0115 966 7955 Today's Opening Times 10:30 - 17:00 (BST)

Nilaparavata Lugens (Stal) Genetic Divergence Analysis

Published: Last Edited:

Disclaimer: This essay has been submitted by a student. This is not an example of the work written by our professional essay writers. You can view samples of our professional work here.

Any opinions, findings, conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of UK Essays.

Nilaparavata lugens (Stal.)

Nilaparvata lugens is generally called as brown plant hopper or Asian rice brown plant hopper (BPH). N. lugens comes under order: Hemiptera, Suborder: Auchennorrhyncha and Family: Delphacidae. The delphacid genus Nilaparvata consists of 18 species. Nilaparvata is a crucial genus economically, with one amongst its member N. lugens being serious insect pests of rice and are cosmopolitian particularly in tropical Asia wherever rice crops are continuously cultivated (Wilson and Claridge, 1991). These insects are found throughout the year in tropical regions. In temperate areas such as in middle China, Korea and Japan, however, they do not survive within the winter season, and migrate into these countries every year with the new rice season (Park, 1973; Kisimoto, 1976; Asahina and Tsruoka, 1986; Uhm et al., 1988).

The species is mostly yellowish brown to dark brown (Fig. 1). The carina on vertex is faint and the median carina on the frons is distinct. In Nilaparvata genus the first tarsal segments bears several small spines. N. lugens is mostly seen on paddy fields. The key characters of the family are the presence of a movable spur at the base of the hind tarsi. To distinguish the major groups within the family mostly the structure of the spur is considered. In case of doubts the male genetalial characters are also used to confirm the identity of species. The male genitalia are distinctive with aedeagus slender and upturned. The parameres are distinctively shaped. In female inner margin of the valvifer VIII is rounded at the base (Wilson and Claridge, 1991).

Both nymphs and adults of BPH cause damage rice plants through intensive feeding on them. BPH conjointly transmits viruses such as rice ragged stunt (RRSV) and rice grassy stunt (RGSV) (Hibino, 1996). The foremost severe outbreak of the BPH in India occurred in Kerala state at the end of 1973 and early in 1974 (Koya, 1974; Nalinakumari and Mammen, 1975). It occurred in the ‘Kole’ lands of Trichur district and Kuttanad area in Kottayam and Alleppy districts. In many several fields the damage was so great that growers abandoned the crop (Das et al., 1972).

(d) adults on paddy plant

The partial coding sequence of mitochondrial COI gene of N. lugens was PCR amplified using the forward primer with DNA sequence 5' TAAACTTCAGGGTGACCAAAAAATCA 3' and the reverse primer with DNA sequence 5' GGTCAACAAATCATAAAGATATTGG 3'. The PCR amplification of partial COI sequence of N. lugens isolated from Kerala, India yielded a product with 658 bp. The DNA sequence obtained, its conceptual translation product, nucleotide BLAST, peptide BLAST and Chromatogram are presented in figures (2-6). The sequence was deposited within the GenBank with a GenBank Accession No. KJ796483.

> Nilaparvata lugens cytochrome oxidase subunit I gene | Voucher SRCUNILA01| partial cds; mitochondrial| 658 bp| Accession No. KJ796483

> Nilaparvata lugens |Voucher SRCUNILA01| cytochrome oxidase subunit I, partial (mitochondrion) peptide| 219 AA.

Nilaparvata lugens voucher AIN18001AP1 Cytochrome oxidase subunit I (COX1) gene, partial cds; mitochondrial Sequence ID: gb| KC858992.1| Nilaparvata lugens| Length: 658

Nilaparvata lugens cytochrome oxidase subunit I (mitochondrion) GenPeptGraphics Sequence ID: lcl|82965| Nilaparvata lugens|Length: 219

The COI nucleotide sequence analysis revealed the composition of nucleotides in the COI gene of N. lugens isolated from Kerala (Table 2). The COI sequence of N. lugens showed bias to nucleotide AT, with following composition of nucleotides T=27.9%, C=15.9%, A=35.3% and G=20.9%. The COI nucleotide composition analysis showed the variation in composition of each nucleotide of N. lugens isolated from Kerala and geographically isolated populations like Karnataka (KC858992), China (AB572318, KC476395 and KC476394).

Alyses of Evolutionary Divergence were conducted using the Maximum Composite Likelihood model. The analysis concerned 16 nucleotide sequences. Codon positions included were 1st+2nd+3rd+Noncoding. All positions containing gaps and missing data were eliminated. There have been a total of 258 positions in the final data set. Evolutionary analyses were conducted in MEGA6. The evolutionary divergence analysis of N. lugens depicts the degree of divergence in the Delphacidae family of different geographically isolated populations of N.lugens is shown in table (3).

From the data given in the table (3) it is clear that the N. lugens showed 0.02% evolutionary divergence with N. lugens isolated from Karnataka and the species from China. Mongoliana serrata species is the one which showed a maximum of 2.41% of evolutionary divergence with N. lugens isolated from Kerala.

The phylogeny tree generated using NJ method showing the phylogenetic position of N. lugens isolated from Kerala is given in figure (7). Phylogenetically N. lugens (JN391181) and (AB572314) showed to be the closest relatives of N. lugens of Kerala. They were arranged in were aligned in single clad and divided into two sub branches separately.

Discussion

The sample were successfully sequenced using the forward and reverse primers to get forward and reverse sequences of 658 bp. The sequence identification with the NCBI BLAST tool disclosed that closest similarity of 99% is shown by N. lugens (GenBank accession No. KC858992) isolates from Karnataka. The above data with NCBI BLAST tool revealed that no 100% sequence similarity for COI gene are available in the data base. It can be interpreted that the resultant sequence obtained for the N. lugens Kerala is novel. The COI sequence obtained during this study showed variation with other species of identical family pointing its use as a DNA barcode to spot the species. The COI sequence could also be used for evolutionary studies and host insect relation studies of N. lugens. The most of the hemipteran species mitogenomes nucleotide compositions are significantly biased toward A and T. The mitochondrial genome of hemipteran species has considerable variation in base composition among different hemipteran species (Zhang et al., 2013). The COI nucleotide sequence analysis of N. lugens isolated from Kerala and other geographically isolated population also showed 63 to 65% AT content in the COI sequence which is varied from the total AT content of J strand which is 70 to 74.42%. These results indicated that, in the hemiptera the AT content of COI gene will be less compared to the total AT content of J strand. In the nucleotide triplet code, there is strong compulsion in the nucleotide changes in second position of all codons and first position of many codons. Due to the degenerative character of the triplet code third position of many codons and first position of some codons is less constraint.

The variations in the strong constraint positions lead to the variations in the amino acids sequence. But the variations in the less constraint position will not affect (silent) the phenotype and these less constrained codon positions evolved at high rate (Nei, 1987; Irwin et al., 1991).

The genetic divergence analysis revealed the genetic difference within the species N. lugens and between the related species of order Hemiptera. The COI sequence of N. lugens showed considerable variations with the related species. Thus the COI sequence isolated during this study can be used as a barcode to spot this insect species. Within the evolution tree the N. lugens isolated from totally different geographical locations are formed from a common ancestor. This indicates that the N. lugens is a monophyletic species.


To export a reference to this article please select a referencing stye below:

Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.
Reference Copied to Clipboard.

Request Removal

If you are the original writer of this essay and no longer wish to have the essay published on the UK Essays website then please click on the link below to request removal:


More from UK Essays

We can help with your essay
Find out more
Build Time: 0.0019 Seconds