The First Complete Mitochondrial Genomes of Two Sibling Species from Nitidulid Beetles Pests
1
Academy of National Food and Strategic Reserves Administration, No. 11 Baiwanzhuang Street, Beijing 100037, China
2
Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China
*
Author to whom correspondence should be addressed.
Insects 2020, 11(1), 24; https://doi.org/10.3390/insects11010024
Submission received: 12 November 2019
/
Revised: 21 December 2019
/
Accepted: 26 December 2019
/
Published: 28 December 2019
(This article belongs to the Collection Stored-Product Pests: Biology, Ecology, Behavior and Integrated Management)
Abstract
:Carpophilus dimidiatus (Fabricius, 1792) and Carpophilus pilosellus Motschulsky are two sibling species and economically important storage pests worldwide. The first complete mitochondrial (mt) genomes of both were sequenced using next-generation sequencing. The mt genomes of C. dimidiatus and C. pilosellus are circular, with total lengths of 15,717 bp and 15,686 bp, respectively. Gene order and content for both species are similar to what has been observed in ancestral insects and consist of 13 protein-coding genes, two ribosomal RNA genes, 22 transfer RNA genes, and a control region. Comparing the mt genome data of C. dimidiatus and C. pilosellus, they are similar in organization, arrangement patterns, GC contents, transfer RNA (tRNA) secondary structures, and codon usage patterns. Small differences were noted with regards to the nucleotide similarity of coding regions and the control region. This is the first publication of the complete mitochondrial genomes of two sibling species. The mt genome sequences can supplement the nuclear markers of the Carpophilus genus in research species identification, system evolution, and population genetic structure, and also will be valuable molecular marker for further genetic studies.
1. Introduction
The beetle genus Carpophilus (Coleoptera: Nitidulidae: Carpophilinae) is one cluster in taxonomic lineage. There are about 200 Carpophilus species, most of which are distributed in the tropics and subtropics [1,2,3,4]. Some species are considered important stored-product pests. Carpophilus dimidiatus (Fabricius, 1792) and Carpophilus pilosellus Motschulsky are two sibling species that show a strong preference for attacking stored grain, dry fruits, Chinese herbal medicine, and many other stored-product commodities. They reduce the quality and quantity of stored products and create conditions for the growth of molds and fungi [5,6,7]. Carpophilus dimidiatus threatens the brewing and fermentation industry, and is distributed worldwide [8,9]. Carpophilus pilosellus is often found in dry fruit storage sites and has a received widespread distribution across China, Japan, Vietnam, and India [10,11].
Very few studies focused on both C. dimidiatus and C. pilosellus have been reported, except for harm, taxonomy, and first records, in some regions and countries [1,10]. Molecular information on the two species is inadequate, with only few reports about the molecular identification C. dimidiatus by species-specific PCR and barcode fragments of mitochondrial cytochrome c oxidase I (cox1) gene [8,9]. The molecular data of storage pests are very useful, not only to study the population structure and geographical variability but also to resolve ecological and taxonomic relationships [12,13,14].
In most insects, mitochondrial (mt) genomes contain a circular chromosome and have a relatively stable structure. The mt genomes share an ancestral pattern of gene arrangement, containing 37 genes: 13 protein-coding genes (PCGs), 22 transfer RNA (tRNA) genes, and two ribosomal RNA (rRNA) genes [15,16,17]. The whole mt genome is playing an increasingly important role in intraspecific and interspecific genetic differences, phylogeographic studies, and rapid diagnostics [18,19,20]. At the time of this report, no mt genomes of Carpophilus species were reported in GenBank. In this study, we report the first complete mt genomes of C. dimidiatus and C. pilosellus, analyze the gene arrangement, and compare the mt genome data between the two sibling species. The results provide valuable nuclear markers for the further study of the genetic structure of populations and the phylogenetic analysis of nitidulid beetles.
2. Materials and Methods
2.1. Sampling and DNA Extraction
Carpophilus dimidiatus was collected from a grain processing facility at Hujian—Zhangzhou, China, in 2016, and C. pilosellus was collected from dry fruit storage sites at Hebei—Qinhuangdao, China, in 2017. All adult samples were identified by their morphology features [11]. Genomic DNA was extracted from three adults that been pooled into one centrifuge tube, using the TIANamp Micro DNA Kit (TIANGEN Biotech, Beijing, China) following manufacturer’s instructions. DNA concentrations were tested using a UV-Vis Spectrophotometer (Q5000, Quawell Technology, Inc., Sunnyvale, CA, USA).
