Molecular identification of two strains of Cercospora rodmanii isolated from water hyacinth present in Yuriria lagoon, Guanajuato, Mexico and identification of new hosts for several other strains
Water hyacinth is a beautiful monocotyledon plant that has been dispersed all over the world by humans. The plant has been present in Mexico since 1907, and many water bodies have become infested with it since then. In 2001, we initiated a survey in Yuriria lagoon in southern Guanajuato state to iso...
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| Veröffentlicht in: | Fungal biology 2011-11, Vol.115 (11), p.1151-1162 |
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| creator | Montenegro-Calderón, José Guadalupe Martínez-Álvarez, José Ascención Vieyra-Hernández, Ma. Teresa Rangel-Macías, Luz Imelda Razzo-Soria, Tannia Chávez-Herrera, Roberto Ponce-Noyola, Patricia Leal-Morales, Carlos Alberto |
| description | Water hyacinth is a beautiful monocotyledon plant that has been dispersed all over the world by humans. The plant has been present in Mexico since 1907, and many water bodies have become infested with it since then. In 2001, we initiated a survey in Yuriria lagoon in southern Guanajuato state to isolate fungi able to biocontrol the plant. We isolated 25 morphologically distinct fungal cultures, of which two were identified as members of the genus
Cercospora.
Cercospora species are among the most prevalent and destructive of plant pathogens and can be found on leaves, pedicels, stems, fruits, and bracts. Only two species of
Cercospora,
Cercospora piaropi, and
Cercospora rodmanii, have been described on water hyacinth; however, the classification of these species has been controversial. Several molecular approaches have been used for
Cercospora identification, and some candidate genes have been identified for use in
Cercospora species determination. Although the nrRNA genes alone do not show sufficient resolution for species determination, histone H3, translation elongation factor1-α, β-tubulin, actin, and calmodulin have been shown in previous studies to have an adequate number of nucleotide changes to allow species identification. In the present study, we used partial sequences of the histone H3, actin, and calmodulin genes to identify our two isolates as
C. rodmanii. Our two strains are not specific to water hyacinth, as they are also pathogenic to beet and sugar beet. Similar host ranges were found for
C. rodmanii strains isolated from Tabasco in México, Zambia, and Brazil, however, the specificity for water hyacinth persists in
Cercospora piaropi Tharp and
C. rodmanii Conway, the latter being the most pathogenic.
► The nrRNA genes are not enough to identify
Cercospora to species level. ► Only actin, calmodulin and histone H3 can separate
C. rodmanii from
C. piaropi. ► From
C. rodmanii strains tested only Conway isolate is specific to water hyacinth. ►
C. piaropi is also water hyacinth specific but
C. rodmanii Conway is more virulent. ► For biocontrol purposes the specificity of an isolate must be determined. |
| doi_str_mv | 10.1016/j.funbio.2011.08.001 |
| format | Article |
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Cercospora.
Cercospora species are among the most prevalent and destructive of plant pathogens and can be found on leaves, pedicels, stems, fruits, and bracts. Only two species of
Cercospora,
Cercospora piaropi, and
Cercospora rodmanii, have been described on water hyacinth; however, the classification of these species has been controversial. Several molecular approaches have been used for
Cercospora identification, and some candidate genes have been identified for use in
Cercospora species determination. Although the nrRNA genes alone do not show sufficient resolution for species determination, histone H3, translation elongation factor1-α, β-tubulin, actin, and calmodulin have been shown in previous studies to have an adequate number of nucleotide changes to allow species identification. In the present study, we used partial sequences of the histone H3, actin, and calmodulin genes to identify our two isolates as
C. rodmanii. Our two strains are not specific to water hyacinth, as they are also pathogenic to beet and sugar beet. Similar host ranges were found for
C. rodmanii strains isolated from Tabasco in México, Zambia, and Brazil, however, the specificity for water hyacinth persists in
