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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Jul 26;4(2):2765–2766. doi: 10.1080/23802359.2018.1551076

A complete mitochondrial DNA genome of whitefly species (Hemiptera: Aleyrodidae) from Litchi chinensis

Hua-Ling Wang a,b, Teng Lei a, Yin-Quan Liu a,
PMCID: PMC6816494  PMID: 31709305

Abstract

A novel complete mitochondrial genome (mitogenome) of whitefly species, collected from Litchi chinensis at Fujian province of China (hereafter whitefly_Litchi chinensis _China) (GenBank accession number: MH999477), was described in this study. The mitogenome of whitefly_Litchi chinensis _China is 15,360 bp in length and contains 13 protein-coding genes, 21 transfer RNAs, 2 ribosomal RNAs and a non-coding AT-rich region (D-loop). The arrangement of mitochondrial genes of whitefly_Litchi chinensis_China are identical with Aleurochiton aceris, but remarkably different from the mitogenomes of the other whitefly genus. Most protein-coding genes (PCGs) start with ATN, except for nad2, cox2 and atp6 genes starting with TTG, GTG, and TTG, respectively; 10 of the 13 PCGs use the typical stop codon TAN, whereas cox1, and cox2 stop with a single T. Phylogenetic analyses based on 13 PCGs support the close relationship of the sample with Aleurochiton aceris, which would provide us further insights on the taxonomy and phylogeny of Aleyrodidae.

Keywords: Mitochondrial genome, phylogeny, whitefly, Litchi chinensis


Whiteflies (Order Hemiptera, Family Aleyrodidae) can be considered as the second most important vectors due to their capacity to transmit many plant viruses (España and López-Moya 2014) and comprise more than 1,156 species in 126 genera (Mound and Halsey 1978). However, the whitefly species of many countries of the world are poorly known. For the whitefly systematics, it is in veritable disarray because variable pupal morphology can be altered by environmental factors which have been found to be common in many genera, especially in the subfamily Aleyrodinae (Neal and Bentz 1999). Consequently, most whitefly species in the Aleyrodinae have been arbitrarily placed in various genera over the years with no clear idea of their phylogenetic relationships (Russell 1957; Mound 1963; Mound and Halsey 1978; Gill 2012). Such instance drive taxonomists to seek the proper molecular markers for aiding inferring the systematics and evolutionary history of whitefly.

To enrich the whitefly molecular markers, in this study, a newly complete mitogenome of whitefly belonging to the subfamily Aleyrodinae collected from Lichi at Fujian province, China (hereafter Whitefly_Litchi chinensis _China) was determined. The sample was deposited at the Key Laboratory of Agricultural Entomology, Institute of Insect Science, Zhejiang University, Hangzhou, China. The total genomic DNA was extracted from a single individual using the Qiagen DNeasy Blood and Tissue Kit Extraction Kit (Germany) (Wang et al. 2013). The DNA was then subjected to conduct next-generation sequencing which generated 20GB raw pair-end reads (Illumina HisSeq 2500; 2*150bp, Shanghai, China). The clean reads were assembled by NOVOPlasty software (Dierckxsens et al. 2017) with setting up available whitefly mitogenomes as references. The resultant contigs were annotated using softwares of Geneious (Drummond et al. 2011), tRNAscan-SE (Lowe and Eddy 1997) and website of MITOS (Bernt et al. 2013).

The whole mitochondrial genome is a circular molecule of 15,360 bp (30.98% A, 43.61% T, 14.84% G, and 11.02% C) in size, and contains 13 PCGs, 21 tRNA genes (t-RNA-Glu is absent), and two rRNA genes and a non-coding AT-rich region (D-loop) (GenBank accession number: MH999477). A 1,536 bp of the cox1 gene shows 77% sequence similarity to a cox1 sequence of Aleurochiton aceris in GenBank (accession number AY572538.1). Remarkedly, the gene arrangement and orientation are identical with the Aleurochiton aceris but differ from the other whitefly species. Most of PCGs start with ATN, except for nad2, cox2 and atp6 genes starting with TTG, GTG, and TTG, respectively; 10 of the 13 PCGs use the typical stop codon TAN, whereas two PCGs (cox1 and cox2) stop with the incomplete codon T.

