Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea
Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Ma, Zhiwei [verfasserIn] Chen, Zhixiong [verfasserIn] Wang, Weixia [verfasserIn] Wang, Kun [verfasserIn] Zhu, Tingheng [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of biosciences - Bangalore : Indian Acad. of Sciences, 1979, 45(2020), 1 vom: 08. Okt. |
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| Übergeordnetes Werk: |
volume:45 ; year:2020 ; number:1 ; day:08 ; month:10 |
| Links: |
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| DOI / URN: |
10.1007/s12038-020-00097-4 |
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| Katalog-ID: |
SPR041260155 |
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| 245 | 1 | 0 | |a Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
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| 520 | |a Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. | ||
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| 700 | 1 | |a Wang, Weixia |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Kun |e verfasserin |4 aut | |
| 700 | 1 | |a Zhu, Tingheng |e verfasserin |4 aut | |
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10.1007/s12038-020-00097-4 doi (DE-627)SPR041260155 (DE-599)SPRs12038-020-00097-4-e (SPR)s12038-020-00097-4-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl Ma, Zhiwei verfasserin aut Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 Chen, Zhixiong verfasserin aut Wang, Weixia verfasserin aut Wang, Kun verfasserin aut Zhu, Tingheng verfasserin aut Enthalten in Journal of biosciences Bangalore : Indian Acad. of Sciences, 1979 45(2020), 1 vom: 08. Okt. (DE-627)342317474 (DE-600)2071290-X 0973-7138 nnns volume:45 year:2020 number:1 day:08 month:10 https://dx.doi.org/10.1007/s12038-020-00097-4 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_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2020 1 08 10 |
| spelling |
10.1007/s12038-020-00097-4 doi (DE-627)SPR041260155 (DE-599)SPRs12038-020-00097-4-e (SPR)s12038-020-00097-4-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl Ma, Zhiwei verfasserin aut Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 Chen, Zhixiong verfasserin aut Wang, Weixia verfasserin aut Wang, Kun verfasserin aut Zhu, Tingheng verfasserin aut Enthalten in Journal of biosciences Bangalore : Indian Acad. of Sciences, 1979 45(2020), 1 vom: 08. Okt. (DE-627)342317474 (DE-600)2071290-X 0973-7138 nnns volume:45 year:2020 number:1 day:08 month:10 https://dx.doi.org/10.1007/s12038-020-00097-4 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_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2020 1 08 10 |
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10.1007/s12038-020-00097-4 doi (DE-627)SPR041260155 (DE-599)SPRs12038-020-00097-4-e (SPR)s12038-020-00097-4-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl Ma, Zhiwei verfasserin aut Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 Chen, Zhixiong verfasserin aut Wang, Weixia verfasserin aut Wang, Kun verfasserin aut Zhu, Tingheng verfasserin aut Enthalten in Journal of biosciences Bangalore : Indian Acad. of Sciences, 1979 45(2020), 1 vom: 08. Okt. (DE-627)342317474 (DE-600)2071290-X 0973-7138 nnns volume:45 year:2020 number:1 day:08 month:10 https://dx.doi.org/10.1007/s12038-020-00097-4 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_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2020 1 08 10 |
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10.1007/s12038-020-00097-4 doi (DE-627)SPR041260155 (DE-599)SPRs12038-020-00097-4-e (SPR)s12038-020-00097-4-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl Ma, Zhiwei verfasserin aut Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 Chen, Zhixiong verfasserin aut Wang, Weixia verfasserin aut Wang, Kun verfasserin aut Zhu, Tingheng verfasserin aut Enthalten in Journal of biosciences Bangalore : Indian Acad. of Sciences, 1979 45(2020), 1 vom: 08. Okt. (DE-627)342317474 (DE-600)2071290-X 0973-7138 nnns volume:45 year:2020 number:1 day:08 month:10 https://dx.doi.org/10.1007/s12038-020-00097-4 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_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2020 1 08 10 |