Cercospora piaropi Tharp and
C. rodmanii Conway, the latter being the most pathogenic.
► The nrRNA genes are not enough to identify
Cercospora to species level. ► Only actin, calmodulin and histone H3 can separate
C. rodmanii from
C. piaropi. ► From
C. rodmanii strains tested only Conway isolate is specific to water hyacinth. ►
C. piaropi is also water hyacinth specific but
C. rodmanii Conway is more virulent. ► For biocontrol purposes the specificity of an isolate must be determined.</description><identifier>ISSN: 1878-6146</identifier><identifier>EISSN: 1878-6162</identifier><identifier>DOI: 10.1016/j.funbio.2011.08.001</identifier><identifier>PMID: 22036293</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Actin ; Ascomycota - classification ; Ascomycota - genetics ; Ascomycota - isolation & purification ; Ascomycota - physiology ; beet sugar ; Biological control ; bracts ; Calcium-binding protein ; Calmodulin ; Cercospora ; Cercospora piaropi ; Classification ; Eichhornia - microbiology ; Eichhornia crassipes ; Fruits ; Fungal Proteins - genetics ; Fungi ; genes ; Histone H3 ; histones ; host range ; Host Specificity ; hosts ; Lagoons ; Leaves ; Mexico ; Molecular Sequence Data ; nrRNA ; Nucleotides ; Pathogens ; Phylogeny ; Plant Leaves - microbiology ; plant pathogens ; Stems ; sugar beet ; surface water ; surveys ; taxonomy ; translation (genetics) ; Translation elongation ; Translation elongation factor1-α ; tubulin ; β-Tubulin</subject><ispartof>Fungal biology, 2011-11, Vol.115 (11), p.1151-1162</ispartof><rights>2011 British Mycological Society</rights><rights>Copyright © 2011 British Mycological Society. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-14aff43216b10c6e461c9b3923cad96b33ad1c510a2ead6f63cf11c27afd2b4e3</citedby><cites>FETCH-LOGICAL-c483t-14aff43216b10c6e461c9b3923cad96b33ad1c510a2ead6f63cf11c27afd2b4e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.funbio.2011.08.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22036293$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Montenegro-Calderón, José Guadalupe</creatorcontrib><creatorcontrib>Martínez-Álvarez, José Ascención</creatorcontrib><creatorcontrib>Vieyra-Hernández, Ma. Teresa</creatorcontrib><creatorcontrib>Rangel-Macías, Luz Imelda</creatorcontrib><creatorcontrib>Razzo-Soria, Tannia</creatorcontrib><creatorcontrib>Chávez-Herrera, Roberto</creatorcontrib><creatorcontrib>Ponce-Noyola, Patricia</creatorcontrib><creatorcontrib>Leal-Morales, Carlos Alberto</creatorcontrib><title>Molecular identification of two strains of Cercospora rodmanii isolated from water hyacinth present in Yuriria lagoon, Guanajuato, Mexico and identification of new hosts for several other strains</title><title>Fungal biology</title><addtitle>Fungal Biol</addtitle><description>Water hyacinth is a beautiful monocotyledon plant that has been dispersed all over the world by humans. The plant has been present in Mexico since 1907, and many water bodies have become infested with it since then. In 2001, we initiated a survey in Yuriria lagoon in southern Guanajuato state to isolate fungi able to biocontrol the plant. We isolated 25 morphologically distinct fungal cultures, of which two were identified as members of the genus
Cercospora.
Cercospora species are among the most prevalent and destructive of plant pathogens and can be found on leaves, pedicels, stems, fruits, and bracts. Only two species of
Cercospora,
Cercospora piaropi, and
Cercospora rodmanii, have been described on water hyacinth; however, the classification of these species has been controversial. Several molecular approaches have been used for
Cercospora identification, and some candidate genes have been identified for use in
Cercospora species determination. Although the nrRNA genes alone do not show sufficient resolution for species determination, histone H3, translation elongation factor1-α, β-tubulin, actin, and calmodulin have been shown in previous studies to have an adequate number of nucleotide changes to allow species identification. In the present study, we used partial sequences of the histone H3, actin, and calmodulin genes to identify our two isolates as
C. rodmanii. Our two strains are not specific to water hyacinth, as they are also pathogenic to beet and sugar beet. Similar host ranges were found for
C. rodmanii strains isolated from Tabasco in México, Zambia, and Brazil, however, the specificity for water hyacinth persists in
