Yin Yue, Tuohutaerbieke Maermaer, Feng Chengjie, Li Xinjie, Zhang Yuqi, Xu Qiang, Tu Jing, Yang Ence, Zou Qinghua, Shen Tao
Department of Microbiology and Infectious Disease Center, School of Basic Medical Sciences, Peking University, Beijing 100191, China.
Department of Microbiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
Viruses. 2022 Aug 18;14(8):1811. doi: 10.3390/v14081811.
Intestinal mycobiome dysbiosis plays an important role in the advancement of HIV- and HCV-infected patients. Co-infection with HCV is an important risk factor for exacerbating immune activation in HIV-infected patients, and gut fungal microbial dysbiosis plays an important role. However, no systematic study has been conducted on the intestinal fungal microbiome of HIV/HCV co-infected patients to date. Patients infected with HIV and HCV, either alone or in combination, and healthy volunteers were included. Stool samples were collected for fungal ITS sequencing and for further mycobiome statistical analysis. We found that the abundance of fungal species significantly decreased in the HIV/HCV co-infection group compared to in the healthy control group, while no significant differences were found in the mono-infection groups. Low-CD4 + T-cell patients in the HIV group and high-ALT-level patients in the HCV group were discovered to have a more chaotic fungal community. Furthermore, the opportunistic pathogenic fungal profiles and fungal inter-correlations in the co-infection group became less characteristic but more complicated than those in the mono-infection groups. Intestinal fungal dysregulation occurs in HIV- and HCV-infected patients, and this dysregulation is further complicated in HIV/HCV co-infected patients.
肠道真菌微生物群失调在HIV和HCV感染患者病情进展中起重要作用。合并感染HCV是加剧HIV感染患者免疫激活的一个重要危险因素,而肠道真菌微生物群失调起重要作用。然而,迄今为止尚未对HIV/HCV合并感染患者的肠道真菌微生物群进行系统研究。纳入单独感染HIV或HCV以及合并感染HIV和HCV的患者,以及健康志愿者。收集粪便样本进行真菌ITS测序和进一步的真菌微生物群统计分析。我们发现,与健康对照组相比,HIV/HCV合并感染组的真菌种类丰度显著降低,而单一感染组未发现显著差异。发现HIV组中CD4 + T细胞水平低的患者和HCV组中ALT水平高的患者真菌群落更紊乱。此外,合并感染组的机会性致病真菌谱和真菌相互关系比单一感染组的特征性更弱但更复杂。HIV和HCV感染患者存在肠道真菌调节异常,而这种调节异常在HIV/HCV合并感染患者中进一步复杂化。