Molecular Nutrition

Intestinal Archaea Community Structure Analysis of Mice Transplanted with Jinhua and Landrace Pig Feces

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  • 1. Institute of Quality and Standard for Agro-Products, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China;
    2. Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing 100193, China;
    3. College of Animal Science and Technology, China Agricultural University, Beijing 100193, China

Received date: 2016-12-01

  Online published: 2017-06-07

Abstract

This experiment was conducted to explore the differences of the intestinal archaea community structures between the obese breed Jinhua pig and the lean breed Landrace pig, and to investigate the changes of the archaea community structure during the inter-species fecal microbiota transplantation (FMT). The fresh feces of Jinhua and Landrace pigs were collected and introduced into broad spectrum antibiotics treated germ-free mice guts by gavage, respectively. The total genomic DNA was extracted from the pig fecal samples and the transplanted mice cecal contents, and was used as templates to amplify the V4 region of the 16S rRNA gene by PCR with the universal primers of archaea. The PCR products were then subjected to high-throughput sequencing on an Illumina HiSeq sequencing platform. The obtained sequences were subsequently processed and analyzed with a series of software such as QⅡME. The results showed as follows:at the phylum level, three main phyla of archaea, Thaumarchaeota, Euryarchaeota, and Crenarchaeota, were found in pig fecal samples and transplanted mice cecal contents, with Thaumarchaeota as the dominant phylum; while at the genus level, five known genera of archaea were observed, with Cenarchaeum as the dominant genus. The abundance of phylum Euryarchaeota in Jinhua pig's feces was higher than that in Landrace pig's feces. Thaumarchaeota dominate the archaea community structure of transplanted mice cecal contents, with abundance of more than 70%, and Thaumarchaeota mainly consisted of Cenarchaeum. It was observed that no significant difference was exhibited between the two groups of mice at the phylum and genus levels (P>0.05), but the operational taxonomic unit (OTU) based principal coordinate analysis showed a good aggregation within each group. It is concluded that genus Cenarchaeum of phylum Thaumarchaeota is the dominant archaea in feces of Jinhua and Landrace pigs and cecal contents of mice recipients. Phylum Euryarchaeota is more abundant in Jinhua pig's feces than in Landrace pig's feces, and there is difference in archaea community structures between their respective mice recipients at the OTU level.

Cite this article

XIAO Yingping, WANG Junjun, LI Tiantian, TANG Biao, HE Xiangxiang, LI Kaifeng, YANG Hua . Intestinal Archaea Community Structure Analysis of Mice Transplanted with Jinhua and Landrace Pig Feces[J]. Chinese Journal of Animal Nutrition, 2017 , 29(6) : 1895 -1903 . DOI: 10.3969/j.issn.1006-267x.2017.06.010

References

[1] MIAO Z G,WANG L J,XU Z R,et al.Developmental changes of carcass composition,meat quality and organs in the Jinhua pig and Landrace[J].Animal,2009,3(3):468-473.  

[2] GUO J,SHAN T,WU T,et al.Comparisons of different muscle metabolic enzymes and muscle fiber types in Jinhua and Landrace pigs[J].Journal of Animal Science,2011,89(1):185-191.  

[3] HARTSTRA A V,BOUTER K E,BÄCKHED F,et al.Insights into the role of the microbiome in obesity and type 2 diabetes[J].Diabetes Care,2015,38(1):159-165.  

[4] KONTUREK P C,HAZIRI D,BRZOZOWSKI T,et al.Emerging role of fecal microbiota therapy in the treatment of gastrointestinal and extra-gastrointestinal diseases[J].Journal of Physiology and Pharmacology,2015,66(4):483-491.

[5] EME L,DOOLITTLE W F.Archaea[J].Current Biology,2015,25(19):R851-R855.

[6] GRIBALDO S,BROCHIER-ARMANET C.The origin and evolution of Archaea:a state of the art[J].Philosophical Transactions of the Royal Society of London.Series B:Biological Sciences,2006,361(1470):1007-1022.  

[7] LUO Y H,SU Y,WRIGHT A D,et al.Lean breed Landrace pigs harbor fecal methanogens at higher diversity and density than obese breed Erhualian pigs[J].Archaea,2012,2012:605289.

[8] SAMUEL B S,GORDON J I.A humanized gnotobiotic mouse model of host-archaeal-bacterial mutualism[J].Proceedings of the National Academy of Sciences of the United States of America,2006,103(26):10011-10016.  