Cercospora piaropi Tharp and
C. rodmanii Conway, the latter being the most pathogenic.
► The nrRNA genes are not enough to identify
Cercospora to species level. ► Only actin, calmodulin and histone H3 can separate
C. rodmanii from
C. piaropi. ► From
C. rodmanii strains tested only Conway isolate is specific to water hyacinth. ►
C. piaropi is also water hyacinth specific but
C. rodmanii Conway is more virulent. ► For biocontrol purposes the specificity of an isolate must be determined.</description><subject>Actin</subject><subject>Ascomycota - classification</subject><subject>Ascomycota - genetics</subject><subject>Ascomycota - isolation & purification</subject><subject>Ascomycota - physiology</subject><subject>beet sugar</subject><subject>Biological control</subject><subject>bracts</subject><subject>Calcium-binding protein</subject><subject>Calmodulin</subject><subject>Cercospora</subject><subject>Cercospora piaropi</subject><subject>Classification</subject><subject>Eichhornia - microbiology</subject><subject>Eichhornia crassipes</subject><subject>Fruits</subject><subject>Fungal Proteins - genetics</subject><subject>Fungi</subject><subject>genes</subject><subject>Histone H3</subject><subject>histones</subject><subject>host range</subject><subject>Host Specificity</subject><subject>hosts</subject><subject>Lagoons</subject><subject>Leaves</subject><subject>Mexico</subject><subject>Molecular Sequence Data</subject><subject>nrRNA</subject><subject>Nucleotides</subject><subject>Pathogens</subject><subject>Phylogeny</subject><subject>Plant Leaves - microbiology</subject><subject>plant pathogens</subject><subject>Stems</subject><subject>sugar beet</subject><subject>surface water</subject><subject>surveys</subject><subject>taxonomy</subject><subject>translation (genetics)</subject><subject>Translation elongation</subject><subject>Translation elongation factor1-α</subject><subject>tubulin</subject><subject>β-Tubulin</subject><issn>1878-6146</issn><issn>1878-6162</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks9uEzEQxlcIRKvSN0DgG5cm-F-d3QsSiqAgteIAPXCyZr3jxtHGE2xvQ5-PF8NRQk8I4YtnpN9888mfm-al4HPBhXm7nvsp9oHmkgsx5-2cc_GkORXtop0ZYeTTx1qbk-Y85zWvRwnVdovnzYmUXBnZqdPm1w2N6KYREgsDxhJ8cFACRUaelR2xXBKEmPftEpOjvKUELNGwgRgCC5lGKDgwn2jDdrVMbPUALsSyYtuEuWqyENn3KYUUgI1wRxQv2NUEEdYTFLpgN_gzOGIQh794iLhjK8olM0-JZbzHBCOjsqqLjt5eNM88jBnPj_dZc_vxw7flp9n1l6vPy_fXM6dbVWZCg_daSWF6wZ1BbYTretVJ5WDoTK8UDMJdCg4SYTDeKOeFcHIBfpC9RnXWvDnobhP9mDAXuwnZ4ThCRJqy7bjWXcs78x-kUNy0WlVSH0iXKOeE3m5T2EB6sILbfdR2bQ9R233Ulre2Rl3HXh0XTP0Gh8ehP8FW4PUB8EAW7lLI9vZrVdD1G1xyvZCVeHcgsD7ZfcBkswsYHQ4hoSt2oPBvD78BRnzKiw</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Montenegro-Calderón, José Guadalupe</creator><creator>Martínez-Álvarez, José Ascención</creator><creator>Vieyra-Hernández, Ma. Teresa</creator><creator>Rangel-Macías, Luz Imelda</creator><creator>Razzo-Soria, Tannia</creator><creator>Chávez-Herrera, Roberto</creator><creator>Ponce-Noyola, Patricia</creator><creator>Leal-Morales, Carlos Alberto</creator><general>Elsevier Ltd</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>7X8</scope><scope>M7N</scope></search><sort><creationdate>20111101</creationdate><title>Molecular identification of two strains of Cercospora rodmanii isolated from water hyacinth present in Yuriria lagoon, Guanajuato, Mexico and identification of new hosts for several other strains</title><author>Montenegro-Calderón, José Guadalupe ; Martínez-Álvarez, José Ascención ; Vieyra-Hernández, Ma. Teresa ; Rangel-Macías, Luz Imelda ; Razzo-Soria, Tannia ; Chávez-Herrera, Roberto ; Ponce-Noyola, Patricia ; Leal-Morales, Carlos Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-14aff43216b10c6e461c9b3923cad96b33ad1c510a2ead6f63cf11c27afd2b4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Actin</topic><topic>Ascomycota - classification</topic><topic>Ascomycota - genetics</topic><topic>Ascomycota - isolation & purification</topic><topic>Ascomycota - physiology</topic><topic>beet sugar</topic><topic>Biological control</topic><topic>bracts</topic><topic>Calcium-binding protein</topic><topic>Calmodulin</topic><topic>Cercospora</topic><topic>Cercospora piaropi</topic><topic>Classification</topic><topic>Eichhornia - microbiology</topic><topic>Eichhornia crassipes</topic><topic>Fruits</topic><topic>Fungal Proteins - genetics</topic><topic>Fungi</topic><topic>genes</topic><topic>Histone H3</topic><topic>histones</topic><topic>host range</topic><topic>Host Specificity</topic><topic>hosts</topic><topic>Lagoons</topic><topic>Leaves</topic><topic>Mexico</topic><topic>Molecular Sequence Data</topic><topic>nrRNA</topic><topic>Nucleotides</topic><topic>Pathogens</topic><topic>Phylogeny</topic><topic>Plant Leaves - microbiology</topic><topic>plant pathogens</topic><topic>Stems</topic><topic>sugar beet</topic><topic>surface water</topic><topic>surveys</topic><topic>taxonomy</topic><topic>translation (genetics)</topic><topic>Translation elongation</topic><topic>Translation