Morphological and molecular characterization of tropical Meloidogyne species in Brazil
Carvalho, Vanessa Rafaela de et al. (2020), Morphological and molecular characterization of tropical Meloidogyne species in Brazil, Dryad, Dataset, https://doi.org/10.5061/dryad.v6wwpzgtg
The morphological identification of nematodes species, followed the criteria established in their original descriptions (Eisenback and Hirschmann, 1981). Ten fully developed and milky females per species were removed from the roots and stored in water for perineal cuts. Each female was transferred to a slide containing a drop of lactic acid (45%) under a stereomicroscope and a cross section was made in the anterior region of each one, with the aid of a scalpel, for the complete extravasation of their internal content. The perineal region was dissected and transferred to a slide, containing glycerin (100%), sealed and labeled (Hussey & Barker 1973). Specimens with predominant characteristics of the group were selected and used. The shape and appearance of the perineal region, dorsal arch, dorsal streaks and lines of the lateral fields of the females were the morphological characteristics observed. The nematode males were obtained from processed roots, whose suspension was observed under a stereomicroscope.Ten males were recovered from the suspension, by species, using a fishing rod and transferred to a temporary, sealed and labeled blade containing water (Hussey & Barker 1973). The identification of the nematode males was based on their anterior region. Morphological characteristics of females and males were analyzed using an Olympus “BX50” microscope with an attached Olympus “DP72” camera.
Genomic DNA extraction and common PCR from infective juveniles
The genomic DNA of 50 infective juveniles of four Meloidogyne species (Table 1) was extracted in 50 µl of 0.85% NaCl, by Worm Lysis Buffer (WLB) (Carvalho et al., 2019). These samples were placed in solution with KCl (50 mM), Tris (10 mM pH 8.2), MgCl2 (2.5 mM), Tween 20 (0.45%) and proteinase K (200 mg/ml) at -70ºC for 15 minutes, incubated for one hour at 60ºC, 15 minutes at 95ºC and stored at -20ºC. The quality of the extracted DNA was verified by a universal primer D2a and D3b (Nadler et al., 1999) amplifying the D2 and D3 of the expansion region of the 28D rDNA nuclear gene. Positive samples, for the primers D2a and D3b, and the DNA of M. enterolobii, M. exigua, M. incognita, M. javanica and M. paranaensis were amplified with specific primers (Table 2). The amplification reactions were carried out with 12.5 μl of Dropsq (Neobio), 1 μl of each primer [10 p/mol] and 7.5 μl of nuclease-free water 3 μl of the DNA mixture totaling a 25 μl reaction.
Multiplex PCR and primer validation and molecular identification
Meloidogyne exigua, M. incognita, M. javanica and M. paranaensis were detected and identified, simultaneously, by PCR, each, quickly, with the four pairs of specific primers. The primers Fjav-1 and Rjav-1, Fexi-1 and Rexi-1, Finc-1 and Rinc-1 and Fpar-1 and Rpar-1 were used for the multiplex PCR for M. exigua, M. incognita, M. javanica, and M. paranaensis, respectively. The 500 bp fragment, resulting from universal primers, is an internal positive of DNAr 28S D2/D3.The amplification reactions were performed in 0.2 ml of PCR tubes with reaction volumes of 25 μl. The main mixture had 12.5 μl of drq (Neobio), 0.5 μl of each primer [10 w/mol], 5.5 μl of nuclease-free water and 3 μl of the DNA mixture. The DNA quality was verified with the fragment D2/D3 extension of the 28S rDNA to avoid false negatives in the specific PCRs by species of nematode. The confidence of the nematode identification using the primers (Table 2), based on PCR withthe the extraction of genomic DNA from 50 infective juveniles to verify amplification (Fig. 3) and specific ones was greater.
Five μl of PCR product from each sample was loaded onto the agarose gel. The DNA bands were stained with GelRed (Neobio) and visualized and photographed on a UV transilluminator (Major Science). The remaining products, per sample, were stored at -20°C.
In PCR reactions it is necessary to work with good quality DNA. And to know the efficiency of each process in the analysis of DNA, such as the extraction, quantification and purification of DNA. It is necessary to extract the intact DNA in order not to break the bonds, since these are responsible for the genetic information. Quantification involves estimating the DNA concentration obtained, which depends on the type and quantity of sample available.
DNA quantification by spectrophotometry is able to determine the average concentrations of nucleic acids DNA or RNA present in a sample, as well as their purity. To accurately assess the quality of the sample, 260/280 or 260/230 indices should be analyzed in combination with overall spectral quality. Pure nucleic acids typically produce a ratio of 260/280 to approximately 1.8 and a ratio of 260/280 to approximately 2.0 for DNA. The 260/230 degree of purity is a second measure of DNA purity with the values of a pure nucleic acid generally in the range of 1.8-2.2.
The columns H onwards do not contain information, although column headings are included.