Isolation and preservation of schistosome eggs and larvae in RNAlater® facilitates genetic profiling of individuals
© Webster; licensee BioMed Central Ltd. 2009
Received: 22 September 2009
Accepted: 23 October 2009
Published: 23 October 2009
Although field-sampling procedures to capture gDNA from individual schistosome larval stages directly from their natural hosts exist, they do pose some technical and logistical challenges hampering certain epidemiological studies. The aim of this study was to develop, refine and evaluate an alternative methodology, which enables better preservation of large numbers of individual schistosome larval stages and eggs collected in low resource endemic areas, to provide PCR-quality DNA for multi-locus genetic analysis. The techniques reported here present simple and effective short-term field and long-term laboratory preservation and storage systems for individually sampled schistosome eggs and larval stages using a commercially available aqueous stabilisation reagent, RNAlater® eliminating the need for more cumbersome resources such as refrigerators, heaters and centrifuge equipment for immediate specimen processing. Adaptations to a general gDNA extraction method are described, that enables the acquisition of a gDNA extract (~50 μl), facilitating multiple molecular analyses of each sampled schistosome. The methodology provided PCR-quality mitochondrial and nuclear DNA from laboratory cercariae, miracidia and eggs that had been stored at up to 37°C for 2 weeks and at 4°C for 6 months and also from field collected samples. This present protocol provides significant epidemiological, ethical and practical advantages over existing sampling methods and has the potential to be transferred to studies on other organisms, especially where specimens are unable to be seen by the naked eye, are difficult to handle and need to be obtained from a field environment.
Advances in molecular approaches to investigate schistosome biology have added further dimensions to aspects of monitoring and surveillance of schistosomiasis. Molecular epidemiological studies have enabled pioneering investigations into many important topics possibly associated with the population genetics of these parasites , but studies can be hampered by the inaccessibility of adult schistosomes, which reside within the blood vascular system of the mammalian host. Improvements in sampling procedures have enabled the direct sampling of individual larval stages in field situations enabling researchers to avoid the problems associated with laboratory passage . However, these procedures do have some limitations such as; the need for immediate cooling and processing  and single PCR analysis .
The aim of this study was to develop and refine better methodologies for short-term tropical field and long-term laboratory preservation of large numbers of individual larval schistosomes and eggs sampled directly from natural hosts, in order to obtain gDNA suitable for multiple molecular analyses on each individual specimen. The protocol will facilitate more detailed and ethically advantageous sampling of schistosome populations for genetic profiling.
Exposure conditions of the preserved samples and resulting PCRs produced from their gDNA extracts
Tropical field (28-32°C) setting for 2 weeks + transport by plane as hold luggage
As in 9 and then storage at 4°C for up to 6 months
As in 9 and then storage at -20°C for up to 6 months
In the laboratory gDNA from each individual was extracted using the DNeasy Tissue kit (Qiagen). The samples were briefly centrifuged to re-collect them at the bottom of the Eppendorf tube and then the DNeasy animal tissue extraction protocol was followed with the following modifications. One quarter volumes of the reagents were used for the digestion and DNA precipitation steps 1-4 of the manufacturers protocol and the reagents were added directly to the tubes containing the RNAlater® preserved samples followed by incubation for just 1 h (Fig 1). In the final step the gDNA was eluted in a total of 50 μl. The concentration of the gDNA extracted was determined using a NanoDrop® ND-1000 spectrophotometer.
PCR primers and conditions
This methodology enabled the capture and preservation of individual larval stages for molecular epidemiological studies in very basic settings. PCR-quality gDNA was obtained from samples caught in small amounts of water and preserved by adding 2.5× the volume of RNAlater®, half the recommended amount by the manufacturer proving highly cost effective.
Free-swimming larvae can be difficult to catch and are often unknowingly not captured or stick to the side of the pipette tip. An advantage of this preservation technique over existing methods  is that, the presence of a single larval stage in the tube can be checked prior to preservation. This eliminates DNA contamination from multiple individuals being caught together and also PCR failures due to capture failures, saving time and resources.
The results show that the DNeasy extraction method used was not significantly affected by the presence of the water or RNAlater® allowing the digestion buffers to be added straight to the sample. Thus excluding any need for relocating, drying or re-hydrating, which is time consuming and can lead to damage and or loss of the sample. This method proved equally good for cercariae, miracidia and eggs. Storage of eggs can be valuable when there are time constraints or hatching of miracidia is proving difficult, moreover egg DNA is not always liberated when stored on Whatman FTA® cards.