elongation factor1-α</topic><topic>tubulin</topic><topic>β-Tubulin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montenegro-Calderón, José Guadalupe</creatorcontrib><creatorcontrib>Martínez-Álvarez, José Ascención</creatorcontrib><creatorcontrib>Vieyra-Hernández, Ma. Teresa</creatorcontrib><creatorcontrib>Rangel-Macías, Luz Imelda</creatorcontrib><creatorcontrib>Razzo-Soria, Tannia</creatorcontrib><creatorcontrib>Chávez-Herrera, Roberto</creatorcontrib><creatorcontrib>Ponce-Noyola, Patricia</creatorcontrib><creatorcontrib>Leal-Morales, Carlos Alberto</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>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Fungal biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montenegro-Calderón, José Guadalupe</au><au>Martínez-Álvarez, José Ascención</au><au>Vieyra-Hernández, Ma. Teresa</au><au>Rangel-Macías, Luz Imelda</au><au>Razzo-Soria, Tannia</au><au>Chávez-Herrera, Roberto</au><au>Ponce-Noyola, Patricia</au><au>Leal-Morales, Carlos Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular identification of two strains of Cercospora rodmanii isolated from water hyacinth present in Yuriria lagoon, Guanajuato, Mexico and identification of new hosts for several other strains</atitle><jtitle>Fungal biology</jtitle><addtitle>Fungal Biol</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>115</volume><issue>11</issue><spage>1151</spage><epage>1162</epage><pages>1151-1162</pages><issn>1878-6146</issn><eissn>1878-6162</eissn><abstract>Water hyacinth is a beautiful monocotyledon plant that has been dispersed all over the world by humans. The plant has been present in Mexico since 1907, and many water bodies have become infested with it since then. In 2001, we initiated a survey in Yuriria lagoon in southern Guanajuato state to isolate fungi able to biocontrol the plant. We isolated 25 morphologically distinct fungal cultures, of which two were identified as members of the genus
Cercospora.
Cercospora species are among the most prevalent and destructive of plant pathogens and can be found on leaves, pedicels, stems, fruits, and bracts. Only two species of
Cercospora,
Cercospora piaropi, and
Cercospora rodmanii, have been described on water hyacinth; however, the classification of these species has been controversial. Several molecular approaches have been used for
Cercospora identification, and some candidate genes have been identified for use in
Cercospora species determination. Although the nrRNA genes alone do not show sufficient resolution for species determination, histone H3, translation elongation factor1-α, β-tubulin, actin, and calmodulin have been shown in previous studies to have an adequate number of nucleotide changes to allow species identification. In the present study, we used partial sequences of the histone H3, actin, and calmodulin genes to identify our two isolates as
C. rodmanii. Our two strains are not specific to water hyacinth, as they are also pathogenic to beet and sugar beet. Similar host ranges were found for
C. rodmanii strains isolated from Tabasco in México, Zambia, and Brazil, however, the specificity for water hyacinth persists in
Cercospora piaropi Tharp and
C. rodmanii Conway, the latter being the most pathogenic.
► The nrRNA genes are not enough to identify
Cercospora to species level. ► Only actin, calmodulin and histone H3 can separate
C. rodmanii from
C. piaropi. ► From
C. rodmanii strains tested only Conway isolate is specific to water hyacinth. ►
C. piaropi is also water hyacinth specific but
C. rodmanii Conway is more virulent. ► For biocontrol purposes the specificity of an isolate must be determined.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>22036293</pmid><doi>10.1016/j.funbio.2011.08.001</doi><tpages>12</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1878-6146 |
| ispartof | Fungal biology, 2011-11, Vol.115 (11), p.1151-1162 |
| issn | 1878-6146 1878-6162 |
| language | eng |
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| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | Actin Ascomycota - classification Ascomycota - genetics Ascomycota - isolation & purification Ascomycota - physiology beet sugar Biological control bracts Calcium-binding protein Calmodulin Cercospora Cercospora piaropi Classification Eichhornia - microbiology Eichhornia crassipes Fruits Fungal Proteins - genetics Fungi genes Histone H3 histones host range Host Specificity hosts Lagoons Leaves Mexico Molecular Sequence Data nrRNA Nucleotides Pathogens Phylogeny Plant Leaves - microbiology plant pathogens Stems sugar beet surface water surveys taxonomy translation (genetics) Translation elongation Translation elongation factor1-α tubulin β-Tubulin |
| title | Molecular identification of two strains of Cercospora rodmanii isolated from water hyacinth present in Yuriria lagoon, Guanajuato, Mexico and identification of new hosts for several other strains |
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