Specific amplification of the 18S rRNA gene as a method to detect zebra mussel (Dreissena polymorpha) larvae in plankton samples |
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| Authors: | Frischer Marc E Hansen Andrew S Wyllie Jane A Wimbush John Murray Joanna Nierzwicki-Bauer Sandra A |
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| Institution: | (1) Skidaway Institute of Oceanography, Savannah, GA, U.S.A.;(2) Rensselaer Polytechnic Institute and Darrin Fresh Water Institute, Troy, NY, U.S.A;(3) Present address: University of Hawaii, Honolulu, HI, U.S.A;(4) Present address: California Institute of Technology, Pasadena, CA, U.S.A;(5) Present address: University of Maine, Orono, ME, U.S.A |
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| Abstract: | An important issue in the management of zebra mussel (Dreissena polymorpha) populations is early, rapid, and accurate detection of the planktonic larvae (veliger) of the zebra mussel. The goal of this study was to explore the feasibility of developing a molecular approach for the detection of zebra mussel larvae in diverse environments. In this study a Dreissena polymorpha-specific 18S ribosomal RNA gene targeted oligonucleotide primer (ZEB-715a) and Polymerase Chain Reaction (PCR) assay was developed and compared with cross-polarized microscopy as a means to detect zebra mussel veligers in plankton samples. The design of the zebra mussel-specific primer was facilitated by sequencing nearly the complete 18S rRNA gene from the zebra mussel and three other closely related freshwater Veneroids including the quagga mussel (D. bugensis), the dark false mussel (Mytilopsis leucophaeata), and the Asian freshwater clam (Corbicula fluminea). The specificity of the primer for the zebra mussel was empirically tested by using the primer as a direct probe in a blot hybridization format. A single veliger in a plankton sample could be detected by PCR using this approach. Veliger detection sensitivity using the PCR approach was estimated to be over 300 times more sensitive than cross-polarized light microscopy based techniques. Cross-polarized light microscopy and the PCR technique were used to identify the presence of zebra mussel larvae in plankton samples that were collected from a variety of natural and industrial water sources. Detection results (presence or absence) were generally consistent between the two methods. Although additional studies will be required before routine application of molecular based veliger detection technology is available, a long-term goal of this work is the application of molecular technology to the development of a field device for the routine detection and quantification of zebra mussel veligers. |
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| Keywords: | zebra mussel bivalve veliger 18S rRNA PCR |
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