耐多药结核病hiv感染者的肠道菌群

L. Otdushkina, Y. Zakharova, A. A. Kholodov, L. A. Levanova, T. V. Pyanzova, A. Markovskaya
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Gut microbiota of patients with multidrug-resistant tuberculosis was consistently represented by Bifidobacterium spp., Lactobacillus spp., Enterococcus spp., Escherichia spp., Staphylococcus spp., and Candida regardless of theirHIV status. Species composition and prevalence of virulence factors in Staphylococcus spp. and fungi isolated from patients with multidrug-resistant tuberculosis also did not depend on HIV status. Complementary microorganisms were represented exclusively by Clostridium spp., while random microbiota was represented by 6 genera (Enterobacter spp., Citrobacter spp., Salmonella spp., Klebsiella spp., Proteus spp., and Pseudomonas spp.) belonging to the Proteobacteria phylum.Conclusion. 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摘要

的目标。目的:确定hiv感染肺结核患者肠道菌群的组成和特性。材料与方法。我们研究了92份来自肺结核患者(n = 46)和肺结核合并HIV感染患者(n = 46)的粪便样本,并对细菌的外观、培养特性和生化特征进行了以下检查。采用Dazho-Odum指标测定微生物类群的稳定性。在C > 50%时,微生物被分类为恒定的,在25% < C < 50%时,微生物被分类为互补的,在C < 25%时,微生物被分类为偶然的。耐多药结核病患者的肠道菌群始终以双歧杆菌、乳杆菌、肠球菌、埃希氏菌、葡萄球菌和念珠菌为代表,与hiv感染状态无关。从耐多药结核病患者中分离的葡萄球菌和真菌的种类组成和毒力因子的流行率也不依赖于HIV状态。互补菌群以梭状芽胞杆菌(Clostridium spp)为代表,随机菌群为6属(Enterobacter spp., Citrobacter spp., Salmonella spp., Klebsiella spp., Proteus spp., Pseudomonas spp.),属于变形菌门。hiv阳性和hiv阴性多药耐药结核病患者肠道菌群组成相似,表明肠道生态失调的共同机制和纠正方法是统一的。
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Gut microbiota of HIV-infected patients with multidrug-resistant tuberculosis
Aim. To determine the composition and properties of the gut microbiota in HIV-infected patients with pulmonary tuberculosis.Materials and Methods. We studied 92 faecal samples from patients with pulmonary tuberculosis (n = 46) and patients with combined pulmonary tuberculosis and HIV infection (n = 46), with the following examination of the appearance, cultural properties, and biochemical profile of the bacteria. The constancy of microbial taxa was determined using Dazho-Odum indicator. Microorganisms were classified as constant at C > 50%, as complementary at 25% < C < 50% and as occasional at C < 25%.Results. Gut microbiota of patients with multidrug-resistant tuberculosis was consistently represented by Bifidobacterium spp., Lactobacillus spp., Enterococcus spp., Escherichia spp., Staphylococcus spp., and Candida regardless of theirHIV status. Species composition and prevalence of virulence factors in Staphylococcus spp. and fungi isolated from patients with multidrug-resistant tuberculosis also did not depend on HIV status. Complementary microorganisms were represented exclusively by Clostridium spp., while random microbiota was represented by 6 genera (Enterobacter spp., Citrobacter spp., Salmonella spp., Klebsiella spp., Proteus spp., and Pseudomonas spp.) belonging to the Proteobacteria phylum.Conclusion. Similar composition of gut microbiota in HIV-positive and HIV-negative patients with multidrug-resistant tuberculosis indicates common mechanisms of intestinal dysbiosis and a uniform approach for its correction.
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