Psoriatic lesions are characterized by higher bacterial load and imbalance between Cutibacterium and Corynebacterium

银屑病 医学 棒状杆菌 微生物群 病理 皮肤病科 聚合酶链反应 细菌 生物 遗传学 基因
作者
Cheng Quan,Xiaoying Chen,Xia Li,Feng Xue,Lihong Chen,Na Liu,Bo Wang,Lanqi Wang,Xiaopan Wang,Hui Yang,Jie Zheng
出处
期刊:Journal of The American Academy of Dermatology [Elsevier BV]
卷期号:82 (4): 955-961 被引量:92
标识
DOI:10.1016/j.jaad.2019.06.024
摘要

Background Several studies have found that the microbiota of psoriatic lesions is different from that of healthy skin. Objective To characterize the microbiota of lesional and unaffected skin in patients with psoriasis and controls and investigate the correlation between cutaneous microbiota and clinical features of psoriasis. Methods Using quantitative polymerase chain reaction and 16S rRNA sequencing, we assayed the profiles of cutaneous microbiota in controls, unaffected skin, and psoriatic lesions. We also investigated the correlation of psoriasis-associated taxa with clinical characteristics. Results High bacterial load was identified in the psoriatic lesions compared with unaffected skin and controls. There was an imbalance between Cutibacterium (also known as Propionibacterium) and Corynebacterium in psoriatic skin. Lesions showed a higher proportion of Corynebacterium and a lower proportion of Cutibacterium compared with unaffected skin and controls. Corynebacterium was correlated with the severity of local lesions, whereas Cutibacterium showed correlation with the abnormity of skin capacitance. Limitations We did not conduct a longitudinal study. Conclusions Psoriatic lesions are characterized by higher bacterial load and imbalance between Cutibacterium and Corynebacterium. Several studies have found that the microbiota of psoriatic lesions is different from that of healthy skin. To characterize the microbiota of lesional and unaffected skin in patients with psoriasis and controls and investigate the correlation between cutaneous microbiota and clinical features of psoriasis. Using quantitative polymerase chain reaction and 16S rRNA sequencing, we assayed the profiles of cutaneous microbiota in controls, unaffected skin, and psoriatic lesions. We also investigated the correlation of psoriasis-associated taxa with clinical characteristics. High bacterial load was identified in the psoriatic lesions compared with unaffected skin and controls. There was an imbalance between Cutibacterium (also known as Propionibacterium) and Corynebacterium in psoriatic skin. Lesions showed a higher proportion of Corynebacterium and a lower proportion of Cutibacterium compared with unaffected skin and controls. Corynebacterium was correlated with the severity of local lesions, whereas Cutibacterium showed correlation with the abnormity of skin capacitance. We did not conduct a longitudinal study. Psoriatic lesions are characterized by higher bacterial load and imbalance between Cutibacterium and Corynebacterium.
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