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Distinct Electrophoretic Isozyme Profiles of Fusarium graminearum and Closely Related Species
Cellulose-acetate electrophoresis (CAE) was used to investigate isozyme polymorphisms among different isolates of Fusarium cerealis, F. culmorum, F. graminearum and F. pseudograminearum from around the world. After initial testing of 22 enzymes in three buffer systems for activity and resolution of...
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Published in: | Systematic and applied microbiology 2001-04, Vol.24 (1), p.67-75 |
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description | Cellulose-acetate electrophoresis (CAE) was used to investigate isozyme polymorphisms among different isolates of
Fusarium cerealis, F. culmorum, F. graminearum and
F. pseudograminearum from around the world. After initial testing of 22 enzymes in three buffer systems for activity and resolution of bands, 12 proved to be appropriate for analysis of the full sample set. Remarkably uniform isozyme patterns were obtained intraspecifically, irrespective of the geographical origin of the isolates or the host/substratum from which they were isolated. This result indicated that isolates within a given species are descendant from a same ancestral population. Comparing the different electrophoretic types (ETs), adenylate kinase (AK), NADP dependent glutamate dehydrogenase (NADP GDH), peptidase B (PEP B), peptidase D (PEP D) and phosphoglucomutase (PGM) proved to be diagnostic for at least one species examined. However, only PEP D was useful alone as a marker to distinguish the four taxa studied providing a rapid and simple CAE based diagnostic protocol. Cluster analysis of band sharing coefficients grouped the isolates into four distinct groups corresponding to the 4 species studied. Isolates of
F. cerealis were clustered between those of
F. culmorum and
F. graminearum corroborating their known close relationship to both species. For common ETs, the similarity values between
F. cerealis and
F. culmorum and between
F. cerealis and
F.graminearum were the same. Furthermore, the similarity values and the resulting phenogram indicated that
F. graminearum is more closely related to
F. cerealis and
F. culmorum than to
F. pseudograminearum, thus the morphological similarity of
F. graminearum and
F. pseudograminearum does not reflect their genetic relationship. This fact supports the species status of
F. pseudograminearum. |
doi_str_mv | 10.1078/0723-2020-00009 |
format | article |
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Fusarium cerealis, F. culmorum, F. graminearum and
F. pseudograminearum from around the world. After initial testing of 22 enzymes in three buffer systems for activity and resolution of bands, 12 proved to be appropriate for analysis of the full sample set. Remarkably uniform isozyme patterns were obtained intraspecifically, irrespective of the geographical origin of the isolates or the host/substratum from which they were isolated. This result indicated that isolates within a given species are descendant from a same ancestral population. Comparing the different electrophoretic types (ETs), adenylate kinase (AK), NADP dependent glutamate dehydrogenase (NADP GDH), peptidase B (PEP B), peptidase D (PEP D) and phosphoglucomutase (PGM) proved to be diagnostic for at least one species examined. However, only PEP D was useful alone as a marker to distinguish the four taxa studied providing a rapid and simple CAE based diagnostic protocol. Cluster analysis of band sharing coefficients grouped the isolates into four distinct groups corresponding to the 4 species studied. Isolates of
F. cerealis were clustered between those of
F. culmorum and
F. graminearum corroborating their known close relationship to both species. For common ETs, the similarity values between
F. cerealis and
F. culmorum and between
F. cerealis and
F.graminearum were the same. Furthermore, the similarity values and the resulting phenogram indicated that
F. graminearum is more closely related to
F. cerealis and
F. culmorum than to
F. pseudograminearum, thus the morphological similarity of
F. graminearum and
F. pseudograminearum does not reflect their genetic relationship. This fact supports the species status of
