Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans
- Autores
- Southwell, Manuela; Junco, Milagros; Fernández, Alicia Silvina; Bernat, Gisele Anahí; Zegbi, Sara; Guerrero, Ines; Sagüés, María Federica
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Duddingtonia flagrans is a microfungus used for the biological control of gastrointestinal nematodes in ruminants, which negatively impacts livestock production. This study aimed to evaluate chlamydospore production in different culture media and assess its impact on nematode predatory capacity. D. flagrans was cultured in enriched Glucose Sabouraud Agar (GSA-E) with the addition of meso-inositol (MI) and mannitol (M) at different concentrations: GSA-E+MI1.1%+M2%, GSA-E+MI1.1%+M5%, GSA-E+MI2%+M2%, GSA-E+MI2%M5% and GSA only (control). Twelve plates per concentration were incubated for 3, 4, and 5 weeks, respectively, at 27±0.5°C and 70±5% RH. Chlamydospores were quantified under optical microscope after mycelium homogenization. Nematophagous activity was assessed in faecal cultures with faeces from naturally parasitised sheep, incubated for 15 days at 24ºC. Infective larvae (L3) were recovered by baermannisation, quantified, and their reduction was calculated. Data were expressed as mean ±SEM. Normality was evaluated using the Shapiro-Wilk test. Group comparisons were performed using One-Way ANOVA and Dunnett’s tests or Kruskal-Wallis and Dunn’s tests. At 3, 4, and 5 weeks, respectively, the values were: GSA: 8.4×10⁶ (±1.1×10⁶), 8.2×10⁶ (±1.4×10⁶), 8.9×10⁶ (±1.2×10⁶); GSA-E+MI1.1%+M2%: 2.9×10⁷ (±4.8×106), 3.5×10⁷ (±3.4×106), 2.6×10⁷ (±4.3×106); GSA-E+MI1.1%+M5%: 3.2×10⁷ (±3.6×106), 8.7×10⁶ (±3.0×10⁶), 2.6×10⁷ (±6.6×106); GSA-E+MI2%+M2%: 8.9×10⁶ (±3.6×10⁶), 5.4×10⁶ (±1.6×10⁶), 1.7×10⁷ (±5.2×106); GSA-E+MI2%+M5%: 1.7×10⁷ (±5.9×106), 4.1×10⁷ (±8.6×106), 6.9×10⁷ (±1.3×10⁷). The GSA-E+MI2%+M5% medium optimised chlamydospore production at 5 weeks. The numbers of L3 recovered from MI- and M-enriched media were 74-99.7% (p<0.05) lower than in the control group. Supplementation with MI and M enhances chlamydospore production of D. flagrans without compromising its predatory capacity, thus optimising its production to use it in biological control against nematodes.
Fil: Southwell, Manuela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Junco, Milagros. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Fernández, Alicia Silvina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Bernat, Gisele Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Zegbi, Sara. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Guerrero, Ines. Universidad Nacional del Centro de la Provincia de Buenos Aires. Facultad de Ciencias Veterinarias. Departamento de Sanidad Animal y Medicina Preventiva. Área Parasitología y Enfermedades Parasitarias; Argentina
Fil: Sagüés, María Federica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
30th Conference of the World Association for the Advancement of Veterinary Parasitology
Curitiba
Brasil
World Association for the Advancement of Veterinary Parasitology - Materia
-
OPTIMISED CULTURE MEDIA
MESO-INOSITOL
MANNITOL
CHLAMYDOSPORES
DUDDINGTONIA FLAGRANS
BIOLOGICAL CONTROL
GASTROINTESTINAL NEMATODES - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/280025
Ver los metadatos del registro completo
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Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagransSouthwell, ManuelaJunco, MilagrosFernández, Alicia SilvinaBernat, Gisele AnahíZegbi, SaraGuerrero, InesSagüés, María FedericaOPTIMISED CULTURE MEDIAMESO-INOSITOLMANNITOLCHLAMYDOSPORESDUDDINGTONIA FLAGRANSBIOLOGICAL CONTROLGASTROINTESTINAL NEMATODEShttps://purl.org/becyt/ford/4.3https://purl.org/becyt/ford/4https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Duddingtonia flagrans is a microfungus used for the biological control of gastrointestinal nematodes in ruminants, which negatively impacts livestock production. This study aimed to evaluate chlamydospore production in different culture media and assess its impact on nematode predatory capacity. D. flagrans was cultured in enriched Glucose Sabouraud Agar (GSA-E) with the addition of meso-inositol (MI) and mannitol (M) at different concentrations: GSA-E+MI1.1%+M2%, GSA-E+MI1.1%+M5%, GSA-E+MI2%+M2%, GSA-E+MI2%M5% and GSA only (control). Twelve plates per concentration were incubated for 3, 4, and 5 weeks, respectively, at 27±0.5°C and 70±5% RH. Chlamydospores were quantified under optical microscope after mycelium homogenization. Nematophagous activity was assessed in faecal cultures with faeces from naturally parasitised sheep, incubated for 15 days at 24ºC. Infective larvae (L3) were recovered by