Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity
Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensi...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Hoffmeister, Mascha [verfasserIn] Zito, Raffaello [verfasserIn] Böhm, Jan [verfasserIn] Stammler, Gerd [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2021 |
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| Schlagwörter: |
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| Anmerkung: |
© Deutsche Phytomedizinische Gesellschaft 2021 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of plant diseases and protection - Berlin : Springer, 2006, 128(2021), 6 vom: 17. Aug., Seite 1467-1478 |
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| Übergeordnetes Werk: |
volume:128 ; year:2021 ; number:6 ; day:17 ; month:08 ; pages:1467-1478 |
| Links: |
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| DOI / URN: |
10.1007/s41348-021-00516-0 |
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| Katalog-ID: |
SPR045570442 |
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| 520 | |a Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. | ||
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10.1007/s41348-021-00516-0 doi (DE-627)SPR045570442 (SPR)s41348-021-00516-0-e DE-627 ger DE-627 rakwb eng 580 ASE 48.00 bkl Hoffmeister, Mascha verfasserin aut Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phytomedizinische Gesellschaft 2021 Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 Zito, Raffaello verfasserin aut Böhm, Jan verfasserin aut Stammler, Gerd verfasserin aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 128(2021), 6 vom: 17. Aug., Seite 1467-1478 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 https://dx.doi.org/10.1007/s41348-021-00516-0 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_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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4346 GBV_ILN_4393 GBV_ILN_4700 48.00 ASE AR 128 2021 6 17 08 1467-1478 |
| spelling |
10.1007/s41348-021-00516-0 doi (DE-627)SPR045570442 (SPR)s41348-021-00516-0-e DE-627 ger DE-627 rakwb eng 580 ASE 48.00 bkl Hoffmeister, Mascha verfasserin aut Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phytomedizinische Gesellschaft 2021 Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 Zito, Raffaello verfasserin aut Böhm, Jan verfasserin aut Stammler, Gerd verfasserin aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 128(2021), 6 vom: 17. Aug., Seite 1467-1478 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 https://dx.doi.org/10.1007/s41348-021-00516-0 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_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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4346 GBV_ILN_4393 GBV_ILN_4700 48.00 ASE AR 128 2021 6 17 08 1467-1478 |
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10.1007/s41348-021-00516-0 doi (DE-627)SPR045570442 (SPR)s41348-021-00516-0-e DE-627 ger DE-627 rakwb eng 580 ASE 48.00 bkl Hoffmeister, Mascha verfasserin aut Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phytomedizinische Gesellschaft 2021 Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 Zito, Raffaello verfasserin aut Böhm, Jan verfasserin aut Stammler, Gerd verfasserin aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 128(2021), 6 vom: 17. Aug., Seite 1467-1478 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 https://dx.doi.org/10.1007/s41348-021-00516-0 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_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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4346 GBV_ILN_4393 GBV_ILN_4700 48.00 ASE AR 128 2021 6 17 08 1467-1478 |
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10.1007/s41348-021-00516-0 doi (DE-627)SPR045570442 (SPR)s41348-021-00516-0-e DE-627 ger DE-627 rakwb eng 580 ASE 48.00 bkl Hoffmeister, Mascha verfasserin aut Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phytomedizinische Gesellschaft 2021 Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 Zito, Raffaello verfasserin aut Böhm, Jan verfasserin aut Stammler, Gerd verfasserin aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 128(2021), 6 vom: 17. Aug., Seite 1467-1478 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 https://dx.doi.org/10.1007/s41348-021-00516-0 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_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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4346 GBV_ILN_4393 GBV_ILN_4700 48.00 ASE AR 128 2021 6 17 08 1467-1478 |
