Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species

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Main Authors: S Wickramasinghe, L Yatawara, T Agatsuma
Format: Article
Language:English
Published: Sri Lankan Society for Microbiology 2014-10-01
Series:Sri Lankan Journal of Infectious Diseases
Subjects:
Online Access:https://sljid.sljol.info/articles/6946
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author S Wickramasinghe
L Yatawara
T Agatsuma
author_facet S Wickramasinghe
L Yatawara
T Agatsuma
author_sort S Wickramasinghe
collection DOAJ
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The aims of the present study are to determine the gene order, composition, codon usage pattern, and translation initiation/termination codons of the mt genome of <em>Toxocara cani</em>s found in Sri Lanka and to compare those findings with other <em>Toxocara</em> species.</p> <p><strong> </strong></p> <p><strong>Methodology: </strong><em>Toxocara canis</em> worms used in the present study were obtained from Sri Lanka. The total genomic DNA was extracted using a part of a single worm using an Easy-DNATM Kit. PCR reactions were performed as described previously by Wickramasinghe et al., (2009). Nucleotide sequences were determined with an ABI PRISM 3100 Avant DNA sequencer using a Big Dye Terminator v3.1 Cycle Sequencing Kit. The open-reading frames and codon usage profiles of protein-coding genes were analyzed using the program DNAsis and GENETYXMAC (ver. 6.0).</p> <p><strong>Results: </strong>The partial mt genome of <em>T. canis </em>is 9611 bp in length. This partial mt genome contains 9 protein-coding genes (<em>cox</em>1-3, <em>nad</em>2-5, <em>atp</em>6 and <em>cyt</em>b), 14 transfer RNA (tRNA) genes and one ribosomal RNA gene. All genes are transcribed in the same direction as found in other members of the genus <em>Toxocara.</em> The nucleotide compositions of the obtained partial mtDNA sequences for <em>T. canis </em>is biased toward A and T, with T being the most favored nucleotide and C the least favored, in accordance with mt genomes of other nematodes. The content of A+T is 67.48% for <em>T. canis </em>(19.9% A, 47.5% T, 23.3% G and 9.3% C). The start codons we inferred in <em>T. canis</em> were ATT, GTG, ATA, GTT, TTG and ATG. Stop codons were TAG, TA and T. Six of the 8 protein genes used TAG as a translation termination codon and the other two genes (<em>atp6 and nad2</em>) used TA and T respectively. The length of 14 tRNAs is ranging from 52 bp to 68 bp and 8 more tRNAs remain to be sequenced and identified. The <em>rrnL</em> gene of <em>T. canis</em> was identified by sequence comparison with other <em>Toxocara</em> species. The <em>rrnL</em> is located between tRNA-His and <em>nad</em>3. The <em>rrnL</em> gene is 958 bp in length. A non-coding region is located between <em>nad4</em> and <em>cox1</em>. The length of this region is 112 bp in <em>T. canis.</em><strong> </strong></p> <p><strong> </strong></p> <p><strong>Conclusion: </strong>The present study determined the partial mt genome sequence of <em>T. canis</em> obtained from a dog in Sri Lanka. This study provides molecular markers for studying the systematics, population genetics and ecology of the nematodes of socioeconomic importance. Furthermore, we observed a significant difference in nucleotide length of the mitochondrial protein-coding genes, tRNAs, <em>rrnL</em> and non-coding regions of <em>T. canis</em> from three different geographical locations, Sri Lanka, China and Australia. These variations should be further investigated in future studies.<strong> </strong></p> <p><strong><em> </em></strong></p> <p><strong>Note: </strong>Nucleotide data reported in this paper is available in the GenBank<sup>TM</sup>, EMBL and DDBJ databases under the accession number <strong>JN593098</strong>.