Analysis of Chicken Gut Microbiome Fed by Phyllanthus urinaria as Phytobiotic Using 16S rRNA Metagenome
محورهای موضوعی : CamelH. Khasanah 1 , W.I.D. Fanata 2 , D.E. Kusbianto 3
1 - Un
2 - Department of Agrotechnology, Faculty of Agriculture, University of Jember, Indonesia
3 - Department of Agricultural Science, Faculty of Agriculture, University of Jember, Indonesia
کلید واژه: Broiler, meniran leaf, metagenomic, microbiota,
چکیده مقاله :
Applying of antibiotic growth promoters (AGPs) in chicken has been forbidden due to leaving residues and resistance in people who consume them, especially in livestock products. The provision of phytobiotics as AGPs substitute for chickens increases their immunity and productivity. Phytobiotics may threaten pathogenic bacteria or promote colonization of beneficial bacteria for chickens. This study analyzed the effect of meniran leaves (Phyllanthus urinaria) as a phytobiotic and an alternative for AGPs on the abundance, diversity, and composition of the chicken gut microbial community. The microbial ecology of chicken gut used the molecular markers of the 16S rRNA amplicon sequencing V3-V4 region. Samples were 20 chickens maintained for 21 days and fed according to basal requirements that were divided into two treatments, namely 0% phytobiotic provision (T0) and 2% meniran leaves phytobiotic provision. The sequencing libraries were constructed by utilizing the Ion Plus Fragment Library Kit 48 rxns. The sequencing result was evaluated by performing single-ends reads quality control, operational taxonomic units (OTUs) clustering, species annotation, and diversity within groups (alpha diversity). The outcome data revealed that Firmicutes was the predominant phylum in both samples. Based on the class level, T0 was identified to have 100% Bacteroidia, while T1 was detected to have 78% Bacteroidia and 22% Flavobacteriia. Based on the order level, T0 was dominated by the Negativicutes and T1 was dominated by the Selenomonadales. Based on the genus level, T0 was dominated by the Megamonas and T1 was dominated by the Lactobacillus. The OTUs of T0 and T1 were 126 and 144. This study concludes that the Phyllanthus urinaria provision as a phytobiotic influences the diversity, relative abundance, and composition of the chicken gut microbiota.
Ali M., Khan T., Fatima K., Ali Q., Ul A., Ovais M., Khalil A.T., Ullah I., Raza A., Shinwari Z.K. and Idrees M. (2018). Selected hepatoprotective herbal medicines: Evidence from ethnomedicinal applications, animal models, and possible mechanism of actions. Phytother. Res. 32, 199-215.
Allaire J.M., Crowley S.M., Law H.T., Chang S.Y., Ko H.J. and Vallance B.A. (2018). The intestinal epithelium: Central coordinator of mucosal immunity. Trends in Immunol. 39, 677-696.
Asrore M., Shaufi M., Sieo C.C., Chong C.W., Gan H.M. and Ho Y.W. (2015). Deciphering chicken gut microbial dynamics based on high-throughput 16S rRNA metagenomics analyses. Gut Pathog. 7, 1-12.
Astuti P. and Suripta H. (2020). Performance of broiler chicken carcass provided with water extract (Phyllanthus niruri) and Moringa (Moringa oleifera). Bantara J. Anim. Sci. 2, 2657-1587.
Bhogoju S., Nahashon S., Wang X., Darris C. and Kilonzo-Nthenge A. (2018). A comparative analysis of microbial profile of Guinea fowl and chicken using metagenomic approach. PLoS One. 13, e0191029.
Bokulich N.A., Subramanian S., Faith J.J., Gevers D., Gordon J.I., Knight R., Mills D.A. and Caporaso J.G. (2013). Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing. Nat. Methods. 10, 57-59.
Brower C.H., Mandal S., Hayer S., Sran M., Zehra A., Patel S.J., Kaur R., Chatterjee L., Mishra S., Das B.R., Singh P., Singh R., Gill J.P.S. and Laxminarayan R. (2017). The prevalence of extended-spectrum beta-lactamase-producing multidrug-resistant Escherichia coli in poultry chickens and variation according to farming practices in Punjab, India. Environ. Health Perspect. 125, 77015-77010.
