特应性皮炎患者上呼吸道分泌物及结肠内容物培养的评价

A. Zhestkov, A. Lyamin, O. O. Pobezhimova
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When seeding feces patients from all groups, statistically significant differences were revealed for the following microorganisms, depending on the severity: Enterococcus faecium (61%), Streptococcus anginosus (16.7%), Parabacteroides distasonis (22.2%) were found in remission; at the stage of exacerbation with exacerbation of atopic dermatitis in the form of a limited form - Enterococcus faecalis (39.3%), Lactobacillus fermentum (16.1%), Streptococcus parasanguinis (9%);with a common form of exacerbation, Klebsiella pneumonia (50%), Klebsiella oxytoca (50%), Enterococcus mundtii (16.7%), Echerichia vulneris (16.7%), Lactobacillus salivarius (83.3%), Raoultella ornithinolytica(16.7%), Enterococcus avium (50%), Enterobacter asburie (16.7%), Citr obacter braaki (33.3%), Bacteroides vulgates (33.3%), Bifidobacterium adolescentis(16.7%), Enterococcus durans (16.7%), Lactobacillus crispatus (16.7%), Corynebacterium amycolatum (33.3%), Streptococcus sanguinis (16.7%). Inoculation of oropharyngeal discharge from patients with atopic dermatitis revealed statistically significant differences for the following microorganisms, depending on the severity: Streptococcus australis (11.1%) was detected in remission; in the stage of exacerbation with a limited form of atopic dermatitis, Rothia mucalaginosa (19.6%), Streptococcus saliverius (39.3%) were identified; in the stage of exacerbation with a widespread form of atopic dermatitis, Streptococcus anginosus (16.7%;), Candida albicans (33.3%), Streptococcus gordonii (16.7%), Staphylococcus haemolyticus (16.7%), Neisseria oralis (33.3%), Corynebacterium amycolatum (16.7%), Kocuria rhizophila (33.3%), Lactobacillus rhamnosus (16.7%). 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引用次数: 0