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10.1007/s41348-021-00516-0 doi (DE-627)SPR045570442 (SPR)s41348-021-00516-0-e DE-627 ger DE-627 rakwb eng 580 ASE 48.00 bkl Hoffmeister, Mascha verfasserin aut Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phytomedizinische Gesellschaft 2021 Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 Zito, Raffaello verfasserin aut Böhm, Jan verfasserin aut Stammler, Gerd verfasserin aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 128(2021), 6 vom: 17. Aug., Seite 1467-1478 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 https://dx.doi.org/10.1007/s41348-021-00516-0 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_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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4346 GBV_ILN_4393 GBV_ILN_4700 48.00 ASE AR 128 2021 6 17 08 1467-1478 |
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Enthalten in Journal of plant diseases and protection 128(2021), 6 vom: 17. Aug., Seite 1467-1478 volume:128 year:2021 number:6 day:17 month:08 pages:1467-1478 |
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Apple scab Liquid cultivation method Sterol demethylation inhibitor Fungicide resistance Mefentrifluconazole |
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Hoffmeister, Mascha @@aut@@ Zito, Raffaello @@aut@@ Böhm, Jan @@aut@@ Stammler, Gerd @@aut@@ |
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They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. 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Hoffmeister, Mascha |
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Hoffmeister, Mascha ddc 580 bkl 48.00 misc Apple scab misc Liquid cultivation method misc Sterol demethylation inhibitor misc Fungicide resistance misc Mefentrifluconazole Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity |
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580 ASE 48.00 bkl Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity Apple scab (dpeaa)DE-He213 Liquid cultivation method (dpeaa)DE-He213 Sterol demethylation inhibitor (dpeaa)DE-He213 Fungicide resistance (dpeaa)DE-He213 Mefentrifluconazole (dpeaa)DE-He213 |
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ddc 580 bkl 48.00 misc Apple scab misc Liquid cultivation method misc Sterol demethylation inhibitor misc Fungicide resistance misc Mefentrifluconazole |
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mutations in cyp51 of venturia inaequalis and their effects on dmi sensitivity |
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Mutations in Cyp51 of Venturia inaequalis and their effects on DMI sensitivity |
| abstract |
Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. © Deutsche Phytomedizinische Gesellschaft 2021 |
| abstractGer |
Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. © Deutsche Phytomedizinische Gesellschaft 2021 |
| abstract_unstemmed |
Abstract DMIs (sterol demethylation inhibitors) provide an important mode of action for control of Venturia inaequalis. They target the enzyme 14a-demethylase, encoded by the Cyp51 gene, which acts on an essential precursor for ergosterol biosynthesis. One mechanism, which leads to reduced DMI sensitivity of fungi, is based on mutations in Cyp51. In contrast to other phytopathogenic fungi, only little information is available on changes in the Cyp51 gene of V. inaequalis and their potential influence on DMI sensitivity. In this study, 126 monoconidial isolates were generated from field samples of V. inaequalis collected in apple orchards in different countries in 2018 and 2019. The Cyp51 gene of all isolates was sequenced. Furthermore, a new liquid culture method for V. inaequalis was established, which provides strongly sporulating cultures as a basis for the sensitivity tests. The sequence analysis revealed 15 different point mutations, and each of them resulted in an amino acid exchange in the 14α-demethylase. For some of them, corresponding mutations had been reported in other plant pathogens and shown to influence DMI sensitivity. We measured fungal growth in microtiter-plate tests to evaluate the influence of the amino acid changes in the Cyp51 gene on the sensitivity of the isolates towards the DMIs mefentrifluconazole, difenoconazole, and myclobutanil. While some mutations (e.g. those in the YGYG region 443–446) showed little impact on DMI sensitivity, others caused higher $ EC_{50} $ values, in particular Y133F and M141T. The sensitivity reducing effects differed for the three DMIs and were most pronounced for myclobutanil and less for mefentrifluconazole. The variability in the DMI sensitivity in each Cyp51 haplotype suggests the presence of additional resistance mechanisms caused by genetic background. © Deutsche Phytomedizinische Gesellschaft 2021 |
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| score |
7.399477 |