Literature DB >> 34926820

The complete mitochondrial genome of the Hipposideros pendleburyi (Pendlebury's leaf-nosed bat) an endemic species in Thailand.

Wasitthee Kongkachana1, Chaiwat Naktang1, Duangjai Sangsrakru1, Nukoon Jomchai1, Phuset Yingyong1, Wirulda Pootakham1, Sithichoke Tangphatsornruang1, Pipat Soisook2.   

Abstract

This study presents the first complete mitochondrial genome of the Hipposideros pendleburyi (Pendlebury's leaf-nosed bat), an endemic species in Thailand. The mitochondrial genome was 16,820 bp in length and contains 13 protein-coding genes, 2 ribosomal RNA genes, 22 transfer RNA genes, and a control region. The overall base composition was 31.5% A, 26.2% T, 28.3% C, and 14.0% G. A maximum-likelihood tree revealed that H. pendleburyi was grouped with Hipposideros armiger within the Hipposideridae clade, which has Rhinolophidae as a sister clade.
© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Hipposideros pendleburyi; Pendlebury's Leaf-nosed bat; mitochondrial genome

Year:  2021        PMID: 34926820      PMCID: PMC8676696          DOI: 10.1080/23802359.2021.2005493

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


The Pendlebury's leaf-nosed bat (Hipposideros pendleburyi) was named by Chasen in 1936 but had long been included in Hipposideros turpis (Lekagul and McNeely 1977; Corbet and Hill 1992; Francis 2008). Only a decade ago, it has been regarded as a distinct species and known only from peninsular Thailand (Soisook 2011; Thong et al. 2012). This species was found in limestone areas of seven provinces in peninsular Thailand with a colony size of up to 800 individuals (Soisook 2019). It has been assessed as a vulnerable species on the Red List of Threatened Species by IUCN, and its population size has continuously declined due to habitat disturbance by human activities and limestone quarrying (Soisook 2019). Until now, there is only one complete mitochondrial genome (Hipposideros armiger) of the bat in the family Hipposideridae available (Dong et al. 2017). The complete mitochondrial genome of H. pendleburyi provides valuable information for inferring the phylogenetic relationships of Chiroptera order and a foundation for future research. A male specimen of H. pendleburyi was collected from Tham Le Stegodon Cave, Palian District, Trang Province, Thailand (7.141 N, 99.789 E). Bat sampling in this study was permitted by the Department of National Park, Wildlife and Plant Conservation (project number 6210306). Collection and handling of bats followed the guidelines of the American Society of Mammalogists (Sikes 2016). The specimen was deposited in the Mammal Collection of the Princess Maha Chakri Sirindhorn Natural History Museum, Prince of Songkla University (PSU), Hat Yai, Songkhla, Thailand (http://www.biology.sci.psu.ac.th/pipat-soisook/, Pipat Soisook: pipat.s@psu.ac.th) under the voucher number PSUZC-MM.2021.6. Total DNA was extracted using QIAamp Tissue Kit (Qiagen, Germany). A DNA sequencing library was constructed and paired-end reads (150 bp) were sequenced by Illumina HiSeqX Ten sequencer (Illumina, Singapore). The H. pendleburyi mitochondrial genome was assembled de novo using MitoZ 2.4 (Meng et al. 2019) and annotated using the MITOS web server (Bernt et al. 2013). Protein-coding genes (PCGs) and RNA genes were confirmed using the Basic Local Alignment Search Tool (BLAST) (Altschul et al. 1990). The complete mitochondrial genome (GenBank Accession Number: MZ196220.1) was 16,820 bp in length including 13 PCGs, 2 ribosomal RNA genes (rRNAs), 22 transfer RNA genes (tRNAs), and a non-coding control region. The overall base composition was 31.5% A, 26.2% T, 28.3% C, and 14.0% G. The PCGs utilized the standard mitochondrial start codon ATN (10 with ATG, 3 with ATA) and the regular stop codons (TAA or TAG) except for cytb (AGA). The incomplete stop codon was observed in Nd4 (T–) and coxIII (TA–). Phylogenetic analysis of the H. pendleburyi mitogenome was performed based on 13 PCGs from 21 Chiroptera species and one outgroup (Mus musculus musculus). We concatenated sequences from 13 PCGs and performed multiple alignments using MUSCLE (Edgar 2004). Subsequently, amino acid replacement models were estimated using ModelTest-NG (Darriba et al. 2020) and a maximum-likelihood phylogenetic tree was constructed by RAxML-NG (Kozlov et al. 2019) with 1000 bootstrap replicates (Figure 1). The result showed that H. pendleburyi was well grouped with H. armiger within the Hipposideridae clade, which had Rhinolophidae as a sister clade. Our result is consistent with the previous study by Lei and Dong (2016).
Figure 1.

