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. 2019 Dec 9;20(1):954.
doi: 10.1186/s12864-019-6281-1.

Genomic insights into mite phylogeny, fitness, development, and reproduction

Affiliations

Genomic insights into mite phylogeny, fitness, development, and reproduction

Yan-Xuan Zhang et al. BMC Genomics. .

Abstract

Background: Predatory mites (Acari: Phytoseiidae) are the most important beneficial arthropods used in augmentative biological pest control of protected crops around the world. However, the genomes of mites are far less well understood than those of insects and the evolutionary relationships among mite and other chelicerate orders are contested, with the enigmatic origin of mites at one of the centres in discussion of the evolution of Arachnida.

Results: We here report the 173 Mb nuclear genome (from 51.75 Gb pairs of Illumina reads) of the predatory mite, Neoseiulus cucumeris, a biocontrol agent against pests such as mites and thrips worldwide. We identified nearly 20.6 Mb (~ 11.93% of this genome) of repetitive sequences and annotated 18,735 protein-coding genes (a typical gene 2888 bp in size); the total length of protein-coding genes was about 50.55 Mb (29.2% of this assembly). About 37% (6981) of the genes are unique to N. cucumeris based on comparison with other arachnid genomes. Our phylogenomic analysis supported the monophyly of Acari, therefore rejecting the biphyletic origin of mites advocated by other studies based on limited gene fragments or few taxa in recent years. Our transcriptomic analyses of different life stages of N. cucumeris provide new insights into genes involved in its development. Putative genes involved in vitellogenesis, regulation of oviposition, sex determination, development of legs, signal perception, detoxification and stress-resistance, and innate immune systems are identified.

Conclusions: Our genomics and developmental transcriptomics analyses of N. cucumeris provide invaluable resources for further research on the development, reproduction, and fitness of this economically important mite in particular and Arachnida in general.

Keywords: Acari; Development; Ecology; Evolution; Feeding; Genome; Sex.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Comparative genomics, phylogenesis, and evolution of the Acari species. a. The phylogenomic tree of mites based on predicted protein data with divergence time estimates) and. Genomic data from six species of Acari were included: two tick species (Ixodes scapularis and Rhipicephalus microplus, order Ixodida), two predatory mite species (Metaseiulus occidentalis and Neoseiulus cucmeris, order Mesostigmata), and two acariform mites (Tetranychus urticae, order Trombidiformes and Sarcoptes scabiei, order Sarcoptiformes). Two non-mite arachinids were also included: Stegodyphus mimosarum (Scorpiones Mesobuthus martensii (Araneae); full genomic data for other orders of Arachnida not available. Limulus polyphemus (Xiphosura) was used as an outgroup taxon, with the possible Limulus polyphemus-arachnida split 490 (468–520) MYA as one fossil calibration. b. Comparison of the gene families of five sequenced species within the Subclass Acari. A total of 2141 gene families were shared by all the species N. cucumeris (23.24% of 9214), M. occidentalis (25.07% of 8539), I. scapularis (28.94% of 7398), R. microplus (42.42% of 5047) and T. urticae (35.27% of 6070). c. The genome microsynteny between two predatory mites: N. cucumeris and M. occidentalis. 142 N. cucumeris scaffolds (> 10 kb) had strong co-linearity with 224 M. occidentalis scaffolds, spanning 137.85 Mb and 123.58 Mb of the N. cucumeris and M. occidentalis genomes, respectively
Fig. 2
Fig. 2
Life cycle, reproduction, and genetic system of the predatory mite Neoseiulus cucumeris. Both males and females go through one 6-legged larval stage and two 8-legged nymphal stages (first or protonymph and second or deutonymph) without obvious differences in morphology. Adult males are smaller than females and have more a pointed posterior end. Mating is required for oviposition for female mites, which produce fertilized eggs (2n). In the early embryo, the paternal genome is eliminated in eggs destined to be males in this parahaploid species
Fig. 3
Fig. 3
The organization of Hox genes of Neoseiulus cucumeris and other chelicerate species. The forward arrows represent the genes on the forward strand while the reverse arrows represent the genes on the reverse strand. The lines indicate the genes on the same scaffold. The length of the lines does not represent the physical length
Fig. 4
Fig. 4
The detoxification and stress-resistance related gene superfamilies identified in N. cucumeris, showing phylogenetic relationships (in protein sequences). a of cytochrome P450 (CYP450), b of glutathione-S-transferase (GST) and C of carboxyl/ cholinesterase (CCE). This is maximum likelihood tree. Numbers at nodes are bootstrap values. The genes with red background are from N. cucumeris. The genes with blue background are from M. occidentalis. The genes with cyan background are from I. scapularis. The genes with purple background are from D. melanogaster

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References

    1. Zhang ZQ. Animal biodiversity: an update of classification and diversity in 2013. Zootaxa. 2013;3703:5–11. doi: 10.11646/zootaxa.3703.1.3. - DOI - PubMed
    1. Zhang ZQ. Phylum Arthropoda. Zootaxa. 2013;3703:17–26. doi: 10.11646/zootaxa.3703.1.6. - DOI
    1. Lindquist EE. Current theories on the evolution of major groups of Acari and on their relationships with other groups of Arachnida, with consequent implications for their classificaton. In: Griffiths DA, Bowman CE. editors. Acarology VI. Volume I. Chichester: Ellis-Horwood Ltd.; 1984. p. 28–62.
    1. Krantz GW. A manual of acarology. 2. Corvallis: Oregon State University Book Stores; 1978.
    1. Walter DE, Proctor HC. Mites ecology, evolution and behaviour. Wallingford: CABI Publishing; 1999.

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