摘要

的目标。本研究的目的是研究特应性皮炎患者鼻、口咽部分泌物和结肠内容物中微生物群落的种类多样性。材料和方法。该研究包括80名患有特应性皮炎的患者。根据AD的严重程度将患者分为3组(重点关注SCORAD量表)。患者接受了口腔、鼻腔和肠道的生物材料采集。该材料的播种是在一份扩展的营养介质清单上进行的。通过Microflex LT (Bruker, Germany)上的MALDI-ToF质谱分析,可以通过甲酸直接沉积和延长沉积来识别所得微生物。结果和讨论。各组患者播种粪便时,根据严重程度不同,微生物数量差异有统计学意义:粪肠球菌(61%)、心绞痛链球菌(16.7%)、副芽孢杆菌(22.2%)缓解;在特应性皮炎加重阶段,以有限形式出现的粪肠球菌(39.3%)、发酵乳杆菌(16.1%)、副血链球菌(9%);常见加重形式有肺炎克雷伯菌(50%)、氧化克雷伯菌(50%)、蒙氏肠球菌(16.7%)、易损埃希菌(16.7%)、唾液乳杆菌(83.3%)、溶鸟拉乌尔氏菌(16.7%)、鸟肠球菌(50%)、阿斯伯里肠杆菌(16.7%)、布拉基柠檬酸杆菌(33.3%)、普通拟杆菌(33.3%)、青少年双歧杆菌(16.7%)、durans肠球菌(16.7%)、crispatus乳杆菌(16.7%)、amycolatum棒状杆菌(33.3%)、sanguincoccus(16.7%)。对特应性皮炎患者口咽分泌物进行接种,根据不同的严重程度,发现以下微生物有统计学差异:缓解期检出南链球菌(11.1%);加重期伴有局限性特应性皮炎,检出粘膜罗氏菌(19.6%)、唾液链球菌(39.3%);加重期以广泛形式的特应性皮炎为主:血管链球菌(16.7%)、白色念珠菌(33.3%)、戈多氏链球菌(16.7%)、溶血葡萄球菌(16.7%)、口腔奈瑟菌(33.3%)、淀粉状棒状杆菌(16.7%)、嗜根Kocuria(33.3%)、鼠李糖乳杆菌(16.7%)。对特应性皮炎患者的鼻分泌物进行接种,根据不同的严重程度,以下微生物的差异有统计学意义:溶血葡萄球菌(16.7%)、芦丁葡萄球菌(11.1%)、黄连葡萄球菌(11.1%)缓解。在恶化阶段,广泛存在特应性皮炎,奇异变形杆菌(16.7%),前庭链球菌(16.7%),sobrincoccus (16.7%), warneri葡萄球菌(16.7%),coyle棒状杆菌(16.7%),植物乳杆菌(16.7%)。结论。我们的研究结果表明,在特应性皮炎患者中,酶缺乏和微生物群的定性组成发生了显著变化,这违反了身体的免疫调节功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF CULTUROMA OF THE DISCHARGE OF THE UPPER RESPIRATORY TRACT AND THE CONTENTS OF THE COLON IN PATIENTS WITH ATOPIC DERMATITIS
Aim. The aim of the study is to study the species diversity of the microflora of the discharge of the nose, oropharynx and the contents of the colon in atopic dermatitis. Material and methods. The study included 80 patients with atopic dermatitis. Patients are divided into 3 groups depending on the severity of AD (Focusing on the SCORAD scale). The patients underwent collection of biomaterials from the oral and nasal cavities and intestines. Sowing of the material was carried out on an extended list of nutrient media. As a result of the MALDI-ToF mass spectrometry on the Microflex LT (Bruker, Germany), the resulting microorganisms were recognized by direct and extended deposition using formic acid. Results and discussion. When seeding feces patients from all groups, statistically significant differences were revealed for the following microorganisms, depending on the severity: Enterococcus faecium (61%), Streptococcus anginosus (16.7%), Parabacteroides distasonis (22.2%) were found in remission; at the stage of exacerbation with exacerbation of atopic dermatitis in the form of a limited form - Enterococcus faecalis (39.3%), Lactobacillus fermentum (16.1%), Streptococcus parasanguinis (9%);with a common form of exacerbation, Klebsiella pneumonia (50%), Klebsiella oxytoca (50%), Enterococcus mundtii (16.7%), Echerichia vulneris (16.7%), Lactobacillus salivarius (83.3%), Raoultella ornithinolytica(16.7%), Enterococcus avium (50%), Enterobacter asburie (16.7%), Citr obacter braaki (33.3%), Bacteroides vulgates (33.3%), Bifidobacterium adolescentis(16.7%), Enterococcus durans (16.7%), Lactobacillus crispatus (16.7%), Corynebacterium amycolatum (33.3%), Streptococcus sanguinis (16.7%). Inoculation of oropharyngeal discharge from patients with atopic dermatitis revealed statistically significant differences for the following microorganisms, depending on the severity: Streptococcus australis (11.1%) was detected in remission; in the stage of exacerbation with a limited form of atopic dermatitis, Rothia mucalaginosa (19.6%), Streptococcus saliverius (39.3%) were identified; in the stage of exacerbation with a widespread form of atopic dermatitis, Streptococcus anginosus (16.7%;), Candida albicans (33.3%), Streptococcus gordonii (16.7%), Staphylococcus haemolyticus (16.7%), Neisseria oralis (33.3%), Corynebacterium amycolatum (16.7%), Kocuria rhizophila (33.3%), Lactobacillus rhamnosus (16.7%). Inoculation of nasal discharge from patients with atopic dermatitis revealed statistically significant differences for the following microorganisms, depending on the severity: Staphylococcus haemolyticus (16.7%), Staphylococcus lugdunensis (11.1%), Staphylococcus copitis (11.1%) were found in remission. At the stage of exacerbation with a widespread form of atopic dermatitis, Proteus mirabilis (16.7%), Streptococcus vestibularis (16.7%), Streptococcus sobrinus (16.7%), Staphylococcus warneri (16.7%), Corynebacterium coyleae (16.7%), Lactobacillus plantarum (16.7%). Conclusion. Our results indicate enzymatic deficiency and significant changes in the qualitative composition of the microbiota in people with atopic dermatitis, which violates the body's immunomodulating function.
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