baermannisation, quantified, and their reduction was calculated. Data were expressed as mean ±SEM. Normality was evaluated using the Shapiro-Wilk test. Group comparisons were performed using One-Way ANOVA and Dunnett’s tests or Kruskal-Wallis and Dunn’s tests. At 3, 4, and 5 weeks, respectively, the values were: GSA: 8.4×10⁶ (±1.1×10⁶), 8.2×10⁶ (±1.4×10⁶), 8.9×10⁶ (±1.2×10⁶); GSA-E+MI1.1%+M2%: 2.9×10⁷ (±4.8×106), 3.5×10⁷ (±3.4×106), 2.6×10⁷ (±4.3×106); GSA-E+MI1.1%+M5%: 3.2×10⁷ (±3.6×106), 8.7×10⁶ (±3.0×10⁶), 2.6×10⁷ (±6.6×106); GSA-E+MI2%+M2%: 8.9×10⁶ (±3.6×10⁶), 5.4×10⁶ (±1.6×10⁶), 1.7×10⁷ (±5.2×106); GSA-E+MI2%+M5%: 1.7×10⁷ (±5.9×106), 4.1×10⁷ (±8.6×106), 6.9×10⁷ (±1.3×10⁷). The GSA-E+MI2%+M5% medium optimised chlamydospore production at 5 weeks. The numbers of L3 recovered from MI- and M-enriched media were 74-99.7% (p<0.05) lower than in the control group. Supplementation with MI and M enhances chlamydospore production of D. flagrans without compromising its predatory capacity, thus optimising its production to use it in biological control against nematodes.Fil: Southwell, Manuela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Junco, Milagros. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Fernández, Alicia Silvina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Bernat, Gisele Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Zegbi, Sara. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Guerrero, Ines. Universidad Nacional del Centro de la Provincia de Buenos Aires. Facultad de Ciencias Veterinarias. Departamento de Sanidad Animal y Medicina Preventiva. Área Parasitología y Enfermedades Parasitarias; ArgentinaFil: Sagüés, María Federica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina30th Conference of the World Association for the Advancement of Veterinary ParasitologyCuritibaBrasilWorld Association for the Advancement of Veterinary ParasitologyWorld Association for the Advancement of Veterinary Parasitology2025info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectConferenciaBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/280025Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans; 30th Conference of the World Association for the Advancement of Veterinary Parasitology; Curitiba; Brasil; 2025; 199-200CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.waavp2025.comInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-06T12:03:10Zoai:ri.conicet.gov.ar:11336/280025instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-02-06 12:03:10.858CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| title |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| spellingShingle |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans Southwell, Manuela OPTIMISED CULTURE MEDIA MESO-INOSITOL MANNITOL CHLAMYDOSPORES DUDDINGTONIA FLAGRANS BIOLOGICAL CONTROL GASTROINTESTINAL NEMATODES |
| title_short |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| title_full |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| title_fullStr |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| title_full_unstemmed |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| title_sort |
Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans |
| dc.creator.none.fl_str_mv |
Southwell, Manuela Junco, Milagros Fernández, Alicia Silvina Bernat, Gisele Anahí Zegbi, Sara Guerrero, Ines Sagüés, María Federica |
| author |
Southwell, Manuela |
| author_facet |
Southwell, Manuela Junco, Milagros Fernández, Alicia Silvina Bernat, Gisele Anahí Zegbi, Sara Guerrero, Ines Sagüés, María Federica |
| author_role |
author |
| author2 |
Junco, Milagros Fernández, Alicia Silvina Bernat, Gisele Anahí Zegbi, Sara Guerrero, Ines Sagüés, María Federica |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
OPTIMISED CULTURE MEDIA MESO-INOSITOL MANNITOL CHLAMYDOSPORES DUDDINGTONIA FLAGRANS BIOLOGICAL CONTROL GASTROINTESTINAL NEMATODES |
| topic |
OPTIMISED CULTURE MEDIA MESO-INOSITOL MANNITOL CHLAMYDOSPORES DUDDINGTONIA FLAGRANS BIOLOGICAL CONTROL GASTROINTESTINAL NEMATODES |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/4.3 https://purl.org/becyt/ford/4 https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Duddingtonia flagrans is a microfungus used for the biological control of gastrointestinal nematodes in ruminants, which negatively impacts livestock production. This study aimed to evaluate chlamydospore production in different culture media and assess its impact on nematode predatory capacity. D. flagrans was cultured in enriched Glucose Sabouraud Agar (GSA-E) with the addition of meso-inositol (MI) and mannitol (M) at different concentrations: GSA-E+MI1.1%+M2%, GSA-E+MI1.1%+M5%, GSA-E+MI2%+M2%, GSA-E+MI2%M5% and GSA