Molecular phylogenetic studies on an unnamed bovine Babesia sp. based on small subunit ribosomal RNA gene sequences

The 18S small subunit ribosomal RNA (18S rRNA) gene of an unnamed Babesia species (designated B. U sp.) was sequenced and analyzed in an attempt to distinguish it from other Babesia species in China. The target DNA segment was amplified by polymerase chain reaction (PCR). The PCR product was ligated...

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Veröffentlicht in:Veterinary parasitology 2005-10, Vol.133 (1), p.1-6
Hauptverfasser: Luo, Jianxun, Yin, Hong, Liu, Zhijie, Yang, Dongying, Guan, Guiquan, Liu, Aihong, Ma, Miling, Dang, Shengzhi, Lu, Bingyi, Sun, Caiqin, Bai, Qi, Lu, Wenshun, Chen, Puyan
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container_title Veterinary parasitology
container_volume 133
creator Luo, Jianxun
Yin, Hong
Liu, Zhijie
Yang, Dongying
Guan, Guiquan
Liu, Aihong
Ma, Miling
Dang, Shengzhi
Lu, Bingyi
Sun, Caiqin
Bai, Qi
Lu, Wenshun
Chen, Puyan
description The 18S small subunit ribosomal RNA (18S rRNA) gene of an unnamed Babesia species (designated B. U sp.) was sequenced and analyzed in an attempt to distinguish it from other Babesia species in China. The target DNA segment was amplified by polymerase chain reaction (PCR). The PCR product was ligated to the pGEM-T Easy vector for sequencing. It was found that the length of the 18S rRNA gene of all B. U sp. Kashi 1 and B. U sp. Kashi 2 was 1699 bp and 1689 bp. Two phylogenetic trees were, respectively, inferred based on 18S rRNA sequence of the Chinese bovine Babesia isolates and all of Babesia species available in GenBank. The first tree showed that B. U sp. was situated in the branch between B. major Yili and B. bovis Shannxian, and the second tree revealed that B. U sp. was confined to the same group as B. caballi. The percent identity of B. U sp. with other Chinese Babesia species was between 74.2 and 91.8, while the percent identity between two B. U sp. isolates was 99.7. These results demonstrated that this B. U sp. is different from other Babesia species, but that two B. U sp. isolates obtained with nymphal and adultal Hyalomma anatolicum anatolicum tick belong to the same species.
doi_str_mv 10.1016/j.vetpar.2005.02.014
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U sp.) was sequenced and analyzed in an attempt to distinguish it from other Babesia species in China. The target DNA segment was amplified by polymerase chain reaction (PCR). The PCR product was ligated to the pGEM-T Easy vector for sequencing. It was found that the length of the 18S rRNA gene of all B. U sp. Kashi 1 and B. U sp. Kashi 2 was 1699 bp and 1689 bp. Two phylogenetic trees were, respectively, inferred based on 18S rRNA sequence of the Chinese bovine Babesia isolates and all of Babesia species available in GenBank. The first tree showed that B. U sp. was situated in the branch between B. major Yili and B. bovis Shannxian, and the second tree revealed that B. U sp. was confined to the same group as B. caballi. The percent identity of B. U sp. with other Chinese Babesia species was between 74.2 and 91.8, while the percent identity between two B. U sp. isolates was 99.7. These results demonstrated that this B. U sp. is different from other Babesia species, but that two B. U sp. isolates obtained with nymphal and adultal Hyalomma anatolicum anatolicum tick belong to the same species.