F. pseudograminearum.</description><identifier>ISSN: 0723-2020</identifier><identifier>EISSN: 1618-0984</identifier><identifier>DOI: 10.1078/0723-2020-00009</identifier><identifier>PMID: 11403401</identifier><identifier>CODEN: SAMIDF</identifier><language>eng</language><publisher>Jena: Elsevier GmbH</publisher><subject>Biological and medical sciences ; Cellulose-acetate electrophoresis ; cereals ; Cluster Analysis ; Electrophoresis, Cellulose Acetate ; F. culmorum ; F. graminearum ; F. pseudograminearum ; Fundamental and applied biological sciences. Psychology ; Fusarium - classification ; Fusarium - enzymology ; Fusarium cerealis ; Fusarium graminearum ; Fusarium pseudograminearum ; Genic rearrangement. Recombination. Transposable element ; identification ; Isoenzymes - isolation & purification ; isozyme analysis ; Magnoliopsida - microbiology ; Microbiology ; Molecular and cellular biology ; Molecular genetics ; Mycological Typing Techniques ; Mycology ; Plant Diseases - microbiology ; Plant Proteins - isolation & purification ; Polymorphism, Genetic ; Systematics</subject><ispartof>Systematic and applied microbiology, 2001-04, Vol.24 (1), p.67-75</ispartof><rights>2001 Urban & Fischer Verlag</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-541c03e6712f96c2a23da73be678219b077a80560ffac7b28be779ece9e8ea373</citedby><cites>FETCH-LOGICAL-c404t-541c03e6712f96c2a23da73be678219b077a80560ffac7b28be779ece9e8ea373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14165392$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11403401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LADAY, Miklos</creatorcontrib><creatorcontrib>SZECSI, Arpad</creatorcontrib><title>Distinct Electrophoretic Isozyme Profiles of Fusarium graminearum and Closely Related Species</title><title>Systematic and applied microbiology</title><addtitle>Syst Appl Microbiol</addtitle><description>Cellulose-acetate electrophoresis (CAE) was used to investigate isozyme polymorphisms among different isolates of
Fusarium cerealis, F. culmorum, F. graminearum and
F. pseudograminearum from around the world. After initial testing of 22 enzymes in three buffer systems for activity and resolution of bands, 12 proved to be appropriate for analysis of the full sample set. Remarkably uniform isozyme patterns were obtained intraspecifically, irrespective of the geographical origin of the isolates or the host/substratum from which they were isolated. This result indicated that isolates within a given species are descendant from a same ancestral population. Comparing the different electrophoretic types (ETs), adenylate kinase (AK), NADP dependent glutamate dehydrogenase (NADP GDH), peptidase B (PEP B), peptidase D (PEP D) and phosphoglucomutase (PGM) proved to be diagnostic for at least one species examined. However, only PEP D was useful alone as a marker to distinguish the four taxa studied providing a rapid and simple CAE based diagnostic protocol. Cluster analysis of band sharing coefficients grouped the isolates into four distinct groups corresponding to the 4 species studied. Isolates of
F. cerealis were clustered between those of
F. culmorum and
F. graminearum corroborating their known close relationship to both species. For common ETs, the similarity values between
F. cerealis and
F. culmorum and between
F. cerealis and
F.graminearum were the same. Furthermore, the similarity values and the resulting phenogram indicated that
F. graminearum is more closely related to
F. cerealis and
F. culmorum than to
F. pseudograminearum, thus the morphological similarity of
F. graminearum and
F. pseudograminearum does not reflect their genetic relationship. This fact supports the species status of
F. pseudograminearum.</description><subject>Biological and medical sciences</subject><subject>Cellulose-acetate electrophoresis</subject><subject>cereals</subject><subject>Cluster Analysis</subject><subject>Electrophoresis, Cellulose Acetate</subject><subject>F. culmorum</subject><subject>F. graminearum</subject><subject>F. pseudograminearum</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fusarium - classification</subject><subject>Fusarium - enzymology</subject><subject>Fusarium cerealis</subject><subject>Fusarium graminearum</subject><subject>Fusarium pseudograminearum</subject><subject>Genic rearrangement. Recombination. Transposable element</subject><subject>identification</subject><subject>Isoenzymes - isolation & purification</subject><subject>isozyme analysis</subject><subject>Magnoliopsida - microbiology</subject><subject>Microbiology</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Mycological Typing Techniques</subject><subject>Mycology</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Proteins - isolation & purification</subject><subject>Polymorphism, Genetic</subject><subject>Systematics</subject><issn>0723-2020</issn><issn>1618-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQQC0EotvCmRvyBW6hM07Wjo9oaWmlSlQFjshynAkYOfFiJ0jL1-NlV_RU1ZcZzbwZjZ4Ze4XwDkG156BEXQkQUEF5-glbocS2At02T9nqf_eEneb8EwAbLfE5O0FsoG4AV-zbB59nP7mZXwRyc4rbHzHR7B2_zvHPbiR-m-LgA2UeB365ZJv8MvLvyY5-IptKbqeeb0LMFHb8joKdqeeft-Q85Rfs2WBDppfHeMa-Xl582VxVN58-Xm_e31SugWau1g06qEkqFIOWTlhR91bVXam0AnUHStkW1hKGwTrVibYjpTQ50tSSrVV9xt4e9m5T_LVQns3os6MQ7ERxyUaBRill-yiISqOQayzg-QF0KeacaDDb5EebdgbB7NWbvVyzl2v-qS8Tr4-rl26k_p4_ui7AmyNgs7NhSHZyPt9zDcp1rUXh9IGjYuy3p2RycTk56n0qX2T66B884i_7cZ2_</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>LADAY, Miklos</creator><creator>SZECSI, Arpad</creator><general>Elsevier