8 research outputs found

    SSU Ribosomal DNA-Based Monitoring of Nematode Assemblages Reveals Distinct Seasonal Fluctuations within Evolutionary Heterogeneous Feeding Guilds

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    <div><p>Soils are among the most complex, diverse and competitive habitats on Earth and soil biota are responsible for ecosystem services such as nutrient cycling, carbon sequestration and remediation of freshwater. The extreme biodiversity prohibits the making of a full inventory of soil life. Hence, an appropriate indicator group should be selected to determine the biological condition of soil systems. Due to their ubiquity and the diverse responses to abiotic and biotic changes, nematodes are suitable indicators for environmental monitoring. However, the time-consuming microscopic analysis of nematode communities has limited the scale at which this indicator group is used. In an attempt to circumvent this problem, a quantitative PCR-based tool for the detection of a consistent part of the soil nematofauna was developed based on a phylum-wide molecular framework consisting of 2,400 full-length SSU rDNA sequences. Taxon-specific primers were designed and tested for specificity. Furthermore, relationships were determined between the quantitative PCR output and numbers of target nematodes. As a first field test for this DNA sequence signature-based approach, seasonal fluctuations of nematode assemblages under open canopy (one field) and closed canopy (one forest) were monitored. Fifteen taxa from four feeding guilds (covering ∼ 65% of the free-living nematode biodiversity at higher taxonomical level) were detected at two trophic levels. These four feeding guilds are composed of taxa that developed independently by parallel evolution and we detected ecologically interpretable patterns for free-living nematodes belonging to the lower trophic level of soil food webs. Our results show temporal fluctuations, which can be even opposite within taxa belonging to the same guild. This research on nematode assemblages revealed ecological information about the soil food web that had been partly overlooked.</p> </div

    Development and testing of a nematode family-specific primer combination.

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    <p>Here we use the Metateratocephalidae (one bacterivorous family harboring the <i>Metateratocephalus</i> and <i>Euteratocephalus</i> genera) as an example of primer development. (<b>A</b>) All primers were designed to have optimal annealing temperature (T<sub>a</sub>) of 63°C, with C<sub>t</sub> values varying at temperatures above and below the target T<sub>a</sub>. (<b>B</b>) Specificity test of a Metateratocephalidae primer combination with plasmid DNAs from three target species, SSU rDNA fragments from 11 potential false positives (as selected by ARB <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-Ludwig1" target="_blank">[39]</a>) and a negative water control. Clade numbers are according to Van Megen <i>et al</i>. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-VanMegen1" target="_blank">[23]</a>. In the quantitative PCR graph the gap between the target and the non-target signal (ΔC<sub>t</sub>) is shown. (<b>C</b>) Pictures of the head region of a representative of both genera. (<b>D</b>) The relationship between C<sub>t</sub> values and numbers of nematodes for quantification of densities. A linear relationship between C<sub>t</sub> values and numbers of nematodes till <sup>1</sup>/<sub>1,000</sub> part of a single nematode is shown (equivalent to a single nematode cell harboring ∼50 copies of the ribosomal DNA cistron). Hand-picked individuals of <i>Metateratocephalus</i> (purple circles) and <i>Euteratocephalus</i> (blue squares) were used to quantify the Metateratocephalidae-specific primers.</p

    Temporal patterns of fungivorous nematode families.

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    <p>Seasonal variation in densities for fungivores in the field (<b>A</b>) and in the forest (<b>B</b>). Please note that the <i>y</i>-axis scales differ. Aphelenchidae (Aphe, blue), Aphelenchoididae (Acho, red), and two genera belonging to Diphtherophoridae –<i>viz</i>. <i>Tylolaimophorus</i> (Tylo, green) and <i>Diphtherophora</i> (Diph, yellow)– show different patterns over the seasons between open and close canopies. As these taxa represent all observed fungivores, a partial Mantel analysis performed in a matrix describing the community structure in the field (open canopies, matrix Y) and in the forest (close canopies, matrix X) using the squared Euclidean distance was performed using the total entries and the same set of entities. A positive association between the matrices is indicated over the seasons by observed Z greater than average Z from randomized runs (<i>P</i> = 0.0297).</p

    Quantitative coverage of the DNA-based tool using environmental samples.