In addition, with the maximum-likelihood (ML) and Bayesian inference (BI) methods through RAxML (version 8.2.4) (Stamatakis 2006) and MrBayes (version 3.2.6) (Ronquist and Huelsenbeck 2003), phylogenetic trees were constructed using 13 PCGs of mitogenomes from the closely related whitefly species. In the commands of MrBayes and RAxML, the data were partitioned by codons based on the partition schemes derived from PartitionFinder 2 (Lanfear et al. 2016). The resultant ML and BI trees share the same topologies and show that our specimen (whitefly_ Litchi chinensis _China _MH999477) cluster together with Aleurochiton aceris (Figure 1).

Figure 1.

Figure 1.

Maximum likelihood (ML) and Bayesian inference (BI) phylogenetic trees inferred from the nucleotide sequence data of mitogenomic 13 PCGs. *100/1.00(BP/BPP)

Disclosure statement

The authors report no conflict of interest. The authors alone are responsible for the content and writing of this paper.

References

  1. Bernt M, Donath A, Jühling F, Externbrink F, Florentz C, Fritzsch G, Pütz J, Middendorf M, Stadler PF. 2013. MITOS: improved de novo metazoan mitochondrial genome annotation. Mol Phylogenet Evol. 69:313–319. [DOI] [PubMed] [Google Scholar]
  2. Dierckxsens N, Mardulyn P, Smits G. 2017. NOVOPlasty: de novo assembly of organelle genomes from whole genome data. Nucleic Acids Res. 45:e18–e18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Drummond AJ, Ashton B, Buxton S, Cheung M, Cooper A, Duran C, Field M, Heled J, Kearse M, Markowitz S. 2011. Geneious, version 5.4. Auckland, New Zealand: Geneious. [Google Scholar]
  4. España MU, López-Moya JJ. 2014. Interference with insect transmission to control plant-pathogenic viruses, Plant Virus-Host Interaction. Elsevier. [Google Scholar]
  5. Gill R. 2012. A preliminary report on the World species of Bemisia Quaintance and Baker and its congeners (Hemiptera: Aleyrodidae) with a comparative analysis of morphological variation and its role in the recognition of species. Insecta Mundi. 219:1–99. [Google Scholar]
  6. Lanfear R, Frandsen PB, Wright AM, Senfeld T, Calcott B. 2016. PartitionFinder 2: new methods for selecting partitioned models of evolution for molecular and morphological phylogenetic analyses. Molr Biol Evol. 34:772–773. [DOI] [PubMed] [Google Scholar]
  7. Lowe TM, Eddy SR. 1997. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25:955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mound LA. 1963. Host-correlated variation in Bemisia tabaci (gennadius)(homoptera: aleyrodidae). Physiol Entomol. 38:171–180. [Google Scholar]
  9. Mound LA, Halsey SH. 1978. Whitefly of the world. A systematic catalogue of the Aleyrodidae (Homoptera) with host plant and natural enemy data. John Wiley and Sons. [Google Scholar]
  10. Neal JW Jr, Bentz JA. 1999. Evidence for the stage inducing phenotypic plasticity in pupae of the polyphagous whiteflies Trialeurodes vaporariorum and Bemisia argentifolii (Homoptera: Aleyrodidae) and the raison d'etre. Ann Entomol Soc Am. 92:774–787. [Google Scholar]
  11. Ronquist F, Huelsenbeck JP. 2003. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 19:1572–1574. [DOI] [PubMed] [Google Scholar]
  12. Russell LM. 1957. Synonyms of Bemisia tabaci (Gennadius)(Homoptera: Aleyrodidae). Bull of Brooklyn Entomol Soc. 52:122–123. [Google Scholar]
  13. Stamatakis A. 2006. RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 22:2688–2690. [DOI] [PubMed] [Google Scholar]
  14. Wang HL, Yang J, Boykin LM, Zhao QY, Li Q, Wang XW, Liu SS. 2013. The characteristics and expression profiles of the mitochondrial genome for the Mediterranean species of the Bemisia tabaci complex. BMC Genomics. 14:401. [DOI] [PMC free article] [PubMed] [Google Scholar]

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