[9] SAMUEL B S,HANSEN E E,MANCHESTER J K,et al.Genomic and metabolic adaptations of Methanobrevibacter smithii to the human gut[J].Proceedings of the National Academy of Sciences of the United States of America,2007,104(25):10643-10648.  

[10] BROCHIER-ARMANET C,BOUSSAU B,GRIBALDO S,et al.Mesophilic Crenarchaeota:proposal for a third archaeal phylum,the Thaumarchaeota[J].Nature Reviews Microbiology,2008,6(3):245-252.  

[11] YOU J,DAS A,DOLAN E M,et al.Ammonia-oxidizing archaea involved in nitrogen removal[J].Water Research,2009,43(7):1801-1809.  

[12] PESTER M,SCHLEPER C,WAGNER M.The Thaumarchaeota:an emerging view of their phylogeny and ecophysiology[J].Current Opinion in Microbiology,2011,14(3):300-306.  

[13] SHI Y,HUANG Z,HAN S,et al.Phylogenetic diversity of Archaea in the intestinal tract of termites from different lineages[J].Journal of Basic Microbiology,2015,55(8):1021-1028.  

[14] LI G N,XIA X J,TANG W C,et al.Intestinal microecology associated with fluoride resistance capability of the silkworm (Bombyx mori L.)[J].Applied Microbiology and Biotechnology,2016,100(15):6715-6724.  

[15] LESZCZYSZYN J J,RADOMSKI M,LESZCZYSZYN A M.Intestinal microbiota transplant-current state of knowledge[J].Reumatologia,2016,54(1):24-28.

[16] BOJANOVA D P,BORDENSTEIN S R.Fecal transplants:what is being transferred?[J].PLoS Biology,2016,14(7):e1002503.

[17] TURNBAUGH P J,LEY R E,MAHOWALD M A,et al.An obesity-associated gut microbiome with increased capacity for energy harvest[J].Nature,2006,444(7122):1027-1031.  

[18] KULECKA M,PAZIEWSKA A,ZEBER-LUBECKA N,et al.Prolonged transfer of feces from the lean mice modulates gut microbiota in obese mice[J].Nutrition & Metabolism,2016,13:57.

[19] DIAO H,YAN H L,XIAO Y,et al.Intestinal microbiota could transfer host Gut characteristics from pigs to mice[J].BMC Microbiology,2016,16:238.

[20] RAWLS J F,MAHOWALD M A,LEY R E,et al.Reciprocal gut microbiota transplants from zebrafish and mice to germ-free recipients reveal host habitat selection[J].Cell,2006,127(2):423-433.  

[21] MCFALL-NGAI M.Love the one you're with:vertebrate guts shape their microbiota[J].Cell,2006,127(2):247-249.  

[22] WANG Z N,KLIPFELL E,BENNETT B J,et al.Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease[J].Nature,2011,472(7341):57-63.  

[23] PANG X Y,HUA X G,YANG Q,et al.Inter-species transplantation of gut microbiota from human to pigs[J].The ISME Journal,2007,1(2):156-162.  

[24] CAPORASO J G,KUCZYNSKI J,STOMBAUGH J,et al.QⅡME allows analysis of high-throughput community sequencing data[J].Nature Methods,2010,7(5):335-336.  

[25] BOKULICH N A,SUBRAMANIAN S,FAITH J J,et al.Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing[J].Nature Methods,2013,10(1):57-59.

[26] EDGAR R C,HAAS B J,CLEMENTE J C,et al.UCHIME improves sensitivity and speed of chimera detection[J].Bioinformatics,2011,27(16):2194-2200.  

[27] HAAS B J,GEVERS D,EARL A M,et al.Chimeric 16S rRNA sequence formation and detection in Sanger and 454-pyrosequenced PCR amplicons[J].Genome Research,2011,21(3):494-504.  

[28] EDGAR R C.UPARSE:highly accurate OTU sequences from microbial amplicon reads[J].Nature Methods,2013,10(10):996-998.  

[29] ZHANG H,DIBAISE J K,ZUCCOLO A,et al.Human gut microbiota in obesity and after gastric bypass[J].Proceedings of the National Academy of Sciences of the United States of America,2009,106(7):2365-2370.  

[30] GACI N,BORREL G,TOTTEY W,et al.Archaea and the human gut:new beginning of an old story[J].World Journal of Gastroenterology,2014,20(43):16062-16078.  
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