Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/9320 |
Resumo: | The aim of this study was to determine whether infection by Clostridium perfringens negatively interferes with the oxidant/antioxidant status and activity of energy metabolism enzymes (creatine kinase (CK), adenylate kinase (AK) and pyruvate kinase (PK)), as well as the zootechnical performance of broilers. A completely randomized design with three treatments, with five replications by treatment, and 10 birds by repetitions was used: T1: non-infected group; T2: group infected with C. perfringens; T3: group infected with C. perfringens, and basal diet with performance enhancers (antibiotic and coccidiostatic). At 21 days of age, the birds were experimentally infected orally with 4.0 x 108 CFU/mL C. perfringens. At strategic moments during the experimental period, zootechnical data and blood samples were collected. There were no significant differences among treatments in terms of weight gain, feed intake, or feed conversion. At 20 days, heterophils counts were significantly lower in the T3 group birds than in the others. A significant reduction in the number of total leukocytes, because of the lower number of lymphocytes, was observed in groups T2 and T3 on day 34. Neutrophil and monocyte counts were significantly lower in group T3 than in group T1 on day 34. On day 42, there were significantly lower levels of total protein and globulin in birds in T3 than in T1. On day 27, PK activity was significantly higher in groups T2 and T3; similar behavior observed on day 34 when CK and PK activities in T2 and T3 were significantly higher than those of T1. AK activity was significantly higher in the serum of T3 birds than in those of the other groups at 34 days. At 41 days, CK and PK activities were significantly higher only in birds in group T3 compared to other groups. The levels of reactive oxygen species and lipoperoxidation, as well as the activity of glutathione S-transferase, were significantly lower in birds from group T3 compared to other groups at age 20 days. After a challenge with C. perfringens, there were fluctuations in the behavior of oxidative stress biomarkers; in particular, at 41 days of age, birds in T2 had elevated levels of lipoperoxidation, different from what was seen in birds in T3 that consumed feed with a performance enhancer. Preliminary results suggest that clostridiosis affects serum activity of enzymes in the phosphotransfer network, requiring compensatory enzymatic changes in an attempt to maintain energy homeostasis. In addition, the infection reduces the number of inflammatory cells and causes oxidant/antioxidant imbalance that may contribute to the pathophysiology of the disease. Además, la infección reduce el número de células inflamatorias y provoca un desequilibrio en el estado oxidante / antioxidante que puede contribuir a la fisiopatología de la enfermedad. |
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Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilersRespuestas inflamatorias, enzimas del metabolismo energético, estado oxidativo en la infección por Clostridium perfringens en pollos de engordeRespostas inflamatórias, enzimas do metabolismo energético, status oxidativo na infecção por Clostridium perfringens em frangos de corteAntioxidanteATPClostridiosisPatogénesisPollos.AntioxidanteATPAvesClostridiosePatogênese.AntioxidantATPBirdsClostridiosisPathogenesis.The aim of this study was to determine whether infection by Clostridium perfringens negatively interferes with the oxidant/antioxidant status and activity of energy metabolism enzymes (creatine kinase (CK), adenylate kinase (AK) and pyruvate kinase (PK)), as well as the zootechnical performance of broilers. A completely randomized design with three treatments, with five replications by treatment, and 10 birds by repetitions was used: T1: non-infected group; T2: group infected with C. perfringens; T3: group infected with C. perfringens, and basal diet with performance enhancers (antibiotic and coccidiostatic). At 21 days of age, the birds were experimentally infected orally with 4.0 x 108 CFU/mL C. perfringens. At strategic moments during the experimental period, zootechnical data and blood samples were collected. There were no significant differences among treatments in terms of weight gain, feed intake, or feed conversion. At 20 days, heterophils counts were significantly lower in the T3 group birds than in the others. A significant reduction in the number of total leukocytes, because of the lower number of