4.7 Article

Anticoccidial Activity of Qinghao Powder Against Eimeria tenella in Broiler Chickens

Journal

FRONTIERS IN VETERINARY SCIENCE
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fvets.2021.709046

Keywords

Eimeria tenella; Qinghao Powder (QHP); recommended dose (RD); safety test; target animal

Funding

  1. Agricultural Science and Technology Innovation Program of Chinese Academy of Agricultural Sciences [CAAS-ASTIP-2014-LIHPS-04]
  2. Major Output Scientific Research Items of Chinese Academy of Agricultural Sciences [CAAS-ZDXT2018008-4]
  3. Special Fund of the Chinese Central Government for Basic Scientific Research Operations in Commonweal Research Institutes [1610322020005]
  4. Natural Science Foundation of Gansu Province [18JR3RA398]

Ask authors/readers for more resources

The study indicates that a dose of 0.30 g/kg Qinghao Powder in feed is appropriate for therapy and intermittent treatment of E. tenella-infected chicks. The dosage in clinical applications should be set according to the recommended dose to ensure animal safety.
Artemisia annua (AAH) is traditionally used as an anti-malarial, expectorant and antipyretic Chinese medicine. The aim of this study was to explore the therapeutic effect of Qinghao Powder (QHP) on chicken coccidiosis, evaluate the safe dosage of QHP, and provide test basis for clinical medication. High-performance liquid chromatography (HPLC) and thin-layer chromatography (TLC) were used to detect artemisinin in Qinghao Powder (QHP) for quality control. The level of artemisinin in QHP was 81.03 mg/g. A total of 210 chicks (14 days of age) were divided randomly into seven groups: three QHP treatments (0.15, 0.30, and 0.60 g/kg), a toltrazuril control (1.00 mL/L), a sulfachloropyrazine sodium control (SSC, 0.30 g/L), an E. tenella-infected control, and a healthy control group. All the groups were inoculated orally with 7 x 10(4) E. tenella oocysts except for the healthy control group. After seven days of administration, compared with the infected control group, chicks which were administered QHP, SS, and toltrazuril showed less bloody feces, oocyst output, and cecal lesions, and the protection rates were improved. The maximum rBWG and ACI were found in the SS-medicated group, followed by the groups medicated with 0.60 and 0.30 g/kg QHP. Therefore, a 0.30 g/kg dose level of QHP in the feed was selected as the recommend dose (RD) in the target animal safety test, in which 80 broiler chicks (14 days of age) were randomly divided into four major groups (I-healthy control group; II-1x RD; III-3x RD; IV-6x RD), with each group subdivided into two subgroups (A and B) consisting of 10 chicks each. After 7-day (for sub-group A) or 14-day (for sub-group B) administration, compared with the healthy control, treatment-related changes in BWG, feed conversion ratio (FCR), relative organ weight (ROW) of the liver, WBC counts, and levels of RBC, HGB, ALT, AST, and TBIL were detected in the 3x and 6x RD groups. No differences were noted in necropsy for all doses, and histopathological examinations exhibited no QHP-associated signs of toxicity or abnormalities in the liver or kidney. The findings suggest that QHP at a dose of 0.30 g/kg feed would be appropriate for therapy and intermittent treatment of E. tenella-infected chicks, the dosage in clinical applications should be set according to the recommended dose to ensure animal safety.

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