PCR-quality gDNA was obtained from RNAlater® preserved samples from all time lines and temperatures tested. The results show that the preserved samples were stable at temperatures up to 37°C for up to 2 weeks. This was thought to be the maximum temperature and duration that the samples would be expected to endure following field collection before a refrigeration source was available. The samples also proved stable for up to 6 months at both 4°C and -20°C. It is predicted that the samples can remain stable for many more months, especially at -20°C as suggested in the RNAlater® protocol. This long-term preservation capability together with the fact that the individual samples can be stored in a 96-well plate format, requiring less space, provides options for long-term storage solutions. This also eliminates the immediate need to process the material, allowing greater sample sizes to be collected if required.
Positive cox1 and ITS PCRs were achieved from gDNA extracted from each individually RNAlater® preserved specimen (Table 1) even though the concentrations of gDNA were low (1.6-3.65 ng/μl for eggs/miracidia and 3.1-4.5 ng/μl for cercariae). The sequences obtained from selected amplicons corresponded to the correct organism and gene region being genotyped and the sequences were of high quality.
From each individual larval stage enough gDNA (48-50 μl) was obtained to carry out 24-25 separate PCRs enabling multiple-locus genetic analyses of the same individual and also repeat PCRs if necessary. This overcomes one major restriction of the Whatman FTA® card methodology  where only a single PCR can be routinely carried out on each individual. As both nuclear and mitochondrial DNA regions have been amplified the preservation method does not show any disadvantages/advantages in preservation of the different kinds of DNA. Although only the cox1 and ITS DNA regions were amplified no reasons exist for any limitations as to the type of population genetic analyses that could be done utilizing other DNA regions, such as microsatellites, 'barcoding', Snapshot™ and RAPD's . Another added advantage is the preservation of RNA facilitating gene expression studies, however the material would need to be treated as stated by the manufacturers recommendations to ensure RNA stabilisation.
The DNeasy extraction method proved highly efficient and effective, however it is expected that other DNA extraction methods would be suitable. The scaling down of the DNeasy reagents is cost effective for processing large populations and high throughput DNeasy 96 Plates can be used making the process more efficient, especially if specimens are originally preserved in 96-well plates.
This preservation method proved just as robust for the laboratory and field preserved material; the field trial was considered typical field-based collecting conditions. This technique will be of particular value for future biological fieldwork, especially where there is no immediate access to cold storage or equipment for immediate processing of the material. Introduction of this sampling and preservation technique may open up geographical areas that were previously excluded due to practical difficulties. Another important practical benefit is that RNAlater® is innocuous and is classified under the IATA-DGR as not dangerous goods, facilitating easier transportation by air.
To conclude, the methods and protocols described here for the collection, preservation and DNA extraction of schistosome larval stages and eggs using readily available reagents and kits are simple, robust, efficient, reliable, practical, cost effective and have proved extremely useful in a basic field laboratory. In line with Whatman FTA® cards this approach enables parasite genetic analysis without the use of laboratory animals and is in keeping with the '3Rs', the foundation of animal experimentation ethics . Furthermore this methodology allows multi-locus genotypic analysis of schistosome larval stages directly from the field environment. The development and refinement of such sampling techniques is extremely important as studies have shown that examining larval samples directly from their naturally infected hosts offers epidemiological, ethical and practical advantages [1, 2]. This is particularly topical due to the recent findings such as the surprising amount of genetic variation present within schistosome populations , the discovery and identification of new Schistosoma species  and interactions between species [5, 9]. Future studies warrant larger sample sizes of individuals and multi-locus approaches for precise identification and genetic analysis.
- cox1 :
cytochrome oxidase subunit 1
Basic Local Alignment Search Tool
International Air Transport Association: Dangerous Goods Regulations
reduce, reuse and recycle
This study was supported by the European funded Specific Targeted Research Project, CONTRAST (FP6 STREP contract no: 032203, http://www.eu-contrast.eu). The author would like to thank Dr Oumar Diaw, Dr Mohammed Seye and Dr David Rollinson for their assistance during the fieldwork. Dr David Rollinson and Dr Russell Stothard for comments and editing of the manuscript. Dr Tim Littlewood for discussions regarding field preservation methods. Mike Anderson, Jayne King and Dr Aiden Emery for maintaining the laboratory passaged material.
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