Original articles

The structure of gut microbiome in idiopathic short stature profiled by 16S rRNA second generation sequencing sequencing

Expand
  • Department of Pediatrics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

Received date: 2020-10-13

  Online published: 2022-06-28

Abstract

Objective: To investigate structural characteristics of gut microbiome in idiopathic short stature (ISS) children and difference in gut microbiome between ISS and healthy children(HC) children, so as to explore the possible mechanism of action of gut microbiome on ISS. Methods: A total of 16 children aging from 4 to 8, including 16 ISS children (ISS group)and 16 HC (control group) were enrolled in the study. Flora of the collected feces were collected, and V3-V4 of bacterial 16S rRNA was sequenced with high-throughput sequencing. Diversity and abundance of gut microbiome between HC and ISS group were compared. Results: The structure of gut microbiome in ISS children were significantly different from HC children. The Chao1 (diversity index) of ISS group were lower than that of HC group (1109.85±435.23 vs. 1485.68±334.51) (P=0.018) as well as Observed_species index(946.98±374.93 vs. 1 217.69±289.66)(P=0.038), indicating decreased relative abundance of gut microbiome in ISS group. It’s also showed that the relative abundances of Faecalibacterium and Eubacterium were significantly lower in ISS group than HC group (P<0.05). In ISS group, both abundances of Faecalibacterium and Eubacterium were positively correlated with height-SDS and insulin-like growth factor 1(IGF1)-SDS(r>0.6, P<0.05). Conclusions: For ISS, the abundance of gut microbiome decreases and the flora also experiences significant structural changes. Faecalibacterium and Eubacterium may decrease IGF-1 by short-chain fatty acid (SCFA), constituting a possible pathogenic mechanism for ISS.

Cite this article

LI Lin, AN Jingjing, WANG Junqi, WANG Xinqiong, DONG Zhiya . The structure of gut microbiome in idiopathic short stature profiled by 16S rRNA second generation sequencing sequencing[J]. Journal of Diagnostics Concepts & Practice, 2021 , 20(02) : 149 -154 . DOI: 10.16150/j.1671-2870.2021.02.006

References

[1] Lindsay R, Feldkamp M, Harris D, et al. Utah growth study: growth standards and the prevalence of growth hormone deficiency[J]. J Pediatr, 1994, 125(1):29-35.
[2] Chassaing B, Aitken JD, Gewirtz AT, et al. Gut microbiota drives metabolic disease in immunologically altered mice[J]. Adv Immunol, 2012, 116:93-112.
[3] Kane AV, Dinh DM, Ward HD. Childhood malnutrition and the intestinal microbiome[J]. Pediatr Res, 2015, 77(1-2):256-262.
[4] Kostic AD, Xavier RJ, Gevers D. The microbiome in inflammatory bowel disease: current status and the future ahead[J]. Gastroenterology, 2014, 146(6):1489-1499.
[5] Turnbaugh PJ, Ley RE, Mahowald MA, et al. An obesity-associated gut microbiome with increased capacity for energy harvest[J]. Nature, 2006, 444(7122):1027-1031.
[6] Wang Y, Kasper LH. The role of microbiome in central nervous system disorders[J]. Brain Behav Immun, 2014, 38:1-12.
[7] Storelli G, Defaye A, Erkosar B, et al. Lactobacillus plantarum promotes drosophila systemic growth by modulating hormonal signals through TOR-dependent nutrient sensing[J]. Cell Metab, 2011, 14(3):403-414.
[8] Avella MA, Place A, Du SJ, et al. Lactobacillus rhamnosus accelerates zebrafish backbone calcification and gonadal differentiation through effects on the GnRH and IGF systems[J]. PLoS One, 2012, 7(9):e45572.
[9] Kareem KY, Loh TC, Foo HL, et al. Effects of dietary postbiotic and inulin on growth performance, IGF1 and GHR mRNA expression, faecal microbiota and volatile fatty acids in broilers[J]. BMC Vet Res, 2016, 12(1):163.
[10] 李辉, 季成叶, 宗心南, 等. 中国0-18岁儿童、青少年体块指数的生长曲线[J]. 中华儿科杂志, 2009, 47(7):493-498.
[11] Isojima T, Shimatsu A, Yokoya S, et al. Standardized centile curves and reference intervals of serum insulin-like growth factor-I(IGF-I) levels in a normal Japanese population using the LMS method[J]. Endocr J, 2012, 59(9):771-780.
[12] Shin SC, Kim SH, You H, et al. Drosophila microbiome modulates host developmental and metabolic homeostasis via insulin signaling[J]. Science, 2011, 334(6056):670-674.
[13] Schwarzer M, Strigini M, Leulier F. Gut Microbiota and Host Juvenile Growth[J]. Calcif Tissue Int, 2018, 102(4):387-405.
[14] Smith PM, Howitt MR, Panikov N, et al. The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis[J]. Science, 2013, 341(6145):569-573.
[15] Yan J, Herzog JW, Tsang K, et al. Gut microbiota induce IGF-1 and promote bone formation and growth[J]. Proc Natl Acad Sci USA, 2016, 113(47):E7554-E7563.
[16] Hustoft TN, Hausken T, Ystad SO, et al. Effects of va-rying dietary content of fermentable short-chain carbohydrates on symptoms, fecal microenvironment, and cytokine profiles in patients with irritable bowel syndrome[J/OL]. Neurogastroenterol Motil, 2016-10-16[2020-10-13]. https://pubmed.ncbi.nlm.nih.gov/27747984/.
[17] Louis P, Flint HJ. Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine[J]. FEMS Microbiol Lett, 2009, 294(1):1-8.
Outlines

/