lymphocytes, was observed in groups T2 and T3 on day 34. Neutrophil and monocyte counts were significantly lower in group T3 than in group T1 on day 34. On day 42, there were significantly lower levels of total protein and globulin in birds in T3 than in T1. On day 27, PK activity was significantly higher in groups T2 and T3; similar behavior observed on day 34 when CK and PK activities in T2 and T3 were significantly higher than those of T1. AK activity was significantly higher in the serum of T3 birds than in those of the other groups at 34 days. At 41 days, CK and PK activities were significantly higher only in birds in group T3 compared to other groups. The levels of reactive oxygen species and lipoperoxidation, as well as the activity of glutathione S-transferase, were significantly lower in birds from group T3 compared to other groups at age 20 days. After a challenge with C. perfringens, there were fluctuations in the behavior of oxidative stress biomarkers; in particular, at 41 days of age, birds in T2 had elevated levels of lipoperoxidation, different from what was seen in birds in T3 that consumed feed with a performance enhancer. Preliminary results suggest that clostridiosis affects serum activity of enzymes in the phosphotransfer network, requiring compensatory enzymatic changes in an attempt to maintain energy homeostasis. In addition, the infection reduces the number of inflammatory cells and causes oxidant/antioxidant imbalance that may contribute to the pathophysiology of the disease. Además, la infección reduce el número de células inflamatorias y provoca un desequilibrio en el estado oxidante / antioxidante que puede contribuir a la fisiopatología de la enfermedad.El objetivo de este estudio fue determinar si la infección por Clostridium perfringens interfiere negativamente con el estado oxidante / antioxidante y la actividad de las enzimas del metabolismo energético (creatina quinasa (CK), adenilato quinasa (AK) y piruvato quinasa (PK)), así como comportamiento zootécnico de pollos de engorde. O delineamento experimental foi inteiramente casualizado com três tratamentos, com cinco repetições por tratamento e 10 pollos por repetições: T1: grupo no infectado; T2: grupo infectado por C. perfringens; T3: grupo infectado por C. perfringens y dieta basal con promotores del crecimiento (antibiótico y coccidiostático). A los 21 días de edad, las aves fueron infectadas experimentalmente por vía oral con 4.0 x 108 UFC/mL de C. perfringens. En momentos estratégicos del período experimental, fueron recolectaron datos zootécnicos y muestras de sangre. No hubo diferencias significativas entre los tratamientos en términos de aumento de peso, consumo de alimento y conversión alimenticia. A los 20 días, los recuentos de heterófilos fueron significativamente más bajos en las pollos del grupo T3 que en las otras pollos. Se observó una reducción significativa en el número de leucocitos totales, debido al menor número de linfocitos, en los grupos T2 y T3 el día 34. Los recuentos de neutrófilos y monocitos fueron significativamente más bajos en el grupo T3 que en el grupo T1 el día 34. El día 42, hubo niveles significativamente más bajos de proteína total y globulina en pollos de T3 en comparación con T1. El día 27, la actividad PK fue significativamente mayor en los grupos T2 y T3; comportamiento similar observado en el día 34 cuando las actividades de CK y PK en T2 y T3 fueron significativamente mayores en relación con T1. La actividad de AK fue significativamente mayor en el suero de pollos de engorde T3 en comparación con los otros grupos a los 34 días. A los 41 días, las actividades de CK y PK fueron significativamente más altas sólo en las aves del grupo T3 en comparación con los otros grupos. Los niveles de especies reactivas al oxígeno y la lipoperoxidación, así como la actividad de la glutatión S-transferasa, fueron significativamente menores en los pollos del grupo T3 en comparación con otros grupos a los 20 días de edad. Después de un desafío con C. perfringens, hubo fluctuaciones en el comportamiento de los biomarcadores de estrés oxidativo; en particular, a los 41 días de edad, los pollos de T2 mostraron altos niveles de lipoperoxidación, diferente a lo observado en pollos de T3 que consumieron alimento con promotores de crecimiento. Estos resultados preliminares sugieren que la clostridiosis afecta la actividad sérica de las enzimas en la red de fosfotransferencia, lo que requiere cambios enzimáticos compensatorios en un intento por mantener la homeostasis energética.O