</description><identifier>ISSN: 0304-4017</identifier><identifier>EISSN: 1873-2550</identifier><identifier>DOI: 10.1016/j.vetpar.2005.02.014</identifier><identifier>PMID: 15982821</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>18S rRNA ; Animals ; Babesia ; Babesia - genetics ; Babesia U sp ; babesiosis ; Babesiosis - parasitology ; Babesiosis - veterinary ; Base Sequence ; calves ; Cattle ; Cattle Diseases - parasitology ; China ; disease vectors ; DNA, Protozoan - chemistry ; DNA, Protozoan - genetics ; Hyalomma anatolicum anatolicum ; Ixodidae ; Molecular Sequence Data ; molecular systematics ; nucleotide sequences ; Phylogenetic relationship ; Phylogeny ; Polymerase Chain Reaction - veterinary ; ribosomal DNA ; RNA, Ribosomal, 18S - chemistry ; RNA, Ribosomal, 18S - genetics ; Sequence Alignment ; sequence homology ; ticks</subject><ispartof>Veterinary parasitology, 2005-10, Vol.133 (1), p.1-6</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-d9d002932f0be524eed357b0b6ff6253230617fbe3550b05ab9a5ea918bb65f73</citedby><cites>FETCH-LOGICAL-c415t-d9d002932f0be524eed357b0b6ff6253230617fbe3550b05ab9a5ea918bb65f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0304401705002414$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15982821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Jianxun</creatorcontrib><creatorcontrib>Yin, Hong</creatorcontrib><creatorcontrib>Liu, Zhijie</creatorcontrib><creatorcontrib>Yang, Dongying</creatorcontrib><creatorcontrib>Guan, Guiquan</creatorcontrib><creatorcontrib>Liu, Aihong</creatorcontrib><creatorcontrib>Ma, Miling</creatorcontrib><creatorcontrib>Dang, Shengzhi</creatorcontrib><creatorcontrib>Lu, Bingyi</creatorcontrib><creatorcontrib>Sun, Caiqin</creatorcontrib><creatorcontrib>Bai, Qi</creatorcontrib><creatorcontrib>Lu, Wenshun</creatorcontrib><creatorcontrib>Chen, Puyan</creatorcontrib><title>Molecular phylogenetic studies on an unnamed bovine Babesia sp. based on small subunit ribosomal RNA gene sequences</title><title>Veterinary parasitology</title><addtitle>Vet Parasitol</addtitle><description>The 18S small subunit ribosomal RNA (18S rRNA) gene of an unnamed Babesia species (designated B. U sp.) was sequenced and analyzed in an attempt to distinguish it from other Babesia species in China. The target DNA segment was amplified by polymerase chain reaction (PCR). The PCR product was ligated to the pGEM-T Easy vector for sequencing. It was found that the length of the 18S rRNA gene of all B. U sp. Kashi 1 and B. U sp. Kashi 2 was 1699 bp and 1689 bp. Two phylogenetic trees were, respectively, inferred based on 18S rRNA sequence of the Chinese bovine Babesia isolates and all of Babesia species available in GenBank. The first tree showed that B. U sp. was situated in the branch between B. major Yili and B. bovis Shannxian, and the second tree revealed that B. U sp. was confined to the same group as B. caballi. The percent identity of B. U sp. with other Chinese Babesia species was between 74.2 and 91.8, while the percent identity between two B. U sp. isolates was 99.7. These results demonstrated that this B. U sp. is different from other Babesia species, but that two B. U sp. isolates obtained with nymphal and adultal Hyalomma anatolicum anatolicum tick belong to the same species.