Caporaso J.G., Kuczynski J., Stombaugh J., Bittinger K., Bushman F.D., Costello E.K., Fierer N., Pẽa A.G., Goodrich J. K., Gordon J.I., Huttley G.A., Kelley S.T., Knights D., Koenig J.E., Ley R.E., Lozupone C.A., McDonald D., Muegge B.D., Pirrung M. and Knight R. (2010). QIIME allows analysis of high-throughput community sequencing data. Nat. Methods. 7, 335-336.
Castanon J.I.R. (2007). History of the use of antibiotic as growth promoters in European poultry feeds. Poult. Sci. 86, 2466-2471.
Chandra Das N., Abony M., Banik A., Akhter Akhi M., Hossain A.K.M.N. and Ahmed Z. (2020). Optimization of bacteriocin producing probiotic Lactobacillus spp. isolated from broiler chicken gut. SSRN Electron. J. 2, 1-8.
Danzeisen J.L., Kim H.B., Isaacson R.E., Tu Z.J. and Johnson T.J. (2011). Modulations of the chicken cecal microbiome and metagenome in response to anticoccidial and growth promoter treatment. PLoS One. 6, e27949.
Edgar R.C. (2004). MUSCLE: Multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32, 1792-1797.
Edgar R.C., Haas B.J., Clemente J.C., Quince C. and Knight R. (2011). UCHIME improves sensitivity and speed of chimera detection. Bioinformatics. 27, 2194-2200.
Eldeen I.M.S., Seow E.M., Abdullah R. and Sulaiman S.F. (2011). In vitro antibacterial, antioxidant, total phenolic contents and anti-HIV-1 reverse transcriptase activities of extracts of seven Phyllanthus sp. South African J. Botany. 77, 75-79.
Feng W., Ao H., Peng C. and Yan D. (2019). Gut microbiota, a new frontier to understand traditional Chinese medicines. Pharmacol. Res. 142, 176-191.
Geethangili M. and Ding S.T. (2018). A review of the phytochemistry and pharmacology of Phyllanthus urinaria. Front. Pharmacol. 9, 1109-1115.
Harvey A.L., Edrada-Ebel R. and Quinn R.J. (2015). The re-emergence of natural products for drug discovery in the genomics era. Nat. Rev. Drug Discov. 14, 111-129.
Hess M., Sczyrba A., Egan R., Kim T.W., Chokhawala H., Schroth G., Luo S., Clark D.S., Chen F., Zhang T., Mackie R.I., Pennacchio L.A., Tringe S.G., Visel A., Woyke T., Wang Z. and Rubin E.M. (2011). Metagenomic discovery of biomass-degrading genes and genomes from cow rumen. Science. 331, 463-467.
Hidanah S., Sabdoningrum E.K., Wahjuni R.S. and Chusniati S. (2018). Effects of meniran (Phyllanthus niruri) administration on leukocyte profile of broiler chickens infected with Mycoplasma gallisepticum. Vet. World. 11, 834-839.
Huang P., Zhang Y., Xiao K., Jiang F., Wang H., Tang D., Liu D., Liu B., Liu Y., He X., Liu H., Liu X., Qing Z., Liu C., Huang J., Ren Y., Yun L., Yin L., Lin Q. and Zeng J. (2018). The chicken gut metagenome and the modulatory effects of plant-derived benzylisoquinoline alkaloids 06 biological sciences 0605 microbiology. Microbiome. 6, 211-217.
Huang S.T., Huang C.C., Sheen J.M., Lin T.K., Liao P.L., Huang W.L., Wang P.W., Liou C.W. and Chuang J.H. (2016). Phyllanthus urinaria ’s inhibition of human osteosarcoma xenografts growth in mice is associated with modulation of mitochondrial fission/fusion machinery. American J. Chinese Med. 44, 1507-1523.
