Development of a real-time quantitative PCR assay for detection and quantification of the marine bacterium Alteromonas macleodii from coastal environments

dc.contributor.authorGautam, Pratima
dc.contributor.authorCusick, Kathleen
dc.date.accessioned2023-01-06T18:59:30Z
dc.date.available2023-01-06T18:59:30Z
dc.date.issued2022-12-08
dc.description.abstractAlteromonas macleodii is a ubiquitous marine bacterial species found in a variety of habitats that displays both planktonic and particle-associated lifestyles. Transcriptomic studies demonstrate that, even when present at low abundance, it can make significant contributions to biogeochemical cycles, and its specific association with key marine phytoplankton species indicates other ecological roles as well. It has also been shown to be one of the early colonizers of copper-treated marine vessels. There currently exist no rapid, reliable molecular assays for the detection and quantification of A. macleodii from its different environments. We developed a real-time PCR assay, specific to A. macleodii. This assay targets the DNA gyrase B subunit (gyrB) gene, which occurs as a single copy in the genome. The assay possesses an amplification efficiency of 94.3%, with a limit of detection of 2.5 gyrB copies per μL. Assay specificity was validated by melt curve analysis, followed by sequencing of the amplified product. The assay was specific to thirteen A. macleodii strains and did not amplify other marine bacteria, including Roseobacter denitrificans, Silicibacter sp. TM1040, Vibrio coralliilyticus, Vibrio harveyi, and Vibrio alginolyticus. It also did not amplify Alteromonas mediterranea, a close relative that can occur in the same environment as A. macleodii. This assay was used to determine the presence and abundance of A. macleodii from a range of coastal habitats. The assay was also used to monitor the A. macleodii growth in biofilm and planktonic cultures over time in the presence of elevated copper. This assay provides a rapid and reliable means to assess the presence and abundance of a ubiquitous marine bacterium that, even at low abundance, has been shown to make significant contributions to key marine processes.en_US
dc.description.sponsorshipThis work was supported by UMBC internal funding for KDC.en_US
dc.description.urihttps://www.sciencedirect.com/science/article/pii/S016770122200224X?via%3Dihuben_US
dc.format.extent35 pagesen_US
dc.genrejournal articlesen_US
dc.genrepostprintsen_US
dc.identifierdoi:10.13016/m2mwtk-eung
dc.identifier.citation"Gautam, Pratima and Kathleen D.Cusick. Development of a real-time quantitative PCR assay for detection and quantification of the marine bacterium Alteromonas macleodii from coastal environments. Journal of Microbiological Methods 204, no. 106629 (January 20230). https://doi.org/10.1016/j.mimet.2022.106629"en_US
dc.identifier.urihttps://doi.org/10.1016/j.mimet.2022.106629
dc.identifier.urihttp://hdl.handle.net/11603/26585
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Biological Sciences Department Collection
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Student Collection
dc.rightsThis 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.rightsAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)*
dc.rightsAccess to this item will begin on 01/31/2024
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleDevelopment of a real-time quantitative PCR assay for detection and quantification of the marine bacterium Alteromonas macleodii from coastal environmentsen_US
dc.typeTexten_US
dcterms.creatorhttps://orcid.org/0000-0001-7224-3472en_US

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