only (control). Twelve plates per concentration were incubated for 3, 4, and 5 weeks, respectively, at 27±0.5°C and 70±5% RH. Chlamydospores were quantified under optical microscope after mycelium homogenization. Nematophagous activity was assessed in faecal cultures with faeces from naturally parasitised sheep, incubated for 15 days at 24ºC. Infective larvae (L3) were recovered by baermannisation, quantified, and their reduction was calculated. Data were expressed as mean ±SEM. Normality was evaluated using the Shapiro-Wilk test. Group comparisons were performed using One-Way ANOVA and Dunnett’s tests or Kruskal-Wallis and Dunn’s tests. At 3, 4, and 5 weeks, respectively, the values were: GSA: 8.4×10⁶ (±1.1×10⁶), 8.2×10⁶ (±1.4×10⁶), 8.9×10⁶ (±1.2×10⁶); GSA-E+MI1.1%+M2%: 2.9×10⁷ (±4.8×106), 3.5×10⁷ (±3.4×106), 2.6×10⁷ (±4.3×106); GSA-E+MI1.1%+M5%: 3.2×10⁷ (±3.6×106), 8.7×10⁶ (±3.0×10⁶), 2.6×10⁷ (±6.6×106); GSA-E+MI2%+M2%: 8.9×10⁶ (±3.6×10⁶), 5.4×10⁶ (±1.6×10⁶), 1.7×10⁷ (±5.2×106); GSA-E+MI2%+M5%: 1.7×10⁷ (±5.9×106), 4.1×10⁷ (±8.6×106), 6.9×10⁷ (±1.3×10⁷). The GSA-E+MI2%+M5% medium optimised chlamydospore production at 5 weeks. The numbers of L3 recovered from MI- and M-enriched media were 74-99.7% (p<0.05) lower than in the control group. Supplementation with MI and M enhances chlamydospore production of D. flagrans without compromising its predatory capacity, thus optimising its production to use it in biological control against nematodes. Fil: Southwell, Manuela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Junco, Milagros. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Fernández, Alicia Silvina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Bernat, Gisele Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Zegbi, Sara. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina Fil: Guerrero, Ines. Universidad Nacional del Centro de la Provincia de Buenos Aires. Facultad de Ciencias Veterinarias. Departamento de Sanidad Animal y Medicina Preventiva. Área Parasitología y Enfermedades Parasitarias; Argentina Fil: Sagüés, María Federica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina 30th Conference of the World Association for the Advancement of Veterinary Parasitology Curitiba Brasil World Association for the Advancement of Veterinary Parasitology |
| description |
Duddingtonia flagrans is a microfungus used for the biological control of gastrointestinal nematodes in ruminants, which negatively impacts livestock production. This study aimed to evaluate chlamydospore production in different culture media and assess its impact on nematode predatory capacity. D. flagrans was cultured in enriched Glucose Sabouraud Agar (GSA-E) with the addition of meso-inositol (MI) and mannitol (M) at different concentrations: GSA-E+MI1.1%+M2%, GSA-E+MI1.1%+M5%, GSA-E+MI2%+M2%, GSA-E+MI2%M5% and GSA only (control). Twelve plates per concentration were incubated for 3, 4, and 5 weeks, respectively, at 27±0.5°C and 70±5% RH. Chlamydospores were quantified under optical microscope after mycelium homogenization. Nematophagous activity was assessed in faecal cultures with faeces from naturally parasitised sheep, incubated for 15 days at 24ºC. Infective larvae (L3) were recovered by baermannisation, quantified, and their reduction was calculated. Data were expressed as mean ±SEM. Normality was evaluated using the Shapiro-Wilk test. Group comparisons were performed using One-Way ANOVA and Dunnett’s tests or Kruskal-Wallis and Dunn’s tests. At 3, 4, and 5 weeks, respectively, the values were: GSA: 8.4×10⁶ (±1.1×10⁶), 8.2×10⁶ (±1.4×10⁶), 8.9×10⁶ (±1.2×10⁶); GSA-E+MI1.1%+M2%: 2.9×10⁷ (±4.8×106), 3.5×10⁷ (±3.4×106), 2.6×10⁷ (±4.3×106); GSA-E+MI1.1%+M5%: 3.2×10⁷ (±3.6×106), 8.7×10⁶ (±3.0×10⁶), 2.6×10⁷ (±6.6×106); GSA-E+MI2%+M2%: 8.9×10⁶ (±3.6×10⁶), 5.4×10⁶ (±1.6×10⁶), 1.7×10⁷ (±5.2×106); GSA-E+MI2%+M5%: 1.7×10⁷ (±5.9×106), 4.1×10⁷ (±8.6×106), 6.9×10⁷ (±1.3×10⁷). The GSA-E+MI2%+M5% medium optimised chlamydospore production at 5 weeks. The numbers of L3 recovered from MI- and M-enriched media were 74-99.7% (p<0.05) lower than in the control group. Supplementation with MI and M enhances chlamydospore production of D. flagrans without compromising its predatory capacity, thus optimising its production to use it in biological control against nematodes. |
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2025 |
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Enhacement of a solid culture medium for chlamydospore production of Duddingtonia flagrans; 30th Conference of the World Association for the Advancement of Veterinary Parasitology; Curitiba; Brasil; 2025; 199-200 CONICET Digital CONICET |
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