Peritoneal Microbiome in End-Stage Renal Disease Patients and the Impact of Peritoneal Dialysis Therapy

被引:20
作者
Simoes-Silva, Liliana [1 ,2 ,3 ]
Araujo, Ricardo [1 ,2 ,4 ]
Pestana, Manuel [1 ,2 ,5 ,6 ]
Soares-Silva, Isabel [1 ,2 ,7 ]
Sampaio-Maia, Benedita [1 ,2 ,8 ]
机构
[1] Univ Porto, I3S, P-4200180 Porto, Portugal
[2] Univ Porto, INEB Inst Engn Biomed, Rua Alfredo Allen 208, P-4200180 Porto, Portugal
[3] Inst Politecn Castelo Branco, Escola Super Saude Dr Lopes Dias, P-6000767 Castelo Branco, Portugal
[4] Flinders Univ South Australia, Med Biotechnol, Bedford Pk, SA 5042, Australia
[5] Univ Porto, Fac Med, P-4200319 Porto, Portugal
[6] Ctr Hosp Univ Sao Joao, Dept Nephrol, EPE, P-4200319 Porto, Portugal
[7] Univ Minho, Ctr Mol & Environm Biol CBMA, Dept Biol, Campus Gualtar, P-4710057 Braga, Portugal
[8] Univ Porto, Fac Med Dent, P-4200393 Porto, Portugal
关键词
microbiome; peritoneum; chronic kidney disease; peritoneal dialysis; end-stage kidney disease; SIZED POLYETHYLENE-GLYCOLS; STAPHYLOCOCCUS-AUREUS; PSEUDOMONAS PERITONITIS; BLOOD MICROBIOME; BARRIER FUNCTION; GUT MICROBIOME; TIGHT JUNCTION; EXIT SITE; DIVERSITY; INFECTION;
D O I
10.3390/microorganisms8020173
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Factors influencing the occurrence of peritoneal dialysis (PD)-related infections are still far from fully understood. Recent studies described the existence of specific microbiomes in body sites previously considered microbiome-free, unravelling new microbial pathways in the human body. In the present study, we analyzed the peritoneum of end-stage kidney disease (ESKD) patients to determine if they harbored a specific microbiome and if it is altered in patients on PD therapy. We conducted a cross-sectional study where the peritoneal microbiomes from ESKD patients with intact peritoneal cavities (ESKD non-PD, n = 11) and ESKD patients undergoing PD therapy (ESKD PD, n = 9) were analyzed with a 16S rRNA approach. Peritoneal tissue of ESKD patients contained characteristically low-abundance microbiomes dominated by Proteobacteria, Firmicutes, Actinobacteria, and Bacteroidetes. Patients undergoing PD therapy presented lower species richness, with dominance by the Pseudomonadaceae and Prevotelaceae families. This study provides the first characterization of the peritoneal microbiome in ESKD patients, bringing new insight to the human microbiome. Additionally, PD therapy may induce changes in this unique microbiome. The clinical relevance of these observations should be further explored to uncover the role of the peritoneal microbiome as a key element in the onset or aggravation of infection in ESKD patients, especially those undergoing PD.
引用
收藏
页数:15
相关论文
共 69 条
[21]   A core microbiome associated with the peritoneal tumors of pseudomyxoma peritonei [J].
Gilbreath, Jeremy J. ;
Semino-Mora, Cristina ;
Friedline, Christopher J. ;
Liu, Hui ;
Bodi, Kip L. ;
McAvoy, Thomas J. ;
Francis, Jennifer ;
Nieroda, Carol ;
Sardi, Armando ;
Dubois, Andre ;
Lazinski, David W. ;
Camilli, Andrew ;
Testerman, Traci L. ;
Merrell, D. Scott .
ORPHANET JOURNAL OF RARE DISEASES, 2013, 8
[22]   Risk factors for peritonitis in long-term peritoneal dialysis: The network 9 peritonitis and catheter survival studies [J].
Golper, TA ;
Brier, ME ;
Bunke, M ;
Schreiber, MJ ;
Bartlett, DK ;
Hamilton, RW ;
Strife, F ;
Hamburger, RJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 28 (03) :428-436
[23]   Topographical and Temporal Diversity of the Human Skin Microbiome [J].
Grice, Elizabeth A. ;
Kong, Heidi H. ;
Conlan, Sean ;
Deming, Clayton B. ;
Davis, Joie ;
Young, Alice C. ;
Bouffard, Gerard G. ;
Blakesley, Robert W. ;
Murray, Patrick R. ;
Green, Eric D. ;
Turner, Maria L. ;
Segre, Julia A. .
SCIENCE, 2009, 324 (5931) :1190-1192
[24]   Peritonitis associated with exit site and tunnel infections [J].
Gupta, B ;
Bernardini, J ;
Piraino, B .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 28 (03) :415-419
[25]   Intestinal Microbiota Is Influenced by Gender and Body Mass Index [J].
Haro, Carmen ;
Rangel-Zuniga, Oriol A. ;
Alcala-Diaz, Juan F. ;
Gomez-Delgado, Francisco ;
Perez-Martinez, Pablo ;
Delgado-Lista, Javier ;
Quintana-Navarro, Gracia M. ;
Landa, Blanca B. ;
Navas-Cortes, Juan A. ;
Tena-Sempere, Manuel ;
Clemente, Jose C. ;
Lopez-Miranda, Jose ;
Perez-Jimenez, Francisco ;
Camargo, Antonio .
PLOS ONE, 2016, 11 (05)
[26]   Staphylococcus aureus induces caspase-independent cell death in human peritoneal mesothelial cells [J].
Haslinger-Loeffler, B. ;
Wagner, B. ;
Brueck, M. ;
Strangfeld, K. ;
Grundmeier, M. ;
Fischer, U. ;
Voelker, W. ;
Peters, G. ;
Schulze-Osthoff, K. ;
Sinha, B. .
KIDNEY INTERNATIONAL, 2006, 70 (06) :1089-1098
[27]   Inhibition of the accumulation of uremic toxins in the blood and their precursors in the feces after oral administration of Lebinin(R), a lactic acid bacteria preparation, to uremic patients undergoing hemodialysis [J].
Hida, M ;
Aiba, Y ;
Sawamura, S ;
Suzuki, N ;
Satoh, T ;
Koga, Y .
NEPHRON, 1996, 74 (02) :349-355
[28]   The Microbiome of Aseptically Collected Human Breast Tissue in Benign and Malignant Disease [J].
Hieken, Tina J. ;
Chen, Jun ;
Hoskin, Tanya L. ;
Walther-Antonio, Marina ;
Johnson, Stephen ;
Ramaker, Sheri ;
Xiao, Jian ;
Radisky, Derek C. ;
Knutson, Keith L. ;
Kalari, Krishna R. ;
Yao, Janet Z. ;
Baddour, Larry M. ;
Chia, Nicholas ;
Degnim, Amy C. .
SCIENTIFIC REPORTS, 2016, 6
[29]   Global Prevalence of Chronic Kidney Disease - A Systematic Review and Meta-Analysis [J].
Hill, Nathan R. ;
Fatoba, Samuel T. ;
Oke, Jason L. ;
Hirst, Jennifer A. ;
O'Callaghan, Christopher A. ;
Lasserson, Daniel S. ;
Hobbs, F. D. Richard .
PLOS ONE, 2016, 11 (07)
[30]  
Holodniy M, 2011, PLOS ONE, V6, DOI [10.1371/journal.pone.0014764, 10.1371/journal.pone.0025792]