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Rapid decline of PCR amplification from genomic extracts of DESS-preserved, slide-mounted nematodes

Record type: Article

Many studies use integrative methods to study both morphology and gene sequences of nematode species, yet there is little
evidence to indicate the optimum criteria for merging taxonomic and molecular protocols. Preliminary evidence suggests that standard
methods of desiccation and slide mounting nematode specimens in glycerin can sporadically result in degradation of genomic DNA.
A time series experiment was constructed in order to assess whether this degradation of genomic DNA could be recorded and quantified.
Two groups of nematode specimens were desiccated, mounted on slides, and stored at either 4?C or at room temperature for specified
time intervals. Genomic DNA was extracted and PCR was conducted to amplify a section of the 18S rRNA gene at each time point. The
resulting gel photographs were used to record the outcome of PCR and quantify the strength of amplification if successful. Results from
slide-mounted specimens were compared to PCR products derived from unmounted nematodes extracted directly from the preservative
solution at specified time intervals. The desiccation and slide mounting process appears to reduce overall band intensity after 1 day in
slide mounts. Unmounted specimens consistently exhibit high success rates of PCR and a high overall DNA content per band at all
time points, whereas slide-mounted nematodes show a decrease in the number of successful PCRs and weakening band intensity as
time progresses. Results clearly indicate a steady degradation of genomic DNA in nematodes stored in slide mounts for more than 2
weeks, whereas unmounted specimens extracted from preservative solution showed no decline in PCR success or quality. We suggest a
maximum storage period of 2 weeks on slides if mounted nematodes are to be used for molecular analyses.

Full text not available from this repository.

Citation

Bik, Holly M., Hawkins, Lawrence E., Hughes, J. Alan and Lambshead, John D. (2009) Rapid decline of PCR amplification from genomic extracts of DESS-preserved, slide-mounted nematodes Nematology, 11, (6), pp. 827-834. (doi:10.1163/156854109X422922).

More information

Published date: 2009
Keywords: DESS, DNA, glycerin, integrated methods, molecular, morphology

Identifiers

Local EPrints ID: 72651
URI: http://eprints.soton.ac.uk/id/eprint/72651
PURE UUID: 79bb757a-425d-4cbf-8978-9198ca15dde1
ORCID for Lawrence E. Hawkins: ORCID iD orcid.org/0000-0002-9236-2396

Catalogue record

Date deposited: 18 Feb 2010
Last modified: 18 Jul 2017 23:53

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