Contributions to this study:post doctorate,Responsible for the 34 establishment, detection, analysis and quality control of the database of intestinal 35 flora structure and gene polymorphism) 36 37 Cuifeng Zhu, Jianguo Liu and Yong Pan contributed equally to this work. Author 38 order was determined on the basis of seniority. ( CuiFeng Zhu, Department 39 director of Dept of Clinical Nutrition, chief physician, master tutor of Shenzhen 40 hospital of southern medical university. Post doctor fellows of Dept of 41 endocrinology of university of Hong Kong & The State Key laboratory of 42 Pharmaceutical Biotechnology. E-mail :1794371266@qq.com(Contributions to 43 this study: chief physician of Nutrition department and post doctorate, responsible 44 for the design and implementation of this project, data collation and paper 45 writing); JianGuo Liu, Associate chief physician, Department director of Dept 46 of Health management of Shenzhen hospital of southern medical University. E-47 3 / 25 mail : JgLiu123@163.com(Contribution to this study: general practitioner at 48 health management center, responsible for case collection and data collation); , 13570469574 66 (Contribution to this study:Nutrition department attending physician, in 67 charge of the medical history of selected patients, menstrual history, life history 68 and other data survey) 69 4 / 25 Abstract 120 Background: Gut microbiota, mainly characterized by fecal bacterial 121 compositions, affects human immune system and pathophysiological 122 development. Our aim was to measure the quantitative differences of 123 fecal bacterial compositions between osteoporotic patients and healthy 124 subjects, and to identify novel bacterial taxa that speculate the 125 incidence of osteoporosis in female. 126 127 Method: We recruited 104 female subjects, including 45 osteoporotic 128 individuals and 59 healthy control. Fecal samples were collected for 129 further analysis by 16S rRNA quantitative arrays and bioinformatics 130 analysis. 131 132 Results: Analyses of α-and β-diversity demonstrated that the diversity 133 and composition of fecal bacterial compositions were both significant 134 different in osteoporosis group, as compared with healthy group. 135 Multiple bacterial genera were significantly increased (e.g., Roseburia 136 and Bacteroides) or decreased (e.g., Streptococcus and Dorea) in the 137 osteoporotic cases. Furthermore, the osteoporosiscould be efficiently 138