DEVELOPMENT OF A SPECIFIC QUANTITATIVE REAL-TIME PCR ASSAY TO MONITOR CHLORELLA DNA: A CASE STUDY FROM MAMMOTH CAVE NATIONAL PARK, KENTUCKY, USA

被引:0
作者
Fowler, Richard F. [1 ,2 ]
机构
[1] Western Kentucky Univ, WATERS Lab, Appl Res & Technol Program, Bowling Green, KY 42101 USA
[2] Western Kentucky Univ, Hoffman Environm Res Inst, Appl Res & Technol Program, Bowling Green, KY 42101 USA
关键词
Chlorella; DNA; qPCR; phytoplankton; resource management; water quality; SYBR-GREEN-I; ALGAE; QUANTIFICATION; GROWTH;
D O I
暂无
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Richard F. Fowler: Development of a Specific Quantitative Real-Time PCR Assay to Monitor Chlorella DNA: A Case Study front Mammoth Cave National Park, Kentucky, USA Estimates of phytoplankton abundance are important parameters watched by stewards of water quality and freshwater ecology in rivers, streams, and reservoirs. A targeted phytoplankton assay for Chlorella DNA was developed to estimate the abundance of the predominant species of green algae in surface waters of Mammoth Cave National Park (MAGA) in Kentucky, USA. The phytoplankton community in the Green River in MACA has been shown to consist of 95% Chlorella sp. (Wullschlegger et al., 2003). Chlorella 188 rRNA gene sequences were amplified and quantified using Quantitative Real-Time PC R (qPCR) with primers specific for the family Chlorellaceae in the class Trebouxiophyceae, order Chlorellales. Concentrations of Chlorella DNA in river water samples were measured by comparison to a standard curve generated by DNA extracted from a live laboratory culture of C. vulgaris. DNA isolated from other sources including bacteria, amoebae, fungi, decapods, insects, cave sediment, and a different green alga, Chlamydomonas, produced no PCR products and thus did not interfere with the detection and quantification of Odor-elk, DNA. The assay proved quantitative over more than four orders of magnitude with a method detection limit (MDL) of approximately 2.3 x 10(4) cells/L. Presence or absence of Chlorella DNA could be demonstrated at concentrations ten to 100 times lower than the calculated MDL. Chlorella was detected in lampenflora samples from three tourist trails, and Chlorella was absent from sediment samples off tourist trails that were known to contain high concentrations of bacterial DNA. Demonstration of the utility of the technique was illustrated by a case study in Mammoth Cave National Park to determine Chlorella concentrations at various sampling sites of karst surface streams where invasive zebra mussels are a threat to native species.
引用
收藏
页码:381 / 390
页数:10
相关论文
共 14 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
CREITZ GI, 1955, J MAR RES, V14, P211
[3]  
FOWLER R, 2008, FINAL REPORT NATL CA
[4]   Genetic evidence of "American" and "European"' type symbiotic algae of Paramecium bursaria Ehrenberg [J].
Hoshina, R ;
Kato, Y ;
Kamako, S ;
Imamura, N .
PLANT BIOLOGY, 2005, 7 (05) :526-532
[5]   Eu-Chlorella large subunit rDNA sequences and group I introns in ribosomal DNA of the paramecian symbiotic alga NC64A [J].
Hoshina, Ryo ;
Imamura, Nobutaka .
PHYCOLOGICAL RESEARCH, 2008, 56 (01) :21-32
[6]   Comparison of real-time PCR with SYBR Green I or 5′-nuclease assays and dot-blot hybridization with rDNA-targeted oligonucleotide probes in quantification of selected faecal bacteria [J].
Malinen, E ;
Kassinen, A ;
Rinttilä, T ;
Palva, A .
MICROBIOLOGY-SGM, 2003, 149 :269-277
[7]  
MARSHALL HG, 2005, STANDARD METHODS EXA, V10, P26
[8]  
Mulec J, 2009, J CAVE KARST STUD, V71, P109
[9]  
OSBORN KE, 2005, STANDARD METHODS EXA, V1, P17
[10]   Real-time PCR based on SYBR-Green I fluorescence: An alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions [J].
Ponchel, F ;
Toomes, C ;
Bransfield, K ;
Leong, FT ;
Douglas, SH ;
Field, SL ;
Bell, SM ;
Combaret, V ;
Puisieux, A ;
Mighell, AJ ;
Robinson, PA ;
Inglehearn, CF ;
Isaacs, JD ;
Markham, AF .
BMC BIOTECHNOLOGY, 2003, 3 (1)