Molecular approaches for monitoring potentially toxic marine and freshwater phytoplankton species
被引:42
作者:
Humbert, J. F.
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机构:
INRA, UMR BIOEMCO, F-75005 Paris, FranceINRA, UMR BIOEMCO, F-75005 Paris, France
Humbert, J. F.
[1
]
Quiblier, C.
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机构:
MNHN, FRE Cyanobacteries Cyanotoxines & Environm 3206, CP39, F-75231 Paris 05, France
Univ Paris Diderot, F-75013 Paris, FranceINRA, UMR BIOEMCO, F-75005 Paris, France
Quiblier, C.
[2
,3
]
Gugger, M.
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机构:
Inst Pasteur, Dept Microbiol, F-75015 Paris, France
CNRS, URA2172, F-75015 Paris, FranceINRA, UMR BIOEMCO, F-75005 Paris, France
Gugger, M.
[4
,5
]
机构:
[1] INRA, UMR BIOEMCO, F-75005 Paris, France
[2] MNHN, FRE Cyanobacteries Cyanotoxines & Environm 3206, CP39, F-75231 Paris 05, France
[3] Univ Paris Diderot, F-75013 Paris, France
[4] Inst Pasteur, Dept Microbiol, F-75015 Paris, France
Harmful phytoplankton species are a growing problem in freshwater and marine ecosystems, because of their ability to synthesize toxins that threaten both animal and human health. The monitoring of these microorganisms has so far been based on conventional methods, mainly involving the microscopic counting and identification of cells, and using analytical and bioanalytical methods to identify and quantify the toxins. However, the increasing number of microbial sequences in the GeneBank database and the development of new tools in the last 15 years nowadays enables the use of molecular methods for detection and quantification of harmful phytoplankton species and their toxins. These methods provide species-level identification of the microorganisms of interest, and their early detection in the environment by PCR techniques. Moreover, real time PCR can be used to quantify the cells of interest, and in some cases to evaluate the proportion of toxin-producing and non-toxin-producing genotypes in a population. Recently, microarray technologies have also been used to achieve simultaneous detection and semi-quantification of harmful species in environmental samples. These methods look very promising, but so far their use remains limited to research. The need for validation for routine use and the cost of these methods still hamper their use in monitoring programs.
机构:
CNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France
Araoz, Romulo
Molgo, Jordi
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CNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France
Molgo, Jordi
de Marsac, Nicole Tandeau
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机构:
Inst Pasteur, Unite Cyanobacteries, CNRS, URA 2172, F-75724 Paris 15, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France
机构:
CNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France
Araoz, Romulo
Molgo, Jordi
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机构:
CNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France
Molgo, Jordi
de Marsac, Nicole Tandeau
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h-index: 0
机构:
Inst Pasteur, Unite Cyanobacteries, CNRS, URA 2172, F-75724 Paris 15, FranceCNRS, Inst Neurobiol Alfred Fessard, FRC2118, Neurobiol Cellulaire & Mol Lab,UPR9040, F-91198 Gif Sur Yvette, France