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    <p>Logarithm of the total of individuals as detected by optical microscopy (<i>x</i>-axis) plotted against the logarithm of the total of individuals as estimated by quantitative PCR (<i>y</i>-axis). The correlations of quantitative PCR with classical analyses seem to be accurate, with no Studentized residuals higher than | 2 |. The solid line shows the trend of all data and the two dashed lines show the boundaries of one-order-of-magnitude precision. The dotted line represents an equal amount of nematodes for both methods. Such a coverage is expected to be lower than 100% as obligate plant parasites were not included, although the fungivorous Aphelenchidae and Aphelenchoididae may harbor facultative plant parasites as shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone-0047555-t002" target="_blank">Table 2</a>. Given that taxa like Rhabditidae, Qudsianematidae or Nordiidae appear to be both poly- and paraphyletic <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-VanMegen1" target="_blank">[23]</a>, <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-Holterman2" target="_blank">[65]</a>, no rDNA-based detection assay on family level could be developed for those nematodes.</p

    Overview of nematode diversity at genus level (microscopic analysis) in the topsoil (depth 0–25 cm) of the former arable field and the adjacent pristine beech forest.

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    <p>Obligate plant-parasitic nematodes are shown in grey [taxa ara given in brackets] and are not included in the molecular part of this research. Only the genera marked by ‘q’ are included in the quantitative PCR analysis and for most of these genera quantitative ranges (‘r’) are available (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone-0047555-g004" target="_blank">Fig. 4</a> and text for more details). For the taxonomy of the families we adhered to De Ley <i>et al</i>. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-DeLey1" target="_blank">[66]</a>.</p

    Temporal patterns of bacterivorous, omnivorous and predatory nematode families.

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    <p>We determined DNA-based variation in the nematode densities per 100 ml soil (note differences in <i>y</i>-axes) of representatives from seven bacterivorous families: Teratocephalidae, Prismatolaimidae, Cephalobidae, Plectidae (<i>i.e.</i>, all Plectidae excl. <i>Anaplectus</i> and ‘<i>Anaplectus</i>’, both in a dashed gray box), Alaimidae, Metateratocephalidae, Monhysteridae; the omnivorous family Dorylaimidae (D3 region <i>sensu </i><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-Holterman2" target="_blank">[65]</a>); and the predatory families Mononchidae (M3, <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-Holterman2" target="_blank">[65]</a>) and Mylonchulidae. Sampling weeks as <i>x</i>-axes (constant scales); samples from the field are represented by orange triangles and samples from the forest by green diamonds. Trends are given as two-period moving averages: the averaged 2<sup>nd</sup> and 3<sup>rd</sup> data points are portrayed by the 1<sup>st</sup> data point and so forth.</p

    Molecular overview of the nematode families and genera monitored in our study.

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    <p>Specificity of primer combinations is expressed as the gap between the C<sub>t</sub> value of the latest target and the C<sub>t</sub> value of the earliest non-target (ΔC<sub>t</sub> expressed in number of PCR cycles). For relationship between C<sub>t</sub> value and number of target nematodes see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone-0047555-g004" target="_blank">Fig. 4</a>, and Materials and Methods in ‘<i>Relationships between C<sub>t</sub> values and numbers of target nematodes</i>’.</p><p>B: bacterivore, F: fungivore, FP: facultative plant parasite (only for nematodes where this guild occurred in combination with fungivory), O: omnivore, P: predator; N/A: no quantitative PCR signal produced by non-target(s); <sup>*</sup>: number of genera within one family assessed by qPCR (families as in De Ley <i>et al</i>. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047555#pone.0047555-DeLey1" target="_blank">[66]</a>); **: as <i>Mylonchulus</i> is expected to occur in this area, its family has been included as additional taxon.</p

    Precipitation and temperature in relation to total nematode densities in open (field) and closed (forest) canopies.

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    <p>Weekly averages of daily temperature (red) and total rainfall over 21 days before sampling (blue) as measured by the Royal Dutch Meteorological Institute (KNMI) are shown above. At the bottom, average nematode densities per 100 ml of soil from a since 25 years abandoned arable field (open canopy, yellow bars) and adjacent pristine beech forest (close canopy, green bars) are given. Sites sampled in 2009 at regular intervals between March 17 (week 1) and December 18 (week 39).</p
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