Hubert S.M., Al-Ajeeli M., Bailey C.A. and Athrey G. (2019). The role of housing environment and dietary protein source on the gut microbiota of chicken. Animals. 9, 1085-1095.
Hugerth L.W. and Andersson A.F. (2017). Analysing microbial community composition through amplicon sequencing: From sampling to hypothesis testing. Front. Microbiol. 8, 1561-1569.
Lekshmi M., Ammini P., Kumar S. and Varela M.F. (2017). The food production environment and the development of antimicrobial resistance in human pathogens of animal origin. Microorganisms. 5, 11-17.
Li B., Zhang X., Guo F., Wu W. and Zhang T. (2013). Characterization of tetracycline resistant bacterial community in saline activated sludge using batch stress incubation with high-throughput sequencing analysis. Water Res. 47, 4207-4216.
Lundberg D.S., Yourstone S., Mieczkowski P., Jones C.D. and Dangl J.L. (2013). Practical innovations for high-throughput amplicon sequencing. Nat. Methods. 10, 999-1002.
Muaz K., Riaz M., Akhtar S., Park S. and Ismail A. (2018). Antibiotic residues in chicken meat: Global prevalence, threats, and decontamination strategies: A review. J. Food Protec. 81, 619-627.
Nandhakumar E. and Indumathi P. (2013). In vitro antioxidant activities of methanol and aqueous extract of Annona squamosa fruit pulp. J. Acupunct. Meridian Stud. 6, 142-148.
Nguyen T.H.K. and Nguyen M.D. (2013). Antimicrobial activities of Phyllanthus urinaria extracts before and after combined with Pandanus tectorious and Lactobacillus rhamnosus PN04. Biomed. Pharmacol. J. 6, 241-247.
NRC. (1994). Nutrient Requirements of Poultry, 9th Rev. Ed. National Academy Press, Washington, DC., USA.
Ogbuewu I.P., Okoro V.M. and Mbajiorgu C.A. (2020). Meta-analysis of the influence of phytobiotic (pepper) supplementation in broiler chicken performance. Trop. Anim. Health Prod. 52, 17-30.
Rychlik I. (2020). Composition and function of chicken gut microbiota. Animals. 10, 103-110.
Salaheen S., Kim S.W., Haley B.J., Van Kessel J.A.S. and Biswas D. (2017). Alternative growth promoters modulate broiler gut microbiome and enhance body weight gain. Front. Microbiol. 8, 2088-2095.
Sinurat A.P., Wina E., Rakhmani S.I.W., Wardhani T., Haryati T., and Purwadaria T. (2018). Bioactive substances of some herbals and their effectiveness as antioxidant, antibacteria and antifungi. Indonesian J. Anim. Vet. Sci. 23, 18-28.
Stanley D., Hughes R.J. and Moore R.J. (2014). Microbiota of the chicken gastrointestinal tract: Influence on health, productivity and disease. Appl. Microbiol. Biotechnol. 98, 4301-4310.
Umiarti A.P. (2020). Manajemen Pemeliharaan Ayam Broiler. Pustaka Larasan, Denpasar, Indonesia.
Youssef N., Sheik C.S., Krumholz L.R., Najar F.Z., Roe B.A. and Elshahed M.S. (2009). Comparison of species richness estimates obtained using nearly complete fragments and simulated pyrosequencing-generated fragments in 16S rRNA gene-based environmental surveys. Appl. Environ. Microbiol. 75, 5227-5236.
Zhang L.Y., Peng Q.Y., Liu Y.R., Ma Q.G., Zhang J.Y., Guo Y.P., Xue Z. and Zhao L.H. (2021). Effects of oregano essential oil as an antibiotic growth promoter alternative on growth performance, antioxidant status, and intestinal health of broilers. Poult. Sci. 100, 101163-101171.
Zhang Z.P., Shen C.C., Gao F.L., Wei H., Ren D.F. and Lu J. (2017). Isolation, purification and structural characterization of two novel water-soluble polysaccharides from anredera cordifolia. Molecules. 22, 1276-1283.