objetivo deste estudo foi determinar se a infecção por Clostridium perfringens interfere negativamente no status oxidante / antioxidante e na atividade das enzimas do metabolismo energético (creatina quinase (CK), adenilato quinase (AK) e piruvato quinase (PK)), bem como no desempenho zootécnico de frangos de corte. O delineamento experimental foi inteiramente casualizado com três tratamentos, com cinco repetições por tratamento e 10 aves por repetições: T1: grupo não infectado; T2: grupo infectado com C. perfringens; T3: grupo infectado com C. perfringens e dieta basal com promotores de crescimento (antibiótico e coccidiostático). Aos 21 dias de idade, as aves foram infectadas experimentalmente por via oral com 4,0 x 108 UFC/mL de C. perfringens. Em momentos estratégicos do período experimental, foram coletados dados zootécnicos e amostras de sangue. Não houve diferenças significativas entre os tratamentos em termos de ganho de peso, consumo de ração e conversão alimentar. Aos 20 dias, as contagens de heterófilos foram significativamente menores nas aves do grupo T3 do que nas outras. Foi observada uma redução significativa no número de leucócitos totais, devido ao menor número de linfócitos nos grupos T2 e T3 no dia 34. As contagens de neutrófilos e monócitos foram significativamente menores no grupo T3 do que no grupo T1 no dia 34. No dia 42, houve níveis significativamente menores de proteína total e globulina nas aves do T3 em relação ao T1. No dia 27, a atividade da PK foi significativamente maior nos grupos T2 e T3; comportamento semelhante observado no dia 34 quando as atividades de CK e PK em T2 e T3 foram significativamente maiores em relação ao T1. A atividade de AK foi significativamente maior no soro das aves do T3 em comparação aos outros grupos aos 34 dias. Aos 41 dias, as atividades de CK e PK foram significativamente maiores apenas nas aves do grupo T3 em comparação com os outros grupos. Os níveis de espécies reativas ao oxigênio e lipoperoxidação, bem como a atividade da glutationa S-transferase, foram significativamente menores nas aves do grupo T3 em relação com os outros grupos aos 20 dias de idade. Após um desafio com C. perfringens, houve flutuações no comportamento dos biomarcadores de estresse oxidativo; em particular, aos 41 dias de idade, as aves do T2 apresentaram níveis elevados de lipoperoxidação, diferente do que foi observado em aves do T3 que consumiram ração com promotores de crescimento. Estes resultados preliminares sugerem que a clostridiose afeta a atividade sérica de enzimas da rede de fosfotransferência, o que exige alterações enzimáticas compensatórias na tentativa de manter a homeostase energética. Além disso, a infecção reduz o número de células inflamatórias e causa desequilíbrio no status oxidante/antioxidante que pode contribuir para a fisiopatologia da doença.Research, Society and Development2020-11-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/932010.33448/rsd-v9i11.9320Research, Society and Development; Vol. 9 No. 11; e4969119320Research, Society and Development; Vol. 9 Núm. 11; e4969119320Research, Society and Development; v. 9 n. 11; e49691193202525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/9320/9030Copyright (c) 2020 Gabriela Miotto Galli; Marcel Manente Boiago; Carine Freitas de Souza; Lorenzo Binotto Abbad; Matheus Dellamea Baldissera; Aleksandro Schafer Da Silvahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessGalli, Gabriela Miotto Boiago, Marcel Manente Souza, Carine Freitas de Abbad, Lorenzo Binotto Baldissera, Matheus Dellamea Silva, Aleksandro Schafer Da 2020-12-10T23:37:57Zoai:ojs.pkp.sfu.ca:article/9320Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:31:38.107130Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers Respuestas inflamatorias, enzimas del metabolismo energético, estado oxidativo en la infección por Clostridium perfringens en pollos de engorde Respostas inflamatórias, enzimas do metabolismo energético, status oxidativo na infecção por Clostridium perfringens em frangos de corte |
title |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
spellingShingle |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers Galli, Gabriela Miotto Antioxidante ATP Clostridiosis Patogénesis Pollos. Antioxidante ATP Aves Clostridiose Patogênese. Antioxidant ATP Birds Clostridiosis Pathogenesis. |
title_short |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
title_full |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
title_fullStr |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
