Characterization of the complete mitochondrial genome of a barklouse, Lepinotus sp. (Psocodea: Trogiomorpha: Trogiidae)

Abstract Barklice in the genus Lepinotus (Psocoptera: Trogiidae) are small, soft-bodied stored-product pests that are difficult to control. We sequenced and annotated the mitochondrial (mt) genome of Lepinotus sp. The mt genome of Lepinotus sp. is 16,299 bp in size with 74.4% A + T content. The gene order was highly conserved in some of the Trogimorpha barklice. Two types of tandem repeat units were identified in CR of Lepinotus sp. The phylogenetic analysis showed that Trogiidae species was the sister group to Lepidopsocidae barklice, and the suborder Troctomorpha was polyphyletic.

Lepinotus sp. was collected from Chizhou city, Anhui Province, China in 2014 (30 66 0 N, 117 49 0 E). Voucher specimens were deposited in the Entomological Museum (Accession Number: SWU Ps-02-01-01) of the college of Plant Protection, Southwest University. Total genomic DNA was extracted using TIANamp Genomic DNA Kit (Tiangen Biotech, Beijing, China) and stored at À20 C until future use. Fragments of cox1, cytb, nad5 and 16S were amplified by PCR using conserved insect primers (Simon et al. 2006), and nad2 was derived from transcriptome data of this barklouse. Five overlapping fragments (cox1-nad5, nad5-cytb, cytb-16S, 16S-nad2 and nad2-cox1) were amplified by long PCR using the specific primers, which were designed from above-mentioned gene sequences. These fragments were assembled into contigs with SeqMan (DNAStar) and proofed manually. All products were sequenced by the Beijing Genomics Institute (BGI) at Chongqing, China.
The complete mt genome of Lepinotus sp. is a closedcircular molecule of 16,299 bp in size (GenBank accession number: MW735944), containing 13 protein-coding genes (PCGs), 22 tRNA genes, 2 rRNA genes and a control region (CR). Lepinotus sp. has the same gene arrangements and coding strand as in some published Trogimorpha barklice species, e.g. lepidopsocid sp., L. reticulatus and Dorypteryx domestica (Shao et al. 2003;Feng et al. 2018;Yoshizawa et al. 2018). The A þ T content of complete mt genome of Lepinotus sp. is 74.4% (A ¼ 38.8%, T ¼ 35.9%, C ¼ 17.9 and G ¼ 7.4%), which is similar to other reported psocids (ranging from 68.6% to 79.8%). All PCGs of Lepinotus sp. initiated with ATD (six ATT, five ATG and two ATA) as the start codons, and mostly terminated with the stop codon TAA/TAG, except for nad5 and cytb (end with the incomplete stop codon T-). The CR (1580 bp) of Lepinotus sp. is located between rrnS and trnQ, with an A þ T content of 80.0%. Two types of tandem repeat units (TR1 and TR2) were identified in CR of Lepinotus sp., and the repeat units of TR1 and TR2 were 122 bp (seven times) and 21 bp (six times) in length, respectively. Interestingly, most of the barklice possess tandem repeats in their control region, and these repeat units are highly similar among the species from the same genus, e.g. Lepinotus sp. and L. reticulatus.
The phylogenetic analysis was performed based on the nucleotide sequences of 11 PCGs (except nad6 and nad4L) and two rRNA genes (in a total length of 11,381 bp) from 20 psocids species. The mt genome sequence of Aphis citricidus was used as an outgroup (Wei et al. 2019). A GTR þ I þ G substitution model for the concatenated dataset was used as the best-fit model, which was determined by jModelTest 2.1.4 (Posada 2008). The phylogenetic tree was constructed using the maximum-likelihood (ML) method, which was performed using IQ-TREE web server with 1000 bootstrap replicates (Trifinopoulos et al. 2016). The ML tree (Figure 1) consistently supported those of previous mitochondrial phylogenetic studies (Feng et al. 2018;Yoshizawa et al. 2018). The ML tree showed that each family was recovered as a monophyletic group, and booklice (Liposcelidae) and barklice formed wellsupported mono clades, respectively. The suborder Troctomorpha was polyphyletic because the family Amphientomidae was positioned in the suborder Psocomorpha.

Disclosure statement
No potential conflict of interest was reported by the author(s).

Funding
This work was supported partially by the National Natural Science Foundation of China [31972276] and the Natural Science Foundation of Chongqing [cstc2020jcyj-msxmX0494].

Data availability statement
The data that support the findings of this study are openly available in GenBank of NCBI (https://www.ncbi.nlm.nih.gov) with an accession number of MW735944.