The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species
Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fro...
Ausführliche Beschreibung
Autor*in: |
Liu, Gang [verfasserIn] Li, Qingyue [verfasserIn] Wang, Chong [verfasserIn] Xu, Caoling [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2019 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Parasitology research - Berlin : Springer, 1928, 118(2019), 4 vom: 18. Feb., Seite 1299-1306 |
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Übergeordnetes Werk: |
volume:118 ; year:2019 ; number:4 ; day:18 ; month:02 ; pages:1299-1306 |
Links: |
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DOI / URN: |
10.1007/s00436-019-06252-7 |
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Katalog-ID: |
SPR005956544 |
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100 | 1 | |a Liu, Gang |e verfasserin |4 aut | |
245 | 1 | 4 | |a The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
264 | 1 | |c 2019 | |
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520 | |a Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. | ||
650 | 4 | |a Mitochondrial DNA |7 (dpeaa)DE-He213 | |
650 | 4 | |a Coccidiosis |7 (dpeaa)DE-He213 | |
650 | 4 | |a Phylogenetic relationship |7 (dpeaa)DE-He213 | |
700 | 1 | |a Li, Qingyue |e verfasserin |4 aut | |
700 | 1 | |a Wang, Chong |e verfasserin |4 aut | |
700 | 1 | |a Xu, Caoling |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Parasitology research |d Berlin : Springer, 1928 |g 118(2019), 4 vom: 18. Feb., Seite 1299-1306 |w (DE-627)254638627 |w (DE-600)1462976-8 |x 1432-1955 |7 nnns |
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912 | |a GBV_ILN_2014 | ||
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912 | |a GBV_ILN_2021 | ||
912 | |a GBV_ILN_2025 | ||
912 | |a GBV_ILN_2026 | ||
912 | |a GBV_ILN_2027 | ||
912 | |a GBV_ILN_2031 | ||
912 | |a GBV_ILN_2034 | ||
912 | |a GBV_ILN_2037 | ||
912 | |a GBV_ILN_2038 | ||
912 | |a GBV_ILN_2039 | ||
912 | |a GBV_ILN_2044 | ||
912 | |a GBV_ILN_2048 | ||
912 | |a GBV_ILN_2049 | ||
912 | |a GBV_ILN_2050 | ||
912 | |a GBV_ILN_2055 | ||
912 | |a GBV_ILN_2057 | ||
912 | |a GBV_ILN_2059 | ||
912 | |a GBV_ILN_2061 | ||
912 | |a GBV_ILN_2064 | ||
912 | |a GBV_ILN_2065 | ||
912 | |a GBV_ILN_2068 | ||
912 | |a GBV_ILN_2070 | ||
912 | |a GBV_ILN_2086 | ||
912 | |a GBV_ILN_2088 | ||
912 | |a GBV_ILN_2093 | ||
912 | |a GBV_ILN_2106 | ||
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912 | |a GBV_ILN_2111 | ||
912 | |a GBV_ILN_2112 | ||
912 | |a GBV_ILN_2113 | ||
912 | |a GBV_ILN_2116 | ||
912 | |a GBV_ILN_2118 | ||
912 | |a GBV_ILN_2119 | ||
912 | |a GBV_ILN_2122 | ||
912 | |a GBV_ILN_2129 | ||
912 | |a GBV_ILN_2143 | ||
912 | |a GBV_ILN_2144 | ||
912 | |a GBV_ILN_2147 | ||
912 | |a GBV_ILN_2148 | ||
912 | |a GBV_ILN_2152 | ||
912 | |a GBV_ILN_2153 | ||
912 | |a GBV_ILN_2188 | ||
912 | |a GBV_ILN_2190 | ||
912 | |a GBV_ILN_2232 | ||
912 | |a GBV_ILN_2336 | ||
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912 | |a GBV_ILN_2507 | ||
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912 | |a GBV_ILN_4325 | ||
912 | |a GBV_ILN_4326 | ||
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allfields |
10.1007/s00436-019-06252-7 doi (DE-627)SPR005956544 (SPR)s00436-019-06252-7-e DE-627 ger DE-627 rakwb eng 590 610 ASE 44.44 bkl 42.00 bkl Liu, Gang verfasserin aut The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 Li, Qingyue verfasserin aut Wang, Chong verfasserin aut Xu, Caoling verfasserin aut Enthalten in Parasitology research Berlin : Springer, 1928 118(2019), 4 vom: 18. Feb., Seite 1299-1306 (DE-627)254638627 (DE-600)1462976-8 1432-1955 nnns volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 https://dx.doi.org/10.1007/s00436-019-06252-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.44 ASE 42.00 ASE AR 118 2019 4 18 02 1299-1306 |
spelling |
10.1007/s00436-019-06252-7 doi (DE-627)SPR005956544 (SPR)s00436-019-06252-7-e DE-627 ger DE-627 rakwb eng 590 610 ASE 44.44 bkl 42.00 bkl Liu, Gang verfasserin aut The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 Li, Qingyue verfasserin aut Wang, Chong verfasserin aut Xu, Caoling verfasserin aut Enthalten in Parasitology research Berlin : Springer, 1928 118(2019), 4 vom: 18. Feb., Seite 1299-1306 (DE-627)254638627 (DE-600)1462976-8 1432-1955 nnns volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 https://dx.doi.org/10.1007/s00436-019-06252-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.44 ASE 42.00 ASE AR 118 2019 4 18 02 1299-1306 |
allfields_unstemmed |
10.1007/s00436-019-06252-7 doi (DE-627)SPR005956544 (SPR)s00436-019-06252-7-e DE-627 ger DE-627 rakwb eng 590 610 ASE 44.44 bkl 42.00 bkl Liu, Gang verfasserin aut The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 Li, Qingyue verfasserin aut Wang, Chong verfasserin aut Xu, Caoling verfasserin aut Enthalten in Parasitology research Berlin : Springer, 1928 118(2019), 4 vom: 18. Feb., Seite 1299-1306 (DE-627)254638627 (DE-600)1462976-8 1432-1955 nnns volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 https://dx.doi.org/10.1007/s00436-019-06252-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.44 ASE 42.00 ASE AR 118 2019 4 18 02 1299-1306 |
allfieldsGer |
