | Cole, Shannon | |
| dc.contributor.author | Stine, O. Colin | |
| dc.contributor.author | Geddes, Chris | |
| dc.date.accessioned | 2023-07-27T21:08:24Z | |
| dc.date.available | 2023-07-27T21:08:24Z | |
| dc.date.issued | 2018-07-25 | |
| dc.description.abstract | Sample preparation is a leading bottleneck in rapid detection of pathogenic bacteria. Here, we use Lyse-It® for bacterial cellular lysis, genomic DNA fragmentation, and protein release and degradation for both Listeria monocytogenes and Vibrio cholerae. The concept of Lyse-It® employs a conventional microwave and Lyse-It® slides for intensely focused microwave irradiation onto the sample. High microwave power and a <60 second irradiation time allow for rapid cellular lysis and subsequent intracellular component release. The pathogenic bacteria are identified by quantitative polymerase chain reaction (qPCR), which subsequently demonstrates the viability of DNA for amplification post microwave-induced lysis. Intracellular component release, degradation, and detection of L. monocytogenes and V. cholerae has been performed and shown in this paper. These results demonstrate a rapid, low-cost, and efficient way for bacterial sample preparation on both food and water-borne Gram-positive and -negative organisms alike. | en_US |
| dc.description.sponsorship | This work is supported by the UMBCUMB Cholera joint training grant and the National Institutes of Health UMBC Graduate Training Chemistry Biology Interface Fellowship (T32GM066706-14). We would also like to thank the Institute of Fluorescence and the University of Maryland School Medicine departments of Public Health and Epidemiology for their support, advice, and funding. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. | en_US |
| dc.description.uri | https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0201070 | en_US |
| dc.format.extent | 14 pages | en_US |
| dc.genre | journal articles | en_US |
| dc.identifier | doi:10.13016/m2lupw-taar | |
| dc.identifier.citation | Santaus TM, Li S, Ladd P, Harvey A, Cole S, et al. (2018) Rapid sample preparation with Lyse-It® for Listeria monocytogenes and Vibrio cholerae. PLOS ONE 13(7): e0201070. https://doi.org/10.1371/journal.pone.0201070 | en_US |
| dc.identifier.uri | https://doi.org/10.1371/journal.pone.0201070 | |
| dc.identifier.uri | http://hdl.handle.net/11603/28906 | |
| dc.language.iso | en_US | en_US |
| dc.publisher | PLOS | en_US |
| dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
| dc.relation.ispartof | UMBC Institute of Flourescence | |
| dc.relation.ispartof | UMBC Chemistry & Biochemistry Department | |
| dc.relation.ispartof | UMBC Faculty Collection | |
| dc.relation.ispartof | UMBC Student Collection | |
| dc.rights | This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author. | en_US |
| dc.rights | Attribution 4.0 International (CC BY 4.0) | * |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | * |
| dc.title | Rapid sample preparation with Lyse-It® for Listeria monocytogenes and Vibrio cholerae | en_US |
| dc.type | Text | en_US |
| dcterms.creator | https://orcid.org/0000-0002-8643-2343 | en_US |
| dcterms.creator | https://orcid.org/0000-0003-1805-1407 | en_US |
| dcterms.creator | https://orcid.org/0000-0002-9110-6374 | en_US |
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