Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 May;11(3):e70341.
doi: 10.1002/vms3.70341.

Effect of Substituting Polyether Ionophore Anticoccidial Drugs With 1, 8-Cineole for the Control of Eimeria Infections in Broilers

Affiliations

Effect of Substituting Polyether Ionophore Anticoccidial Drugs With 1, 8-Cineole for the Control of Eimeria Infections in Broilers

Jing Sun et al. Vet Med Sci. 2025 May.

Abstract

Background: Coccidiosis is an important parasitic disease of broiler chickens. Drug resistance to the polyether polyether Ionophore anticoccidial drugs (PACDs) caused by long-term use has emerged as a significant problem in commercial broiler chicken production.

Objectives: This study explored the feasibility of 1,8-cineole (CIN) in replacing PACD with broiler feeding experiments and intestinal microecological experiments.

Methods: This experiment selected 21-day-old Lingnan yellow (LNY) broilers and randomly divided them into 8 groups, with 30 chickens in each group. They were uniformly fed with full feed during the breeding period. The experimental groups were as follows: (i) three broiler groups that were fed a PACD supplementation (G1: Salinomycin Premix [SAP] 60 mg/kg; G2: Monensin Premix [MOP] 100 mg/kg and G3: Maduramicin Premix [MAP] 5 mg/kg), (ii) three broiler groups that were administered different CIN dosages (G4: CIN-L 100 mg/kg, G5: CIN-M 150 mg/kg and G6: CIN-H 250 mg/kg) and (iii) two control broiler groups (G7: infected control group and G8: healthy control group). On the 23rd day, all groups were infected with coccidian cysts, except the G8 group which was used as a blank control. After 2 weeks of continuous feeding, the growth performance changes of broilers were analysed, and the intestinal lesions of eight groups of broilers were analysed after slaughter.

Results: Compared with PACD treatment, the average daily feed intake (ADFI) of the three CIN-treated groups increased by 13%, whereas the feed conversion ratio (FCR) reduced by 28%. FCR value for the high-dose CIN treatment was 2.04, 34% decline which compared with control group infected with spore oocysts. The anticoccidial index (ACI) of all PACD treatments was less than 120, whereas the ACI of the middle- and high-dose CIN treatments was higher than 180. In comparison to the Eimeria-infected control group, the diversity and total number of the microbiota in the CIN treatments increased significantly. Moreover, CIN treatment favoured the proliferation of intestinal probiotics, especially Lactobacillus sp.

Conclusions: CIN could have an inhibitory effect on parasite development as suggested in the gene function annotation of the intestinal microbiota. These results demonstrate that CIN may be a feasible natural alternative to anticoccidiosis drugs. So it was important to take precautions against and control coccidiosis in poultry production which has a lesser risk of creating resistance to substitutive PACDs.

Keywords: 1,8‐cineole; anticoccidial activity; broilers; intestinal microbial flora.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Blood stools in faeces of broilers infected with coccidian after 108 h (a) and cecum lesions of broilers infected with coccidian after 120 h (b). G1–G8 represent G1 group to G8 group, respectively. The yellow arrows point to the bloody stools, and red arrows point to the lesion.
FIGURE 2
FIGURE 2
The Shannon value, Chao value and PCoA of microbial flora in duodenum (a), small intestine (b) and cecum (c) of broilers.
FIGURE 3
FIGURE 3
Dominant genera in the intestines of broilers in the duodenum (a), small intestine (b) and cecum (c and d) of broilers.
FIGURE 4
FIGURE 4
The predicted KEGG function in microbial flora of duodenum (a), small intestine (b) and cecum (c).

Similar articles

References

    1. Aduayi, A. , Lamboni L., and Essodina T.. 2024. “Effects of Eucalyptus Globulus Leaves Powder on Growth Performance, Internal Organs Weights, Hematological and Biochemical Parameters of Isa Brown Pullets.” Journal of Applied Poultry Research 4: 100497–100497.
    1. Allen, P. C. , and Fetterer R. H.. 2002. “Recent Advances in Biology and Immunobiology of Eimeria Species and in Diagnosis and Control of Infection With these Coccidian Parasites of Poultry.” Clinical Microbiology Reviews 15: 58–65. 10.1128/cmr.15.1.58-65.2002. - DOI - PMC - PubMed
    1. Balacs, T. 1997. “Cineole‐Rich Eucalyptus.” International Journal of Aromatherapy 8: 15–21. doi 10.1016/S0962-4562(97)80020-3. - DOI
    1. Barwick, M. W. , Stevenson G. T., Johnston R. V., Casorso D. R., and Hymas T. A.. 1970. “Coccidiosis: Evaluation of Techniques for Battery Testing of Field‐Collected Eimeria Oocysts.” Experimental Parasitology 28: 37–41. doi 10.1016/0014-4894(70)90064-0. - DOI - PubMed
    1. Chapman, H. D. 1997. “Biochemical, Genetic and Applied Aspects of Drug Resistance in Eimeria Parasites of the Fowl.” Avian Pathology: Journal of the W.V.P.A 6: 221–244. 10.1080/03079459708419208. - DOI - PubMed

Publication types

MeSH terms

LinkOut - more resources