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Phenotypic variability of Leptosphaeria lindquistii (anamorph: Phoma macdonaldii), a fungal pathogen of sunflower
Growth of 17 isolates of Phoma macdonaldii, the causal agent of sunflower black stem, was investigated for response to pH and temperature, and for morphology and asexual morphogenesis (pycnidiogenesis and pycnidium size). For all isolates, the optimum pH for growth was between 4 and 5, and the optim...
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Published in: | Plant pathology 2000-04, Vol.49 (2), p.227-234 |
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description | Growth of 17 isolates of Phoma macdonaldii, the causal agent of sunflower black stem, was investigated for response to pH and temperature, and for morphology and asexual morphogenesis (pycnidiogenesis and pycnidium size). For all isolates, the optimum pH for growth was between 4 and 5, and the optimum temperature varied between 20 and 30°C and radial growth was slowest at 5 and 35°C. Significant differences in the number and size of pycnidia were observed between isolates. Pycniospore germination was investigated under various conditions in five isolates chosen for their geographical origins, pigmentation, optimum growth temperature and pycnidiogenesis. Increasing the concentration from 106 to 107 pycniospores per mL decreased the germination rate. The optimum temperature for pycniospore germination varied between 15 and 30°C, depending on the isolate, and the optimum and maximum pH values were 5 and 7, respectively. The optimum and minimum relative humidities allowing pycniospore germination were 100 and 95%, respectively. Pycniospore germination was photo‐independent. An artificial inoculation method was developed and the aggressiveness of the pathogen was assessed on a susceptible sunflower cultivar, using a 1–9 scale that integrated the percentage of necrotic area on the cotyledon petiole at the stage when the first pair of leaves was fully developed. Significant differences in aggressiveness were observed among the 17 isolates. The parameters investigated clearly suggest the occurrence of a wide phenotypic variability in Phoma macdonaldii. |
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For all isolates, the optimum pH for growth was between 4 and 5, and the optimum temperature varied between 20 and 30°C and radial growth was slowest at 5 and 35°C. Significant differences in the number and size of pycnidia were observed between isolates. Pycniospore germination was investigated under various conditions in five isolates chosen for their geographical origins, pigmentation, optimum growth temperature and pycnidiogenesis. Increasing the concentration from 106 to 107 pycniospores per mL decreased the germination rate. The optimum temperature for pycniospore germination varied between 15 and 30°C, depending on the isolate, and the optimum and maximum pH values were 5 and 7, respectively. The optimum and minimum relative humidities allowing pycniospore germination were 100 and 95%, respectively. Pycniospore germination was photo‐independent. An artificial inoculation method was developed and the aggressiveness of the pathogen was assessed on a susceptible sunflower cultivar, using a 1–9 scale that integrated the percentage of necrotic area on the cotyledon petiole at the stage when the first pair of leaves was fully developed. Significant differences in aggressiveness were observed among the 17 isolates. The parameters investigated clearly suggest the occurrence of a wide phenotypic variability in Phoma macdonaldii.</description><identifier>ISSN: 0032-0862</identifier><identifier>EISSN: 1365-3059</identifier><identifier>DOI: 10.1046/j.1365-3059.2000.00451.x</identifier><identifier>CODEN: PLPAAD</identifier><language>eng</language><publisher>Oxford, U.K. and Cambridge, USA: Blackwell Science Ltd</publisher><subject>aggressiveness ; ascospores ; asexual reproduction ; Biological and medical sciences ; black stem ; Fundamental and applied biological sciences. Psychology ; fungal anatomy ; fungal diseases of plants ; Fungal plant pathogens ; fungal spores ; geographical variation ; growth ; Helianthus annuus ; Leptosphaeria ; Life Sciences ; phenotype ; Phoma ; Phytopathology and phytopharmacy ; Phytopathology. Animal pests. Plant and forest protection ; pigmentation ; plant pathogenic fungi ; provenance ; pycnidia ; pycniospores ; spore germination ; temperature ; Variation, races, biotypes, parasitic specialization, genetics ; Vegetal Biology</subject><ispartof>Plant