</p><p>DOI: <a href="http://dx.doi.org/10.4038/sljid.v4i2.6946">http://dx.doi.org/10.4038/sljid.v4i2.6946</a></p> <p>Sri Lankan Journal of Infectious Diseases 2014; Vol.4(2):90-98</p> <!--[if gte mso 9]><xml> <w:LatentStyles DefLockedState="false" DefUnhideWhenUsed="true" DefSemiHidden="true" DefQFormat="false" DefPriority="99" LatentStyleCount="267"> <w:LsdException Locked="false" Priority="0" SemiHidden="false" UnhideWhenUsed="false" QFormat="true" Name="Normal" /> <w:LsdException Locked="false" Priority="9" SemiHidden="false" UnhideWhenUsed="false" QFormat="true" Name="heading 1" /> <w:LsdException Locked="false" Priority="9" QFormat="true" Name="heading 2" /> <w:LsdException 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series Sri Lankan Journal of Infectious Diseases
spelling doaj.art-72a3699233154423ae06e328fba117572022-12-22T03:36:10ZengSri Lankan Society for MicrobiologySri Lankan Journal of Infectious Diseases2012-81692448-96542014-10-0142909810.4038/sljid.v4i2.69465668Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara speciesS Wickramasinghe0L Yatawara1T Agatsuma2Department of Parasitology Faculty of Medicine University of PeradeniyaDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, University of Peradeniya, Sri Lanka.Department of Environmental Health Sciences, Kochi Medical School, Oko, Nankoku City,Kochi Ken 783-8505<!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves /> <w:TrackFormatting /> <w:PunctuationKerning /> <w:ValidateAgainstSchemas /> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w:DoNotPromoteQF /> <w:LidThemeOther>EN-US</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables /> <w:SnapToGridInCell /> <w:WrapTextWithPunct /> <w:UseAsianBreakRules /> <w:DontGrowAutofit /> <w:SplitPgBreakAndParaMark /> <w:DontVertAlignCellWithSp /> <w:DontBreakConstrainedForcedTables /> <w:DontVertAlignInTxbx /> <w:Word11KerningPairs /> <w:CachedColBalance /> </w:Compatibility> <m:mathPr> <m:mathFont m:val="Cambria Math" /> <m:brkBin m:val="before" /> <m:brkBinSub m:val=" " /> <m:smallFrac m:val="off" /> <m:dispDef /> <m:lMargin m:val="0" /> <m:rMargin m:val="0" /> <m:defJc m:val="centerGroup" /> <m:wrapIndent m:val="1440" /> <m:intLim m:val="subSup" /> <m:naryLim m:val="undOvr" /> </m:mathPr></w:WordDocument> </xml><![endif]--> <p><strong>Introduction: </strong>The complete mitochondrial (mt) genomes of nematodes sequenced thus far are circular and small in length, containing 37 genes, including 12–13 protein-coding genes: namely, <em>cytochrome oxidase subunits</em> 1–3 (<em>cox</em>1–3), <em>nicotinamide adenine dinucleotide dehydrogenase subunits</em> 1–6 and 4L (<em>nad</em>1–6 and <em>nad</em>4L), <em>ATP synthase subunit</em> 6 and 8 (<em>atp</em>6 and 8), <em>cytochrome</em> b (<em>cyt</em>b), small subunit ribosomal RNA gene (<em>rrn</em>S), large subunit ribosomal RNA. The aims of the present study are to determine the gene order, composition, codon usage pattern, and translation initiation/termination codons of the mt genome of <em>Toxocara cani</em>s found in Sri Lanka and to compare those findings with other <em>Toxocara</em> species.</p> <p><strong> </strong></p> <p><strong>Methodology: </strong><em>Toxocara canis</em> worms used in the present study were obtained from Sri Lanka. The total genomic DNA was extracted using a part of a single worm using an Easy-DNATM Kit. PCR reactions were performed as described previously by Wickramasinghe et al., (2009). Nucleotide sequences were determined with an ABI PRISM 3100 Avant DNA sequencer using a Big Dye Terminator v3.1 Cycle Sequencing Kit. The open-reading frames and codon usage profiles of protein-coding genes were analyzed using the program DNAsis and GENETYXMAC (ver. 6.0).