Molecular Detection of Legionella spp. and their associations with Mycobacterium spp., Pseudomonas aeruginosa and amoeba hosts in a drinking water distribution system
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Quantity of Legionella spp., Mycobacterium spp., Acanthamoeba,Vermamoeba vermiformis and Pseudomonas aeruginosa were estimated using qPCR methods. This dataset is associated with the following publication: Lu , J., I. Struewing, E. Vereen, A.E. Kirby, K. Levy, C. Moe, and N. Ashbolt. Molecular detection of Legionella spp. and their associations with Mycobacterium spp., Pseudomonas aeruginosa and amoeba hosts in a drinking water distribution system (Journal Article). JOURNAL OF APPLIED MICROBIOLOGY. Blackwell Publishing, Malden, MA, USA, 120(2): 509-521, (2016).
Algal toxins and Mycobacterium avium ssp. paratuberculosis measured in surface-water, quarry-water, and sediment samples collected at Pipestone National Monument, Pipestone, Minnesota, 2018-19
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The U.S. Geological Survey, in cooperation with the U.S. National Park Service, conducted a study to determine the presence of algal toxins and Mycobacterium avium ssp. paratuberculosis (MAP) within Pipestone National Monument located in Pipestone County in southwestern Minnesota. Three algal toxins (microcystins, saxitoxin, and anatoxin-a) were analyzed in 12 water-quality samples collected from 8 surface and 2 quarry-water sample sites by enzyme-linked immunosorbent assay (ELISA) methods. Two of the three analyzed algal toxins (microcystins and anatoxin-a) were also analyzed using immunosorbent strip test methods. All analysis kits were provided by Abraxis Inc. (Warminister, Pa) and analyses were completed at the U.S. Geological Survey - Upper Midwest Water Science Center in Mounds View, Minnesota. MAP was analyzed in 16 water-quality samples and 8 sediment samples collected from 8 surface-water sample sites by multiple real-time polymerase chain reaction (PCR) methods at the Wisconsin Veterinary Diagnostic Laboratory at the University of Wisconsin-Madison in Madison, Wisconsin. These data are a part of a larger study and an associated report documented in the U.S. Geological Survey Investigations Report 2023-XXXX (http://doiXXXXXplaceholder).
Hawaii Island airborne detection of fungal pathogens of Ohia, 2016-2017
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This data release includes metadata and tabular datasets that document (1) Austropuccina, Ceratocystis and Myrtaceae qPCR (quantitative polymerase chain reaction) DNA detections in Passive Environmental Samplers (PES), (2) wind speed, wind gust speed, and wind direction measurements collected at two sites in the Kahuku Unit of Hawai'i Volcanoes National Park (HAVO) where paired PES were located, (3) localities, sites and elevations where PES were located, and (4) Genbank accession numbers for Austropuccinia and Ceratocystis DNA sequences amplified from samples collected in a subset of PES. These raw data were analyzed and reported in the manuscript "Environmental Monitoring for Invasive Fungal Pathogens of ʽŌhiʽa (Metrosideros polymorpha) on the Island of Hawaiʽi".
Identification of two
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Background The ability of Mycobacterium tuberculosis to survive and replicate in macrophages is crucial for the mycobacterium's ability to infect the host and cause tuberculosis. To identify Mycobacterium tuberculosis genes involved in survival in macrophages, a library of non-pathogenic Mycobacterium smegmatis bacteria, each carrying an individual integrated cosmid containing M. tuberculosis H37Rv genomic DNA, was passed through THP-1 human macrophages three times. Results Two of the clones recovered from this enrichment process, sur2 and sur3, exhibited significantly increased survival relative to wild-type bacteria. In coinfection experiments, the ratio of sur2 colonies to wild-type colonies was 1:1 at 0 hours but increased to 20:1 at 24 hours post phagocytosis. The ratio of sur3 colonies to wild-type colonies was 1:1 at 0 hours and 5:1 at 24 hours. The M. tuberculosis ORFs responsible for increased survival were shown to be Rv0365c for the sur2 clone and Rv2235 for the sur3 clone. These ORFs encode proteins with as-of-yet unknown functions. Conclusions We identified two M. tuberculosis ORFs which may be involved in the ability of tubercle bacilli to survive in macrophages.