2.2. Sequencing and Assembly
The two sequencing libraries were prepared with total DNA of C. dimidiatus and C. pilosellus, respectively. Sequencing was carried out on Illumina Hiseq2500 with 500 cycles and 250 bp paired-end sequencing at the Berry Genomics Company, Beijing, China.
A quality assessment of raw FASTQ files for the two libraries was carried using FastQCv0.11.8 (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/). The adapter sequences were removed with Trimmomatic v0.30 using the parameter LEADING:3, TRAILING:3, SLIDINGWINDOW:4:5, MINLEN:25 [21]. We applied “map to reference” strategy and mapped all cleaned reads to the “anchor”. The cox1, rrnS, and rrnL gene fragments were sequenced as the “anchor”. Illumina sequence-reads were assembled with Geneious11.0 [22]. This process was done iteratively over 100 times for each of the reference sequence in order to get the mt sequence. The results across the three references are identical for the both species. The contigs were assembled to the full circular mt sequences using the following parameters: (1) minimum overlap 50 bp and (2) minimum similarity 99%.
We sequenced cox1, rrnS, and rrnL gene fragments using universal primer pairs LCO1490–HCO2198 [23], 12SF–12SR, and 16Sar–16Sbr [24,25]. Polymerase chain reaction (PCR) amplification in final reaction volume of 25 µL included 12.5 µL of 2× Taq MasterMix (Tiangen, Beijing, China), 9.5 µL ddH2O, 1 µL of each primer (10 µM), and 1 µL genomic DNA. PCR cycler conditions were 95 °C or 3 min, followed by 35 cycles of 94 °C for 1 min, 50 °C for 1 min, and 72 °C for 1 min, with the final extension at 72 °C for 10 min. The amplicons were sequenced at the Berry Genomics Company, Beijing, China.
2.3. Gene Identification and Analyses
The protein coding genes (PCGs) and ribosome RNA (rRNA) genes were identified using the MITOS Web Server (http://mitos.bioinf.uni-leipzig.de/index.py) [26]. The “RefSeq 81 Metazoa” was selected as reference. Then, NCBI BLASTn with parameters (e-value < 0.001, identity > 90%) was applied to confirm the annotation results from last step. Transfer RNA (tRNA) genes were identified using tRNA-Scan [27] and ARWEN [28] based on secondary structures. If all 22 tRNAs were not found using this software, we alternatively found them by manual operation according to the codon and structure of tRNAs. MEGA 7.0 [29] was initiated to analyze the nucleotide composition, codon usage, and relative synonymous codon usage. Nucleotide compositional skew was calculated using the formula AT skew = A − T/A + T and GC skew = G − C/G + C. The circular maps of C. dimidiatus and C. pilosellus mt genome sequences were drawn with CG View40 [30]. The annotated mt genome sequence were deposited in GenBank with their accession number (submission ID were MN604384 and MN604383).
3. Results
3.1. Mt Genome Sequencing and Assembly
Both libraries of C. dimidiatus and C. pilosellus were sequenced on Hiseq2500. A total of 486,726 read-pairs for C. dimidiatus and 516,913 read-pairs for C. pilosellus were generated after removing the low-quality value reads (lower than Q20). Using the map to reference strategy with the cox1, rrnS, and rrnL genes as anchors, 56,246 reads were assembled for C. dimidiatus and 61,215 reads were assembled for C. pilosellus. After generating all the assembled reads, consensus sequence lengths of 16,313 bp for C. dimidiatus and 16,176 bp for C. pilosellus were generated. Finally, the repeats were detected manually to form the complete mitochondrial genome sequence.
3.2. Mt Genome Organization and Nucleotide Composition
The length of the mt genome of C. dimidiatus was 15,717 bp, and that of C. pilosellus was 15,686 bp. The sequenced mt genome was assembled into one circular contig, similar to many other insect mt genomes (Figure 1 and Table 1), containing 13 PCGs, 22 tRNA genes, two rRNA genes, and a non-coding region. Both of the two species share the same arrangements: four PCG genes (nad1, nad4, nad4l, and nad5), two rRNA genes (rrnS and rrnL), and eight tRNA genes (trnV, L1, P, H, F, Y, C, and Q) were located in the light strand, and the other genes were encoded by the heavy strand.
The symmetric nucleotide compositions of C. dimidiatus are A: 39.0%, C: 14.9%, G: 9.9%, and T: 36.2%, and of C. pilosellus are A: 39.6%, C: 13.4%, G: 9.4%, and T: 37.6%. As in mt genomes from other insect species, the nucleotide composition of the two nitidulid beetles was biased on A and T in C. dimidiatus (AT: 75.2%) and C. pilosellus (AT: 77.2%). Similarly, the mt genomes of both C. dimidiatus and C. pilosellus had positive AT-skews (0.037 and 0.026) and negative GC-skews (−0.202 and −0.175) (Table 2). The PCGs, rRNAs, and tRNAs all had positive AT skews and negative GC skews.