GmbH</general><general>Elsevier</general><scope>IQODW</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>M7N</scope><scope>7X8</scope></search><sort><creationdate>20010401</creationdate><title>Distinct Electrophoretic Isozyme Profiles of Fusarium graminearum and Closely Related Species</title><author>LADAY, Miklos ; SZECSI, Arpad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-541c03e6712f96c2a23da73be678219b077a80560ffac7b28be779ece9e8ea373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>Cellulose-acetate electrophoresis</topic><topic>cereals</topic><topic>Cluster Analysis</topic><topic>Electrophoresis, Cellulose Acetate</topic><topic>F. culmorum</topic><topic>F. graminearum</topic><topic>F. pseudograminearum</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fusarium - classification</topic><topic>Fusarium - enzymology</topic><topic>Fusarium cerealis</topic><topic>Fusarium graminearum</topic><topic>Fusarium pseudograminearum</topic><topic>Genic rearrangement. Recombination. Transposable element</topic><topic>identification</topic><topic>Isoenzymes - isolation & purification</topic><topic>isozyme analysis</topic><topic>Magnoliopsida - microbiology</topic><topic>Microbiology</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Mycological Typing Techniques</topic><topic>Mycology</topic><topic>Plant Diseases - microbiology</topic><topic>Plant Proteins - isolation & purification</topic><topic>Polymorphism, Genetic</topic><topic>Systematics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LADAY, Miklos</creatorcontrib><creatorcontrib>SZECSI, Arpad</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Systematic and applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LADAY, Miklos</au><au>SZECSI, Arpad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct Electrophoretic Isozyme Profiles of Fusarium graminearum and Closely Related Species</atitle><jtitle>Systematic and applied microbiology</jtitle><addtitle>Syst Appl Microbiol</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>24</volume><issue>1</issue><spage>67</spage><epage>75</epage><pages>67-75</pages><issn>0723-2020</issn><eissn>1618-0984</eissn><coden>SAMIDF</coden><abstract>Cellulose-acetate electrophoresis (CAE) was used to investigate isozyme polymorphisms among different isolates of
Fusarium cerealis, F. culmorum, F. graminearum and
F. pseudograminearum from around the world. After initial testing of 22 enzymes in three buffer systems for activity and resolution of bands, 12 proved to be appropriate for analysis of the full sample set. Remarkably uniform isozyme patterns were obtained intraspecifically, irrespective of the geographical origin of the isolates or the host/substratum from which they were isolated. This result indicated that isolates within a given species are descendant from a same ancestral population. Comparing the different electrophoretic types (ETs), adenylate kinase (AK), NADP dependent glutamate dehydrogenase (NADP GDH), peptidase B (PEP B), peptidase D (PEP D) and phosphoglucomutase (PGM) proved to be diagnostic for at least one species examined. However, only PEP D was useful alone as a marker to distinguish the four taxa studied providing a rapid and simple CAE based diagnostic protocol. Cluster analysis of band sharing coefficients grouped the isolates into four distinct groups corresponding to the 4 species studied. Isolates of
F. cerealis were clustered between those of
F. culmorum and
F. graminearum corroborating their known close relationship to both species. For common ETs, the similarity values between
F. cerealis and
F. culmorum and between
F. cerealis and
F.graminearum were the same. Furthermore, the similarity values and the resulting phenogram indicated that
F. graminearum is more closely related to
F. cerealis and
F. culmorum than to
F. pseudograminearum, thus the morphological similarity of
F. graminearum and
F. pseudograminearum does not reflect their genetic relationship. This fact supports the species status of
F. pseudograminearum.</abstract><cop>Jena</cop><pub>Elsevier GmbH</pub><pmid>11403401</pmid><doi>10.1078/0723-2020-00009</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Cellulose-acetate electrophoresis cereals Cluster Analysis Electrophoresis, Cellulose Acetate F. culmorum F. graminearum F. pseudograminearum Fundamental and applied biological sciences. Psychology Fusarium - classification Fusarium - enzymology Fusarium cerealis Fusarium graminearum Fusarium pseudograminearum Genic rearrangement. Recombination. Transposable element identification Isoenzymes - isolation & purification isozyme analysis Magnoliopsida - microbiology Microbiology Molecular and cellular biology Molecular genetics Mycological Typing Techniques Mycology Plant Diseases - microbiology Plant Proteins - isolation & purification Polymorphism, Genetic Systematics |
title | Distinct Electrophoretic Isozyme Profiles of Fusarium graminearum and Closely Related Species |
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