title_full_unstemmed |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
title_sort |
Inflammatory responses, energy metabolism enzymes, oxidative status in Clostridium perfringens infection in broilers |
author |
Galli, Gabriela Miotto |
author_facet |
Galli, Gabriela Miotto Boiago, Marcel Manente Souza, Carine Freitas de Abbad, Lorenzo Binotto Baldissera, Matheus Dellamea Silva, Aleksandro Schafer Da |
author_role |
author |
author2 |
Boiago, Marcel Manente Souza, Carine Freitas de Abbad, Lorenzo Binotto Baldissera, Matheus Dellamea Silva, Aleksandro Schafer Da |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Galli, Gabriela Miotto Boiago, Marcel Manente Souza, Carine Freitas de Abbad, Lorenzo Binotto Baldissera, Matheus Dellamea Silva, Aleksandro Schafer Da |
dc.subject.por.fl_str_mv |
Antioxidante ATP Clostridiosis Patogénesis Pollos. Antioxidante ATP Aves Clostridiose Patogênese. Antioxidant ATP Birds Clostridiosis Pathogenesis. |
topic |
Antioxidante ATP Clostridiosis Patogénesis Pollos. Antioxidante ATP Aves Clostridiose Patogênese. Antioxidant ATP Birds Clostridiosis Pathogenesis. |
description |
The aim of this study was to determine whether infection by Clostridium perfringens negatively interferes with the oxidant/antioxidant status and activity of energy metabolism enzymes (creatine kinase (CK), adenylate kinase (AK) and pyruvate kinase (PK)), as well as the zootechnical performance of broilers. A completely randomized design with three treatments, with five replications by treatment, and 10 birds by repetitions was used: T1: non-infected group; T2: group infected with C. perfringens; T3: group infected with C. perfringens, and basal diet with performance enhancers (antibiotic and coccidiostatic). At 21 days of age, the birds were experimentally infected orally with 4.0 x 108 CFU/mL C. perfringens. At strategic moments during the experimental period, zootechnical data and blood samples were collected. There were no significant differences among treatments in terms of weight gain, feed intake, or feed conversion. At 20 days, heterophils counts were significantly lower in the T3 group birds than in the others. A significant reduction in the number of total leukocytes, because of the lower number of lymphocytes, was observed in groups T2 and T3 on day 34. Neutrophil and monocyte counts were significantly lower in group T3 than in group T1 on day 34. On day 42, there were significantly lower levels of total protein and globulin in birds in T3 than in T1. On day 27, PK activity was significantly higher in groups T2 and T3; similar behavior observed on day 34 when CK and PK activities in T2 and T3 were significantly higher than those of T1. AK activity was significantly higher in the serum of T3 birds than in those of the other groups at 34 days. At 41 days, CK and PK activities were significantly higher only in birds in group T3 compared to other groups. The levels of reactive oxygen species and lipoperoxidation, as well as the activity of glutathione S-transferase, were significantly lower in birds from group T3 compared to other groups at age 20 days. After a challenge with C. perfringens, there were fluctuations in the behavior of oxidative stress biomarkers; in particular, at 41 days of age, birds in T2 had elevated levels of lipoperoxidation, different from what was seen in birds in T3 that consumed feed with a performance enhancer. Preliminary results suggest that clostridiosis affects serum activity of enzymes in the phosphotransfer network, requiring compensatory enzymatic changes in an attempt to maintain energy homeostasis. In addition, the infection reduces the number of inflammatory cells and causes oxidant/antioxidant imbalance that may contribute to the pathophysiology of the disease. Además, la infección reduce el número de células inflamatorias y provoca un desequilibrio en el estado oxidante / antioxidante que puede contribuir a la fisiopatología de la enfermedad. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-11-22 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/9320 10.33448/rsd-v9i11.9320 |
url |
https://rsdjournal.org/index.php/rsd/article/view/9320 |
identifier_str_mv |
10.33448/rsd-v9i11.9320 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/9320/9030 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 9 No. 11; e4969119320 Research, Society and Development; Vol. 9 Núm. 11; e4969119320 Research, Society and Development; v. 9 n. 11; e4969119320 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052803919642624 |