</description><subject>18S rRNA</subject><subject>Animals</subject><subject>Babesia</subject><subject>Babesia - genetics</subject><subject>Babesia U sp</subject><subject>babesiosis</subject><subject>Babesiosis - parasitology</subject><subject>Babesiosis - veterinary</subject><subject>Base Sequence</subject><subject>calves</subject><subject>Cattle</subject><subject>Cattle Diseases - parasitology</subject><subject>China</subject><subject>disease vectors</subject><subject>DNA, Protozoan - chemistry</subject><subject>DNA, Protozoan - genetics</subject><subject>Hyalomma anatolicum anatolicum</subject><subject>Ixodidae</subject><subject>Molecular Sequence Data</subject><subject>molecular systematics</subject><subject>nucleotide sequences</subject><subject>Phylogenetic relationship</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction - veterinary</subject><subject>ribosomal DNA</subject><subject>RNA, Ribosomal, 18S - chemistry</subject><subject>RNA, Ribosomal, 18S - genetics</subject><subject>Sequence Alignment</subject><subject>sequence homology</subject><subject>ticks</subject><issn>0304-4017</issn><issn>1873-2550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P1SAUhonRONfRf2CUlbvWAxTabkxmJn4loybqrAm0pyM3vaVy2pvMv5eb3sSdrkjgOS_wPoy9FFAKEObtvjziMrtUSgBdgixBVI_YTjS1KqTW8JjtQEFVVCDqC_aMaA8AFZj6KbsQum1kI8WO0Zc4YreOLvH518MY73HCJXSclrUPSDxO3E18nSZ3wJ77eAwT8mvnkYLjNJfcO8oHGaODG0dOq1-nsPAUfKSYt_j3r1f8lMoJf684dUjP2ZPBjYQvzuslu_vw_ufNp-L228fPN1e3RVcJvRR92wPIVskBPGpZIfZK1x68GQYjtZIKjKgHjyr_1oN2vnUaXSsa740eanXJ3my5c4r5alrsIVCH4-gmjCtZ02jdQqv_C4oaTKWNyWC1gV2KRAkHO6dwcOnBCrAnK3ZvNyv2ZMWCtNlKHnt1zl99rvHv0FlDBl5vwOCidfcpkL37IUEoEKBE06hMvNsIzIUdAyZLXTi12YeE3WL7GP79hj-4nKn0</recordid><startdate>20051010</startdate><enddate>20051010</enddate><creator>Luo, Jianxun</creator><creator>Yin, Hong</creator><creator>Liu, Zhijie</creator><creator>Yang, Dongying</creator><creator>Guan, Guiquan</creator><creator>Liu, Aihong</creator><creator>Ma, Miling</creator><creator>Dang, Shengzhi</creator><creator>Lu, Bingyi</creator><creator>Sun, Caiqin</creator><creator>Bai, Qi</creator><creator>Lu, Wenshun</creator><creator>Chen, Puyan</creator><general>Elsevier B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20051010</creationdate><title>Molecular phylogenetic studies on an unnamed bovine Babesia sp. based on small subunit ribosomal RNA gene sequences</title><author>Luo, Jianxun ; Yin, Hong ; Liu, Zhijie ; Yang, Dongying ; Guan, Guiquan ; Liu, Aihong ; Ma, Miling ; Dang, Shengzhi ; Lu, Bingyi ; Sun, Caiqin ; Bai, Qi ; Lu, Wenshun ; Chen, Puyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d9d002932f0be524eed357b0b6ff6253230617fbe3550b05ab9a5ea918bb65f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>18S rRNA</topic><topic>Animals</topic><topic>Babesia</topic><topic>Babesia - genetics</topic><topic>Babesia U sp</topic><topic>babesiosis</topic><topic>Babesiosis - parasitology</topic><topic>Babesiosis - veterinary</topic><topic>Base Sequence</topic><topic>calves</topic><topic>Cattle</topic><topic>Cattle Diseases - parasitology</topic><topic>China</topic><topic>disease vectors</topic><topic>DNA, Protozoan - chemistry</topic><topic>DNA, Protozoan - genetics</topic><topic>Hyalomma anatolicum anatolicum</topic><topic>Ixodidae</topic><topic>Molecular Sequence Data</topic><topic>molecular systematics</topic><topic>nucleotide sequences</topic><topic>Phylogenetic relationship</topic><topic>Phylogeny</topic><topic>Polymerase Chain Reaction - veterinary</topic><topic>ribosomal DNA</topic><topic>RNA, Ribosomal, 18S - chemistry</topic><topic>RNA, Ribosomal, 18S - genetics</topic><topic>Sequence Alignment</topic><topic>sequence