The total length of the intergenic sequences in C. dimidiatus was 120 bp, including one 24 bp intergenic sequence located between trnC gene and trnW gene. The mt genome of C. pilosellus had 190 bp intergenic sequences. Two intergenic sequences was longer than 20 bp. One was 23 bp, located between trnV gene and trnL gene, and the other was 109 bp, located between trnC gene and trnW gene. The other intergenic sequences were shorter than 20 bp. The total lengths of the overlapping regions in C. dimidiatus and C. pilosellus were 82 bp and 101 bp, respectively (Table 1). All the overlapping sequences of the two mt genomes ranged from 1 to 35 bp; the longest was between trnK and cox2.
3.3. Protein Coding Genes
The size of 13 PCGs of C. pilosellus was 11,124 bp, with 33 bp for stop codons. All PCGs could be translated into 3697 amino acid residues. Three types of start codons—ATA, ATT, and ATG—were used (Table 1). nad4, nad6, and atp6 genes started with ATA, while nad2, nad3, nad5, cox1, and cox2 started with ATT; other genes started with ATG. Additionally, there were three types of stop codon: TAG, T, and TAA. The nad1, nad3, cob, and atp8 genes stopped with TAG; the cox2, cox3, and nad4 genes had incomplete stop codons T; and the other genes stopped with TAA.
For C. dimidiatus, the total size of the 13 PCGs was 11,111 bp, which could be translated into 3692 amino acid residues. Start codons included four types: ATA, ATT, ATG, and ATC. The cob, cox3, atp6, and nad4l genes used ATG as the start codon, nad1 and nad6 were started with ATA, and ATC was used to start cox2 and atp8. The other genes started with ATT. For the stop codons, nad1, nad3, atp8, and cob were stopped by TAG. T was the incomplete stop codon of nad4 and cox3. Other genes ended with TAA.
Figure 2 shows a comparison of the relative synonymous codon usage (RSCU) of the two mt genomes. The two species shared the same codon families and have the similar feature of RSCU. The trnS1 codon UCN was the most commonly used. Furthermore, UUA (trnL1), UCU (trnS1), and CGA (trnR) were the top three codons used in the two mt genomes.
3.4. The tRNA and rRNA Genes
Twenty-two typical tRNAs were found in C. dimidiatus and C. pilosellus (Figure 3). The two sibling species had similar features in the tRNA and rRNA genes. Most tRNAs could be folded into the clover-leaf secondary structures, except for trnR, trnG, trnW, and trnH, which lacked the TΨ C-loop; meanwhile, trnS1 lacked the dihydorouridine (DHU) arm. Moreover, trnL1 of C. pilosellus lacked the TΨ C-loop. The number of base pairs in the 22 tRNAs ranged from 62 bp (trnL1 and trnC) to 71 bp (trnK). The size of the DHU-stem ranged from three to four. Most of the TΨ C-stems had 5 bp, while stems for six of the tRNAs (trnC, trnE, trnI, trnF, trnP, and trnT) had 4 bp and the TΨ C-stems of trnP and trnT was 6 bp. The features of tRNAs were conserved between the two genomes that were usually observed in most of insects.
The two genes encoding the ribosomal subunits were located between trnV and the control region, and between trnL1 and trnV. The two rRNA genes were 1275 bp (rrnL gene) and 789 bp (rrnS gene) for C. dimidiatus and 1268 bp (rrnL gene) and 788 bp (rrnS gene) for C. pilosellus.
4. Discussion
We compared the mt genomes of C. dimidiatus and C. pilosellus regarding GC contents, tRNA secondary structures, codon usage patterns, and intron characteristics. Most of these features were similar between the two species and the gene order, and other structural features were largely conserved. The main difference was the nucleotide similarity between the sibling species (Table 2). The coding regions for both mt genome data were 15,717 bp and 15,686 bp, with a nucleotide similarity of 86.7%. PCGs had a nucleotide similarity of 86.60%, including 1706 variable positions. The nad4l had the highest similarity (89.36%), and cox2 had the lowest similarity (76.63%). The average nucleotide similarity of all the cox genes was 83.51%, and the average similarity of the nad genes was 84.58%. According to the similarity, we can choose different mt genes to conduct intraspecific or interspecific studies. The mt genome of C. dimidiatus and C. pilosellus sequenced here was of a similar gene organization, order, and size to the published mt genome of Coleoptera stored grain pests, e.g., Cryptolestes ferrugineus (Stephens) was 15,511 bp [31] and Tribolium castaneum Herbst was 15,881 bp [32]. Here, the first two mt genome sequences for species within the genus Carpophilus were reported, and more data from other species in this genus will be needed for further research. Mt genome sequences will enable the resolution of species identification, phylogenetics studies, and molecular evolution of nitidulid beetles.
