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Molecular characterization of skin microbiota between cancer cachexia patients and healthy volunteers.

Authors :
Li W
Han L
Yu P
Ma C
Wu X
Moore JE
Xu J
Source :
Microbial ecology [Microb Ecol] 2014 Apr; Vol. 67 (3), pp. 679-89. Date of Electronic Publication: 2014 Jan 09.
Publication Year :
2014

Abstract

Systemic inflammation contributes to both the development of cancer and of cachexia. The microenvironment of bacterial habitats might be changed during the progression of cancer cachexia. The aim of this study was to quantitatively and qualitatively compare the composition of the skin microbiota between cancer cachexia patients and healthy volunteers. Cutaneous bacteria were swabbed at the axillary fossa of 70 cancer cachexia patients and 34 healthy individuals from China. Nested-PCR-denaturing gradient gel electrophoresis (PCR-DGGE) with primers specifically targeting V3 region and quantitative PCR (qPCR) for total bacteria, Corynebacterium spp., Staphylococcus spp., and Staphylococcus epidermidis were performed on all samples. Barcoded 454 pyrosequencing of the V3-V4 regions was performed on 30 randomly selected samples. By comparing diversity and richness indices, we found that the skin microbiome of cachectic cancer patients is less diverse than that of healthy participants, though these differences were not significant. The main microbes that reside on human skin were divided into four phyla: Firmicutes, Actinobacteria, Proteobacteria, and Bacteroidetes. Staphylococcus spp. and Corynebacterium spp. were the dominant bacteria at the genus level. Significantly fewer Corynebacterium spp. had been observed in cachexia patients compared to healthy subjects. These results suggest that the presence of cancer and cachexia alters human skin bacterial communities. Understanding the changes in microbiota during cancer cachexia may lead to new insights into the syndrome.

Details

Language :
English
ISSN :
1432-184X
Volume :
67
Issue :
3
Database :
MEDLINE
Journal :
Microbial ecology
Publication Type :
Academic Journal
Accession number :
24402361
Full Text :
https://doi.org/10.1007/s00248-013-0345-6