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10.1007/s12038-020-00097-4 doi (DE-627)SPR041260155 (DE-599)SPRs12038-020-00097-4-e (SPR)s12038-020-00097-4-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl Ma, Zhiwei verfasserin aut Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 Chen, Zhixiong verfasserin aut Wang, Weixia verfasserin aut Wang, Kun verfasserin aut Zhu, Tingheng verfasserin aut Enthalten in Journal of biosciences Bangalore : Indian Acad. of Sciences, 1979 45(2020), 1 vom: 08. Okt. (DE-627)342317474 (DE-600)2071290-X 0973-7138 nnns volume:45 year:2020 number:1 day:08 month:10 https://dx.doi.org/10.1007/s12038-020-00097-4 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_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 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_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2118 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2020 1 08 10 |
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Ma, Zhiwei @@aut@@ Chen, Zhixiong @@aut@@ Wang, Weixia @@aut@@ Wang, Kun @@aut@@ Zhu, Tingheng @@aut@@ |
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The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. 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|
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Ma, Zhiwei |
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Ma, Zhiwei ddc 570 bkl 42.00 misc growth misc pathogenicity Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
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0973-7138 |
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570 ASE 42.00 bkl Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea growth (dpeaa)DE-He213 pathogenicity (dpeaa)DE-He213 |
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ddc 570 bkl 42.00 misc growth misc pathogenicity |
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Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
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Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
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Ma, Zhiwei |
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Ma, Zhiwei Chen, Zhixiong Wang, Weixia Wang, Kun Zhu, Tingheng |
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exocyst subunit bcsec3 regulates growth, development and pathogenicity in botrytis cinerea |
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Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
| abstract |
Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. |
| abstractGer |
Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. |
| abstract_unstemmed |
Abstract Botrytis cinerea is a saprophytic plant pathogenic fungus that can infect a variety of crops and cause gray mold, which leads to huge losses worldwide. The role of exocyst in fungal pathogenicity is being revealed. In this study, homologous recombination technology was used to knock out the exocyst subunit BcSec3 of B. cinerea, and it was found that the BcSec3 subunit plays a crucial role in the growth and pathogenicity of B. cinerea. Compared with the wild-type strain B05.10, the mycelial growth ability of the BcSec3 deletion strain was reduced by up to 49.8%, the conidia production capacity of the deletion strain was severely lost, and no sclerotia was formed. The polygalacturonase, is one of plant cell wall hydrolases, whose activity in BcSec3 deletion strain was significantly reduced. In the tomato leaves infection assay in vitro, the lesion area caused by the BcSec3 deletion strain was only 20% of the wild type after 5 days of infection. Observation by light microscope showed that the morphology of BcSec3 deletion strain mycelium was significantly changed, the mycelium became thinner and deformed, and the polarity growth was not obvious. Further observation with laser confocal microscopy and transmission electron microscopy was conducted. It was found that compared with the wild type, the number of vesicles in BcSec3 deleted cells reduced and localization and distribution of vesicles changed. In mutant cell, vesicles relatively concentrated in the cytoplasm, while in wild-type cell mainly concentrated inside the cell membrane. These evidences indicate that the exocyst subunit BcSec3 plays an important role in the growth, development and pathogenicity of B. cinerea. |
| collection_details |
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| container_issue |
1 |
| title_short |
Exocyst subunit BcSec3 regulates growth, development and pathogenicity in Botrytis cinerea |
| url |
https://dx.doi.org/10.1007/s12038-020-00097-4 |
| remote_bool |
true |
| author2 |
Chen, Zhixiong Wang, Weixia Wang, Kun Zhu, Tingheng |
| author2Str |
Chen, Zhixiong Wang, Weixia Wang, Kun Zhu, Tingheng |
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| doi_str |
10.1007/s12038-020-00097-4 |
| up_date |
2024-07-03T21:06:59.983Z |
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| score |
7.3996077 |