5. Conclusions
Through illumina DNA sequencing and assembly, the mt genome sequences of the two sibling species C. dimidiatus and C. pilosellus were obtained, and the coding regions were 15,717 bp and 15,686 bp, respectively. Except for the differences in nucleotide composition, they share similar organization and arrangement patterns. This study is the first description of the complete mitochondrial genome for Carpophilus species. The mt genome sequences will be important resources for further molecular studies with C. dimidiatus and C. pilosellus.
Author Contributions
Conceptualization, Y.C.; methodology, Y.L.; software, L.X.; validation, M.C., W.S., and Z.D.; formal analysis, L.X.; writing—original draft preparation, writing—review and editing, Y.W.; funding acquisition, Y.W. and Y.C. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by Optional Research Project of Academy of National Food and Strategic Reserves Administration (ZX1917-1 and ZX1917-2) and National Key R&D Program of China (2016YFD0401004-2).
Conflicts of Interest
The authors declare no conflict of interest.
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Figure 1.
The mitochondrial genome arrangements of C. dimidiatus and C. pilosellus. The yellow is protein-coding genes (PCGs), the red is rRNA genes, and the purple is transfer RNA (tRNA) genes. The AT content and GC content were plotted using a blue and green sliding window, respectively, as the deviation from the average AT content and GC content of the entire sequence.
Figure 1.
The mitochondrial genome arrangements of C. dimidiatus and C. pilosellus. The yellow is protein-coding genes (PCGs), the red is rRNA genes, and the purple is transfer RNA (tRNA) genes. The AT content and GC content were plotted using a blue and green sliding window, respectively, as the deviation from the average AT content and GC content of the entire sequence.
Figure 2.
Relative synonymous codon usage (RSCU) for the mitochondrial genomes of C. dimidiatus and C. pilosellus. Codon families are shown on the X-axis.
Figure 2.
Relative synonymous codon usage (RSCU) for the mitochondrial genomes of C. dimidiatus and C. pilosellus. Codon families are shown on the X-axis.
Figure 3.
Putative secondary structures of tRNAs found in the mitochondrial genome of C. dimidiatus (a) and C. pilosellus (b).
Figure 3.
Putative secondary structures of tRNAs found in the mitochondrial genome of C. dimidiatus (a) and C. pilosellus (b).
Table 1.
Annotation of the mitochondrial genome of Carpophilus dimidiatus and Carpophilus pilosellus.
Table 1.
Annotation of the mitochondrial genome of Carpophilus dimidiatus and Carpophilus pilosellus.
| Gene | Strand | Position | Length (bp) | Anti/Start Codon | Stop Codon | Intergenic Sequence (bp) |
|---|---|---|---|---|---|---|
| rrnS | N | 14505-15293/14565-15352 | 789/788 | 0 | ||
| trnV (tac) | N | 14436-14504/14496-14564 | 69 | 0 | ||
| rrnL | N | 13144-14418/13205-14472 | 1275/1268 | 15/23 | ||
| trnL1 (tag) | N | 13085-13146/13146-13207 | 62 | 1 | ||
| nad1 | N | 12133-13065/12195-13142 | 933/948 | ATA/ATG | TAG | 19/3 |
| trnS2 (tga) | J | 12048-12115/12110-12177 | 68 | 17 | ||
| cob | J | 10910-12049/10969-12111 | 1140/1143 | ATG | TAG | −2 |
| nad6 | J | 10404-10910/10463-10969 | 507 | ATA | TAA | −1 |
| trnP (tgg) | N | 10337-10399/10396-10458 | 63 | 4 | ||
| trnT (tgt) | J | 10273-10336/10332-10395 | 64 | 0 | ||
| nad4l | N | 9989-10270/10048-10329 | 282 | ATG | TAA | 2 |