pathology, 2000-04, Vol.49 (2), p.227-234</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright Blackwell Science Ltd. Apr 2000</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4741-e6cc692db8dfb150a7af8aba7a4b8143fc29aa3851cd60f9fa7d0bc813de3fb53</citedby><cites>FETCH-LOGICAL-c4741-e6cc692db8dfb150a7af8aba7a4b8143fc29aa3851cd60f9fa7d0bc813de3fb53</cites><orcidid>0000-0002-4999-6975</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1391243$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02875262$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Roustaee, A</creatorcontrib><creatorcontrib>Costes, S</creatorcontrib><creatorcontrib>Dechamp-Guillaume, G</creatorcontrib><creatorcontrib>Barrault, G</creatorcontrib><title>Phenotypic variability of Leptosphaeria lindquistii (anamorph: Phoma macdonaldii), a fungal pathogen of sunflower</title><title>Plant pathology</title><description>Growth of 17 isolates of Phoma macdonaldii, the causal agent of sunflower black stem, was investigated for response to pH and temperature, and for morphology and asexual morphogenesis (pycnidiogenesis and pycnidium size). For all isolates, the optimum pH for growth was between 4 and 5, and the optimum temperature varied between 20 and 30°C and radial growth was slowest at 5 and 35°C. Significant differences in the number and size of pycnidia were observed between isolates. Pycniospore germination was investigated under various conditions in five isolates chosen for their geographical origins, pigmentation, optimum growth temperature and pycnidiogenesis. Increasing the concentration from 106 to 107 pycniospores per mL decreased the germination rate. The optimum temperature for pycniospore germination varied between 15 and 30°C, depending on the isolate, and the optimum and maximum pH values were 5 and 7, respectively. The optimum and minimum relative humidities allowing pycniospore germination were 100 and 95%, respectively. Pycniospore germination was photo‐independent. An artificial inoculation method was developed and the aggressiveness of the pathogen was assessed on a susceptible sunflower cultivar, using a 1–9 scale that integrated the percentage of necrotic area on the cotyledon petiole at the stage when the first pair of leaves was fully developed. Significant differences in aggressiveness were observed among the 17 isolates. The parameters investigated clearly suggest the occurrence of a wide phenotypic variability in Phoma macdonaldii.</description><subject>aggressiveness</subject><subject>ascospores</subject><subject>asexual reproduction</subject><subject>Biological and medical sciences</subject><subject>black stem</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>fungal anatomy</subject><subject>fungal diseases of plants</subject><subject>Fungal plant pathogens</subject><subject>fungal spores</subject><subject>geographical variation</subject><subject>growth</subject><subject>Helianthus annuus</subject><subject>Leptosphaeria</subject><subject>Life Sciences</subject><subject>phenotype</subject><subject>Phoma</subject><subject>Phytopathology and phytopharmacy</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>pigmentation</subject><subject>plant pathogenic fungi</subject><subject>provenance</subject><subject>pycnidia</subject><subject>pycniospores</subject><subject>spore germination</subject><subject>temperature</subject><subject>Variation, races, biotypes, parasitic specialization, genetics</subject><subject>Vegetal Biology</subject><issn>0032-0862</issn><issn>1365-3059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqNkVFv0zAUhSMEEmXwG7AQD0wi4dpOUgfxUk2MIVWiEuzZunHsxlUap3ayrf8eZ5nGK0_Xuv7OsXxOkhAKGYW8_HLIKC-LlENRZQwAMoC8oNnDi2T1fPEyWQFwloIo2evkTQgHAFpUlVglp12rezeeB6vIHXqLte3seCbOkK0eRheGFnVck872zWmyYbSWfMIej84P7Veya90RyRFV43rsGmsvPxMkZur32JEBx9btdT-7hak3nbvX_m3yymAX9LuneZHcXn__c3WTbn_9-Hm12aYqX-c01aVSZcWaWjSmpgXgGo3AOo68FjTnRrEKkYuCqqYEUxlcN1ArQXmjuakLfpFcLr4tdnLw9oj-LB1aebPZynkHTKwLVrI7GtkPCzt4d5p0GOXBTT5-KEhGSwFlTDJCYoGUdyF4bZ5dKci5C3mQc-RyjlzOXcjHLuRDlH588segsDMee2XDPz2vKMt5xL4t2L3t9Pm_7eVut4mHKH-_yA06iXsfX7j9zYByYFWRV3nB_wJpRqba</recordid><startdate>200004</startdate><enddate>200004</enddate><creator>Roustaee, A</creator><creator>Costes, S</creator><creator>Dechamp-Guillaume, G</creator><creator>Barrault, G</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><general>Wiley</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-4999-6975</orcidid></search><sort><creationdate>200004</creationdate><title>Phenotypic variability of Leptosphaeria lindquistii (anamorph: Phoma macdonaldii), a fungal pathogen of sunflower</title><author>Roustaee, A ; Costes, S ; Dechamp-Guillaume, G ; Barrault, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4741-e6cc692db8dfb150a7af8aba7a4b8143fc29aa3851cd60f9fa7d0bc813de3fb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>aggressiveness</topic><topic>ascospores</topic><topic>asexual reproduction</topic><topic>Biological and medical sciences</topic><topic>black stem</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>fungal anatomy</topic><topic>fungal diseases of plants</topic><topic>Fungal plant pathogens</topic><topic>fungal spores</topic><topic>geographical variation</topic><topic>growth</topic><topic>Helianthus annuus</topic><topic>Leptosphaeria</topic><topic>Life Sciences</topic><topic>phenotype</topic><topic>Phoma</topic><topic>Phytopathology and phytopharmacy</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>pigmentation</topic><topic>plant pathogenic fungi</topic><topic>provenance</topic><topic>pycnidia</topic><topic>pycniospores</topic><topic>spore germination</topic><topic>temperature</topic><topic>Variation, races, biotypes, parasitic specialization, genetics</topic><topic>Vegetal Biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roustaee, A</creatorcontrib><creatorcontrib>Costes, S</creatorcontrib><creatorcontrib>Dechamp-Guillaume, G</creatorcontrib><creatorcontrib>Barrault, G</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Plant pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roustaee, A</au><au>Costes, S</au><au>Dechamp-Guillaume, G</au><au>Barrault, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic variability of Leptosphaeria lindquistii (anamorph: Phoma macdonaldii), a fungal pathogen of sunflower</atitle><jtitle>Plant pathology</jtitle><date>2000-04</date><risdate>2000</risdate><volume>49</volume><issue>2</issue><spage>227</spage><epage>234</epage><pages>227-234</pages><issn>0032-0862</issn><eissn>1365-3059</eissn><coden>PLPAAD</coden><abstract>Growth of 17 isolates of Phoma macdonaldii, the causal agent of sunflower black stem, was investigated for response to pH and temperature, and for morphology and asexual morphogenesis (pycnidiogenesis and pycnidium size). For all isolates, the optimum pH for growth was between 4 and 5, and the optimum temperature varied between 20 and 30°C and radial growth was slowest at 5 and 35°C. Significant differences in the number and size of pycnidia were observed between isolates. Pycniospore germination was investigated under various conditions in five isolates chosen for their geographical origins, pigmentation, optimum growth temperature and pycnidiogenesis. Increasing the concentration from 106 to 107 pycniospores per mL decreased the germination rate. The optimum temperature for pycniospore germination varied between 15 and 30°C, depending on the isolate, and the optimum and maximum pH values were 5 and 7, respectively. The optimum and minimum relative humidities allowing pycniospore germination were 100 and 95%, respectively. Pycniospore germination was photo‐independent. An artificial inoculation method was developed and the aggressiveness of the pathogen was assessed on a susceptible sunflower cultivar, using a 1–9 scale that integrated the percentage of necrotic area on the cotyledon petiole at the stage when the first pair of leaves was fully developed. Significant differences in aggressiveness were observed among the 17 isolates. The parameters investigated clearly suggest the occurrence of a wide phenotypic variability in Phoma macdonaldii.</abstract><cop>Oxford, U.K. and Cambridge, USA</cop><pub>Blackwell Science Ltd</pub><doi>10.1046/j.1365-3059.2000.00451.x</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4999-6975</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | aggressiveness ascospores asexual reproduction Biological and medical sciences black stem Fundamental and applied biological sciences. Psychology fungal anatomy fungal diseases of plants Fungal plant pathogens fungal spores geographical variation growth Helianthus annuus Leptosphaeria Life Sciences phenotype Phoma Phytopathology and phytopharmacy Phytopathology. Animal pests. Plant and forest protection pigmentation plant pathogenic fungi provenance pycnidia pycniospores spore germination temperature Variation, races, biotypes, parasitic specialization, genetics Vegetal Biology |
title | Phenotypic variability of Leptosphaeria lindquistii (anamorph: Phoma macdonaldii), a fungal pathogen of sunflower |
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