The phylogenetic relationships of H. pendleburyi and 21 Chiroptera species were inferred from maximum-likelihood analysis based on 13 PCGs. Numbers on branches represent bootstrap values.

The phylogenetic relationships of H. pendleburyi and 21 Chiroptera species were inferred from maximum-likelihood analysis based on 13 PCGs. Numbers on branches represent bootstrap values.
  9 in total

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Authors:  S F Altschul; W Gish; W Miller; E W Myers; D J Lipman
Journal:  J Mol Biol       Date:  1990-10-05       Impact factor: 5.469

2.  2016 Guidelines of the American Society of Mammalogists for the use of wild mammals in research and education.

Authors:  Robert S Sikes
Journal:  J Mammal       Date:  2016-05-28       Impact factor: 2.416

3.  MitoZ: a toolkit for animal mitochondrial genome assembly, annotation and visualization.

Authors:  Guanliang Meng; Yiyuan Li; Chentao Yang; Shanlin Liu
Journal:  Nucleic Acids Res       Date:  2019-06-20       Impact factor: 16.971

4.  MITOS: improved de novo metazoan mitochondrial genome annotation.

Authors:  Matthias Bernt; Alexander Donath; Frank Jühling; Fabian Externbrink; Catherine Florentz; Guido Fritzsch; Joern Pütz; Martin Middendorf; Peter F Stadler
Journal:  Mol Phylogenet Evol       Date:  2012-09-07       Impact factor: 4.286

5.  The Genomes of Two Bat Species with Long Constant Frequency Echolocation Calls.

Authors:  Dong Dong; Ming Lei; Panyu Hua; Yi-Hsuan Pan; Shuo Mu; Guantao Zheng; Erli Pang; Kui Lin; Shuyi Zhang
Journal:  Mol Biol Evol       Date:  2016-11-01       Impact factor: 16.240

6.  RAxML-NG: a fast, scalable and user-friendly tool for maximum likelihood phylogenetic inference.

Authors:  Alexey M Kozlov; Diego Darriba; Tomáš Flouri; Benoit Morel; Alexandros Stamatakis
Journal:  Bioinformatics       Date:  2019-11-01       Impact factor: 6.937

7.  ModelTest-NG: A New and Scalable Tool for the Selection of DNA and Protein Evolutionary Models.

Authors:  Diego Darriba; David Posada; Alexey M Kozlov; Alexandros Stamatakis; Benoit Morel; Tomas Flouri
Journal:  Mol Biol Evol       Date:  2020-01-01       Impact factor: 16.240

8.  MUSCLE: a multiple sequence alignment method with reduced time and space complexity.

Authors:  Robert C Edgar
Journal:  BMC Bioinformatics       Date:  2004-08-19       Impact factor: 3.169

9.  Phylogenomic analyses of bat subordinal relationships based on transcriptome data.

Authors:  Ming Lei; Dong Dong
Journal:  Sci Rep       Date:  2016-06-13       Impact factor: 4.379

  9 in total

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