| nad4 | N | 8669-9980/8716-10051 | 1312/1336 | ATT/ATA | T | 8/−4 |
| trnH (cac) | N | 8608-8671/8666-8730 | 64/65 | −3/−15 | ||
| nad5 | N | 6880-8592/6938-8665 | 1713/1728 | ATT | TAA | 17/0 |
| trnF (gaa) | N | 6832-6896/6891-6954 | 65/64 | −17 | ||
| trnE (ttc) | J | 6771-6833/6830-6892 | 63 | −2 | ||
| trnS1 (tct) | J | 6704-6770/6763-6829 | 67 | 0 | ||
| trnN (gtt) | J | 6640-6703/6697-6762 | 64/66 | 0 | ||
| trnR (tcg) | J | 6577-6639/6635-6697 | 63 | 0/−1 | ||
| trnA (tgc) | J | 6513-6577/6571-6635 | 65 | −1 | ||
| nad3 | J | 6161-6514/6225-6572 | 354/348 | ATT | TAG | −2 |
| trnG (tcc) | J | 6097-6160/6155-6218 | 64 | 0/6 | ||
| cox3 | J | 5310-6096/5368-6154 | 787 | ATG | T | 0 |
| atp6 | J | 4642-5310/4703-5368 | 669/666 | ATG/ATA | TAA | −1 |
| atp8 | J | 4493-4648/4551-4706 | 156 | ATC | TAG | −7/−4 |
| trnD (gtc) | J | 4427-4492/4485-4550 | 66 | 0 | ||
| trnK (ctt) | J | 4352-4422/4410-4480 | 71 | 4 | ||
| cox2 | J | 3664-4386/3722-4409 | 723/688 | ATC/ATT | TAA/T | −35 |
| trnL2 (taa) | J | 3599-3663/3657-3721 | 65 | 0 | ||
| cox1 | J | 2059-3603/2117-3661 | 1545 | ATT | TAA | 3/−5 |
| trnY (gta) | N | 2001-2066/2059-2124 | 66 | −8 | ||
| trnC (gca) | N | 1939-2000/1997-2058 | 62 | 0 | ||
| trnW (tca) | J | 1848-1914/1821-1887 | 67 | 24/109 | ||
| nad2 | J | 837-1844/828-1817 | 1008/990 | ATT | TAA | 3 |
| trnM (cat) | J | 768-836/741-809 | 69 | 0/18 | ||
| trnQ (ttg) | N | 696-764/672-740 | 69 | 3/0 | ||
| trnI (gat) | J | 634-698/611-674 | 65/64 | −3 |
Note: N and J indicates that the gene was located in the minor (N) and major (J) strand. The ‘/‘ indicates that the left was C. dimidiatus and the right was C. pilosellus. Intergenic sequence: positive numbers/negative numbers indicate intergenic/overlapping regions between adjacent genes.
Table 2.
Nucleotide composition and similarity of mitochondrial genomes of C. dimidiatus and C. pilosellus.
Table 2.
Nucleotide composition and similarity of mitochondrial genomes of C. dimidiatus and C. pilosellus.
| Feature | A + T% | AT-Skew | GC-Skew | Similarity | |||
|---|---|---|---|---|---|---|---|
| C. dimidiatus | C. pilosellus | C. dimidiatus | C. pilosellus | C. dimidiatus | C. pilosellus | ||
| Whole mt genome | 75.2 | 77.2 | 0.037 | 0.026 | −0.202 | −0.175 | 86.7 |
| PCGs | 74.3 | 76.6 | 0.039 | 0.023 | −0.191 | −0.149 | 86.6 |
| tRNA | 74.9 | 76.3 | 0.031 | 0.020 | −0.092 | −0.089 | 91.6 |
| tRNA genes | 75.0 | 78.5 | 0.091 | 0.070 | −0.373 | −0.361 | 89.6 |
| rrnL gene | 74.9 | 75.4 | 0.036 | 0.053 | −0.331 | −0.360 | 91.1 |
| rrnS gene | 75.2 | 77.2 | 0.037 | 0.026 | −0.202 | −0.175 | 86.7 |
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Wu, Y.; Lan, Y.; Xia, L.; Cui, M.; Sun, W.; Dong, Z.; Cao, Y. The First Complete Mitochondrial Genomes of Two Sibling Species from Nitidulid Beetles Pests. Insects 2020, 11, 24. https://doi.org/10.3390/insects11010024
AMA Style
Wu Y, Lan Y, Xia L, Cui M, Sun W, Dong Z, Cao Y. The First Complete Mitochondrial Genomes of Two Sibling Species from Nitidulid Beetles Pests. Insects. 2020; 11(1):24. https://doi.org/10.3390/insects11010024
Chicago/Turabian StyleWu, Yi, Yangming Lan, Liyuan Xia, Miao Cui, Weiwei Sun, Zhen Dong, and Yang Cao. 2020. "The First Complete Mitochondrial Genomes of Two Sibling Species from Nitidulid Beetles Pests" Insects 11, no. 1: 24. https://doi.org/10.3390/insects11010024
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