10.1007/s00436-019-06252-7 doi (DE-627)SPR005956544 (SPR)s00436-019-06252-7-e DE-627 ger DE-627 rakwb eng 590 610 ASE 44.44 bkl 42.00 bkl Liu, Gang verfasserin aut The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 Li, Qingyue verfasserin aut Wang, Chong verfasserin aut Xu, Caoling verfasserin aut Enthalten in Parasitology research Berlin : Springer, 1928 118(2019), 4 vom: 18. Feb., Seite 1299-1306 (DE-627)254638627 (DE-600)1462976-8 1432-1955 nnns volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 https://dx.doi.org/10.1007/s00436-019-06252-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.44 ASE 42.00 ASE AR 118 2019 4 18 02 1299-1306 |
allfieldsSound |
10.1007/s00436-019-06252-7 doi (DE-627)SPR005956544 (SPR)s00436-019-06252-7-e DE-627 ger DE-627 rakwb eng 590 610 ASE 44.44 bkl 42.00 bkl Liu, Gang verfasserin aut The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 Li, Qingyue verfasserin aut Wang, Chong verfasserin aut Xu, Caoling verfasserin aut Enthalten in Parasitology research Berlin : Springer, 1928 118(2019), 4 vom: 18. Feb., Seite 1299-1306 (DE-627)254638627 (DE-600)1462976-8 1432-1955 nnns volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 https://dx.doi.org/10.1007/s00436-019-06252-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.44 ASE 42.00 ASE AR 118 2019 4 18 02 1299-1306 |
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Enthalten in Parasitology research 118(2019), 4 vom: 18. Feb., Seite 1299-1306 volume:118 year:2019 number:4 day:18 month:02 pages:1299-1306 |
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Liu, Gang @@aut@@ Li, Qingyue @@aut@@ Wang, Chong @@aut@@ Xu, Caoling @@aut@@ |
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It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. 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author |
Liu, Gang |
spellingShingle |
Liu, Gang ddc 590 bkl 44.44 bkl 42.00 misc Mitochondrial DNA misc Coccidiosis misc Phylogenetic relationship The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
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590 610 ASE 44.44 bkl 42.00 bkl The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species Mitochondrial DNA (dpeaa)DE-He213 Coccidiosis (dpeaa)DE-He213 Phylogenetic relationship (dpeaa)DE-He213 |
topic |
ddc 590 bkl 44.44 bkl 42.00 misc Mitochondrial DNA misc Coccidiosis misc Phylogenetic relationship |
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ddc 590 bkl 44.44 bkl 42.00 misc Mitochondrial DNA misc Coccidiosis misc Phylogenetic relationship |
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title |
The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
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The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
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Liu, Gang |
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Liu, Gang Li, Qingyue Wang, Chong Xu, Caoling |
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complete mitochondrial genome of eimeria anseris from the wintering greater white-fronted goose in shengjin lake, china, and phylogenetic relationships among eimeria species |
title_auth |
The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
abstract |
Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. |
abstractGer |
Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. |
abstract_unstemmed |
Abstract Coccidiosis is recognized as one of the most widespread and pathogenic parasitic infections in migratory waterfowl throughout the world. It can be caused by several species of Eimeria. We sequenced the complete mitochondrial genome (mtDNA) of Eimeria anseris from wintering greater white-fronted geese (Anser albifrons) in China. The complete E. anseris mtDNA is 6179 bp in size and contains three protein-coding genes (CYT B, COI, and COIII), 12 gene fragments for large subunit ribosomal RNA (rRNA), and seven gene fragments for small subunit rRNA, but no transfer RNA genes. Available complete Eimeria mtDNA sequences are highly conserved in sequence: the sequences are all similar in length; with the same three protein-coding genes and fragmented rRNA genes; ATG is generally the start codon, and TAA and TAG are the most frequently used stop codons. Our molecular phylogenetic analyses show some species clustering into host-specific clades, but many species do not follow clear coevolutionary host segregating patterns. The results suggest that Eimeria spp. from turkeys and chickens are paraphyletic groups, while Eimeria species isolated from rabbits are a monophyletic group. E. anseris, which infects A. albifrons, and another group of Eimeria isolated from chickens form a closely related monophyletic clade. |
collection_details |
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container_issue |
4 |
title_short |
The complete mitochondrial genome of Eimeria anseris from the wintering greater white-fronted goose in Shengjin Lake, China, and phylogenetic relationships among Eimeria species |
url |
https://dx.doi.org/10.1007/s00436-019-06252-7 |
remote_bool |
true |
author2 |
Li, Qingyue Wang, Chong Xu, Caoling |
author2Str |
Li, Qingyue Wang, Chong Xu, Caoling |
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254638627 |
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c |
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doi_str |
10.1007/s00436-019-06252-7 |
up_date |
2024-07-03T19:52:56.584Z |
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1803588863615041536 |
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score |
7.399312 |