</p> <p><strong>Results: </strong>The partial mt genome of <em>T. canis </em>is 9611 bp in length. This partial mt genome contains 9 protein-coding genes (<em>cox</em>1-3, <em>nad</em>2-5, <em>atp</em>6 and <em>cyt</em>b), 14 transfer RNA (tRNA) genes and one ribosomal RNA gene. All genes are transcribed in the same direction as found in other members of the genus <em>Toxocara.</em> The nucleotide compositions of the obtained partial mtDNA sequences for <em>T. canis </em>is biased toward A and T, with T being the most favored nucleotide and C the least favored, in accordance with mt genomes of other nematodes. The content of A+T is 67.48% for <em>T. canis </em>(19.9% A, 47.5% T, 23.3% G and 9.3% C). The start codons we inferred in <em>T. canis</em> were ATT, GTG, ATA, GTT, TTG and ATG. Stop codons were TAG, TA and T. Six of the 8 protein genes used TAG as a translation termination codon and the other two genes (<em>atp6 and nad2</em>) used TA and T respectively. The length of 14 tRNAs is ranging from 52 bp to 68 bp and 8 more tRNAs remain to be sequenced and identified. The <em>rrnL</em> gene of <em>T. canis</em> was identified by sequence comparison with other <em>Toxocara</em> species. The <em>rrnL</em> is located between tRNA-His and <em>nad</em>3. The <em>rrnL</em> gene is 958 bp in length. A non-coding region is located between <em>nad4</em> and <em>cox1</em>. The length of this region is 112 bp in <em>T. canis.</em><strong> </strong></p> <p><strong> </strong></p> <p><strong>Conclusion: </strong>The present study determined the partial mt genome sequence of <em>T. canis</em> obtained from a dog in Sri Lanka. This study provides molecular markers for studying the systematics, population genetics and ecology of the nematodes of socioeconomic importance. Furthermore, we observed a significant difference in nucleotide length of the mitochondrial protein-coding genes, tRNAs, <em>rrnL</em> and non-coding regions of <em>T. canis</em> from three different geographical locations, Sri Lanka, China and Australia. These variations should be further investigated in future studies.<strong> </strong></p> <p><strong><em> </em></strong></p> <p><strong>Note: </strong>Nucleotide data reported in this paper is available in the GenBank<sup>TM</sup>, EMBL and DDBJ databases under the accession number <strong>JN593098</strong>.</p><p>DOI: <a href="http://dx.doi.org/10.4038/sljid.v4i2.6946">http://dx.doi.org/10.4038/sljid.v4i2.6946</a></p> <p>Sri Lankan Journal of Infectious Diseases 2014; Vol.4(2):90-98</p> <!--[if gte mso 9]><xml> <w:LatentStyles DefLockedState="false" DefUnhideWhenUsed="true" DefSemiHidden="true" DefQFormat="false" DefPriority="99" LatentStyleCount="267"> <w:LsdException Locked="false" Priority="0" SemiHidden="false" UnhideWhenUsed="false" QFormat="true" Name="Normal" /> <w:LsdException Locked="false" Priority="9" SemiHidden="false" UnhideWhenUsed="false" QFormat="true" Name="heading 1" /> <w:LsdException Locked="false" Priority="9" QFormat="true" Name="heading 2" /> <w:LsdException 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spellingShingle S Wickramasinghe
L Yatawara
T Agatsuma
Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
Sri Lankan Journal of Infectious Diseases
toxocara canis
mitochondrial genome
trna
ribosomal rna
protein-coding genes
gene arrangement
title Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
title_full Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
title_fullStr Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
title_full_unstemmed Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
title_short Toxocara canis (Ascaridida: Nematoda): Mitochondrial gene content, arrangement and composition compared with other Toxocara species
title_sort toxocara canis ascaridida nematoda mitochondrial gene content arrangement and composition compared with other toxocara species
topic toxocara canis
mitochondrial genome
trna
ribosomal rna
protein-coding genes
gene arrangement
url https://sljid.sljol.info/articles/6946
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