homology</topic><topic>ticks</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Jianxun</creatorcontrib><creatorcontrib>Yin, Hong</creatorcontrib><creatorcontrib>Liu, Zhijie</creatorcontrib><creatorcontrib>Yang, Dongying</creatorcontrib><creatorcontrib>Guan, Guiquan</creatorcontrib><creatorcontrib>Liu, Aihong</creatorcontrib><creatorcontrib>Ma, Miling</creatorcontrib><creatorcontrib>Dang, Shengzhi</creatorcontrib><creatorcontrib>Lu, Bingyi</creatorcontrib><creatorcontrib>Sun, Caiqin</creatorcontrib><creatorcontrib>Bai, Qi</creatorcontrib><creatorcontrib>Lu, Wenshun</creatorcontrib><creatorcontrib>Chen, Puyan</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Veterinary parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Jianxun</au><au>Yin, Hong</au><au>Liu, Zhijie</au><au>Yang, Dongying</au><au>Guan, Guiquan</au><au>Liu, Aihong</au><au>Ma, Miling</au><au>Dang, Shengzhi</au><au>Lu, Bingyi</au><au>Sun, Caiqin</au><au>Bai, Qi</au><au>Lu, Wenshun</au><au>Chen, Puyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular phylogenetic studies on an unnamed bovine Babesia sp. based on small subunit ribosomal RNA gene sequences</atitle><jtitle>Veterinary parasitology</jtitle><addtitle>Vet Parasitol</addtitle><date>2005-10-10</date><risdate>2005</risdate><volume>133</volume><issue>1</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>0304-4017</issn><eissn>1873-2550</eissn><abstract>The 18S small subunit ribosomal RNA (18S rRNA) gene of an unnamed Babesia species (designated B. U sp.) was sequenced and analyzed in an attempt to distinguish it from other Babesia species in China. The target DNA segment was amplified by polymerase chain reaction (PCR). The PCR product was ligated to the pGEM-T Easy vector for sequencing. It was found that the length of the 18S rRNA gene of all B. U sp. Kashi 1 and B. U sp. Kashi 2 was 1699 bp and 1689 bp. Two phylogenetic trees were, respectively, inferred based on 18S rRNA sequence of the Chinese bovine Babesia isolates and all of Babesia species available in GenBank. The first tree showed that B. U sp. was situated in the branch between B. major Yili and B. bovis Shannxian, and the second tree revealed that B. U sp. was confined to the same group as B. caballi. The percent identity of B. U sp. with other Chinese Babesia species was between 74.2 and 91.8, while the percent identity between two B. U sp. isolates was 99.7. These results demonstrated that this B. U sp. is different from other Babesia species, but that two B. U sp. isolates obtained with nymphal and adultal Hyalomma anatolicum anatolicum tick belong to the same species.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>15982821</pmid><doi>10.1016/j.vetpar.2005.02.014</doi><tpages>6</tpages></addata></record>
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1873-2550
language eng
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source MEDLINE; Elsevier ScienceDirect Journals
subjects 18S rRNA
Animals
Babesia
Babesia - genetics
Babesia U sp
babesiosis
Babesiosis - parasitology
Babesiosis - veterinary
Base Sequence
calves
Cattle
Cattle Diseases - parasitology
China
disease vectors
DNA, Protozoan - chemistry
DNA, Protozoan - genetics
Hyalomma anatolicum anatolicum
Ixodidae
Molecular Sequence Data
molecular systematics
nucleotide sequences
Phylogenetic relationship
Phylogeny
Polymerase Chain Reaction - veterinary
ribosomal DNA
RNA, Ribosomal, 18S - chemistry
RNA, Ribosomal, 18S - genetics
Sequence Alignment
sequence homology
ticks
title Molecular phylogenetic studies on an unnamed bovine Babesia sp. based on small subunit ribosomal RNA gene sequences
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