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1.
Parasit Vectors ; 13(1): 56, 2020 Feb 11.
Article in English | MEDLINE | ID: mdl-32046772

ABSTRACT

BACKGROUND: Eimeria spp. are responsible for chicken coccidiosis which is the most important enteric protozoan disease resulting in tremendous economic losses in the poultry industry. Understanding the interaction between the avian cecal microbiota and coccidia is of interest in the development of alternative treatments that do not rely on chemotherapeutics and do not lead to drug resistance. METHODS: We utilized 16S rRNA gene sequencing to detect the dynamics of the cecal microbial community in AA broilers challenged with Eimeria tenella. Histopathological analysis of the cecum was also conducted. RESULTS: We found that microbial shifts occur during the infection. Lactobacillus, Faecalibacterium, Ruminococcaceae UCG-013, Romboutsia and Shuttleworthia decreased in abundance. However, the opportunistic pathogens Enterococcus and Streptococcus increased in abundance over time in response to the infection. CONCLUSIONS: Eimeria tenella disrupts the integrity of the cecal microbiota and could promote the establishment and growth of potentially pathogenic bacteria. Defining bacterial populations affected by coccidial infection might help identify bacterial markers for intestinal disease as well as populations or species that could be beneficial in maintaining and restoring gut homeostasis during and after infection with E. tenella.


Subject(s)
Chickens , Coccidiosis/veterinary , Eimeria tenella , Gastrointestinal Microbiome/genetics , Poultry Diseases/parasitology , Animals , Bacteria/classification , Bacteria/isolation & purification , Cecum/microbiology , Cecum/parasitology , Cecum/pathology , Chickens/microbiology , Chickens/parasitology , Coccidiosis/therapy , Eimeria tenella/genetics , Eimeria tenella/parasitology , Metagenomics , RNA, Ribosomal, 16S/genetics
2.
Ciênc. rural ; 39(5): 1471-1477, ago. 2009. graf, tab
Article in English | LILACS | ID: lil-521195

ABSTRACT

In the first trial a total of 250 day-old male chicks were distributed into five treatments and given the following diets: a diet with growth promoter; a diet without added growth promoter; a diet added with avilamycin only; diet supplemented with 0.5g of oregano oil kg diet-1; 1.0g of oregano oil kg diet-1. In other trial a total of 288 day-old chicks was used and distributed into four treatments, which were given the following diets: a diet with anticoccidial agent; a diet without anticoccidial agent; a diet supplemented with 0.5g of oregano oil kg diet-1; a 1.0g of oregano oil kg diet-1. In the first trial the nonmedicated group had the highest crypt depth which differs from chickens fed with growth promoter or with 0.5 and 1.0g of oregano oil kg diet-1. The broilers fed with positive control (antibiotic and anticoccidial) had the highest villous: crypt ratio compared with the negative control that had the lowest villous:crypt ratio and the highest oocyst excretion in litter (P<0.05) In the second trial it was observed that broilers fed with non anticoccidial agent had the highest cecal lamina propria thickeness which differ from chickens fed with anticoccidial agent in diet or supplemented with 1.0 of oregano oil kg diet-1 (P<0.05).


Inicialmente, foram utilizados, neste estudo, 250 pintos de um dia de idade distribuídos em cinco tratamentos: dieta com promotor de crescimento; dieta sem promotor de crescimento; dieta contendo somente antibiótico; dieta com 0,5g de orégano óleo kg de ração-1 ou com 1,0g de orégano óleo kg de ração-1. No outro ensaio, foram utilizados 288 pintos de um dia de idade distribuídos em quatro grupos: dieta com anticoccidiano; dieta sem anticoccidiano; dieta com 0,5g de orégano óleo kg dieta-1 ou 1,0g de orégano óleo kg de ração-1. No primeiro ensaio, o grupo tratado sem promotor de crescimento apresentou a maior profundidade de cripta quando comparada com os animais tratados com promotor de crescimento ou com 0,5 e 1,0g de orégano óleo kg de ração-1. Os frangos que receberam a dieta com promotor de crescimento (antibiótico+anticoccidiano) apresentaram uma maior relação vilo:cripta em comparação com os frangos do controle negativo, os quais tiveram a menor relação vilo:cripta e uma maior excreção de oocistos por grama de fezes (P<0.05). No segundo ensaio, observou-se que os frangos alimentados com dieta sem anticoccidiano tiveram uma maior espessura de lâmina própria cecal, diferindo dos frangos tratados com anticoccidiano ou com 1,0 de orégano óleo kg de ração-1 (P <0,05).


Subject(s)
Animals , Coccidiosis/veterinary , Diet/methods , Diet/veterinary , Eimeria tenella/isolation & purification , Eimeria tenella/parasitology , Phytotherapy/veterinary , Intestinal Mucosa/parasitology , Origanum , Poultry
3.
Exp Parasitol ; 81(1): 29-38, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7628564

ABSTRACT

In this study, the intraepithelial leukocytes supposedly involved in the transportation of Eimeria tenella sporozoites through the cecal lamina propria were phenotypically characterized. The ceca of naive and immune chickens were examined at various times after inoculation by light microscopy and immunocytochemical techniques. The distribution of sporozoites within the villus differed markedly between both groups. From 16 hr postinoculation, significantly fewer sporozoites had reached the crypts in immune chickens, and schizont formation was inhibited. In the villus epithelium of both naive and immune chickens, few sporozoites were found within a leukocyte. Using anti-sporozoite and anti-CD45 monoclonals, we showed that even when intraepithelial leukocytes are abundantly present, only a few sporozoites were inside them. In the lamina propria of immune chickens significantly more sporozoites were found within leukocytes than in the lamina propria of naive chickens. The phenotype of the few leukocytes that harbored sporozoites was similar in naive and immune chickens. A few sporozoites were detected in B cells, 10% in macrophages, and 50% in T cells, especially CD8+ cells. These results show that E. tenella sporozoites rarely enter intraepithelial leukocytes and therefore their putative role in transporting sporozoites through the lamina propria is doubtful.


Subject(s)
Cecum/parasitology , Coccidiosis/physiopathology , Eimeria tenella/physiology , Eimeria tenella/parasitology , Intestinal Mucosa/parasitology , Leukocytes/parasitology , Animals , Chickens , Coccidiosis/immunology , Eimeria tenella/immunology , Epithelium/parasitology , Time Factors
4.
Vet. Méx ; 25(3): 215-9, jul.-sept. 1994. tab
Article in Spanish | LILACS | ID: lil-187976

ABSTRACT

Se realizó un estudio con pollos de engorda alojados en piso, con el objeto de comparar la eficacia de una vacuna con Eimeria tenella, E. necatrix, E. acervulina y E. máxima contra el ionóforo narazina en el alimento en la prevención de coccidiosis. Se emplearon 320 pollos, divididos en cuatro lotes, cada uno con 4 repeticiones de 20 aves. El lote a recibió alimento sin coccidiostato. A las tres semanas de iniciado el experimento, los tres fueron confrontados con un inóculo formado con una mezcla de E. tenella, E. necatrix, E. acervulina y E. máxima. El lote D fue testigo negativo. Las variables registradas fueron peso, consumo de alimentos, índice de ooquistes en heces y cama, lesiones, mortalidad y pigmentación de los tarsos. Los resultados mostraron diferencias significativas entre las 0-4 semanas en la ganancia de peso y conversión alimenticia, la mejor ganancia de peso correspondió al grupo D, seguida del A, B y C, respectivamente. La conversión alimenticia fue más eficiente para el grupo D. Los datos de 4 a 7 y de 0 a 7 semanas no mostraron diferencias estadísticas en ninguno de los parámetros analizados. El índice anticoccidial fue el mejor para el grupo A seguido del B y C, respectivamente, lo cual indica que el inmunógeno proporcionó una adecuada protección contra la coccidiosis aviar


Subject(s)
Chickens/physiology , Chickens/immunology , Chickens/microbiology , Eimeria tenella/immunology , Eimeria tenella/parasitology , Eimeria tenella/pathogenicity , Ionophores/administration & dosage , Ionophores/pharmacokinetics , Ionophores/immunology , Vaccination/methods , Vaccination , Vaccination/veterinary
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