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Fermentation of DaiDai fruit and its biological activity 傣傣果的发酵及其生物活性
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1443283
Xiangyu Meng, Nan Tang, Wenfeng Su, Weiji Chen, Yue Zhang, He Li
DaiDai fruit, a medicinal and edible plant fruit, is abundant in biologically active compounds and has a long history of use in traditional Chinese medicine. This research focuses on utilizing fermentation to develop a functional DaiDai fruit fermentation broth. Lactobacillus, Bacillus subtilis and Saccharomyces cerevisiae were employed in the fermentation process. By conducting screenings of bacterial strains, single factor experiments, and response surface methodology, the total flavonoids, polysaccharides, polyphenols, and 1,1-diphenyl-2-trinitrophenylhydrazine (DPPH) free radical scavenging rate were used as the index for selection, ultimately identifying Lactobacillus L-13 as the optimal fermentation strain. The optimal fermentation conditions were determined to be a time of 108 h, a temperature of 43.6°C, and a solid–liquid ratio of 1:15.157 (w/v). Under these conditions, the total flavonoid content reached 412.01 mg/g, representing a 36.71% increase compared to conventional extraction methods. The contents of polysaccharides and polyphenols and the DPPH scavenging rate were also increased. The fermentation broth of DaiDai fruit exhibited inhibitory effects on tyrosinase and melanin production in mouse melanoma cells B16-F10 induced by α-MSH and anti-inflammatory properties in a zebrafish inflammation model. These indicate that the DaiDai fruit fermentation broth possesses anti-melanoma, whitening, and anti-inflammatory properties, showcasing significant potential for applications in medicine, cosmetics, and other industries.
傣傣果是一种药食两用的植物果实,含有丰富的生物活性化合物,在传统中药中的应用历史悠久。本研究的重点是利用发酵技术开发功能性傣傣果发酵液。发酵过程中采用了乳酸杆菌、枯草芽孢杆菌和酵母菌。通过菌种筛选、单因素实验和响应面法,以总黄酮、多糖、多酚和 1,1-二苯基-2-三硝基苯肼(DPPH)自由基清除率作为筛选指标,最终确定乳酸杆菌 L-13 为最佳发酵菌株。最佳发酵条件被确定为:时间 108 小时,温度 43.6°C,固液比 1:15.157(w/v)。在此条件下,总黄酮含量达到 412.01 mg/g,比传统提取方法提高了 36.71%。多糖和多酚的含量以及 DPPH 清除率也有所提高。傣傣果发酵液对α-MSH 诱导的小鼠黑色素瘤细胞 B16-F10 的酪氨酸酶和黑色素生成有抑制作用,对斑马鱼炎症模型有抗炎作用。这表明,傣傣果发酵液具有抗黑色素瘤、美白和抗炎的特性,在医药、化妆品和其他行业的应用潜力巨大。
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引用次数: 0
The influence of benzene on the composition, diversity and performance of the anodic bacterial community in glucose-fed microbial fuel cells 苯对葡萄糖馈入微生物燃料电池中阳极细菌群落的组成、多样性和性能的影响
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1384463
Natalia Tyszkiewicz, J. Truu, Piotr Młynarz, Grzegorz Pasternak
Bioelectrochemical systems offer unique opportunities to remove recalcitrant environmental pollutants in a net positive energy process, although it remains challenging because of the toxic character of such compounds. In this study, microbial fuel cell (MFC) technology was applied to investigate the benzene degradation process for more than 160 days, where glucose was used as a co-metabolite and a control. We have applied an inoculation strategy that led to the development of 10 individual microbial communities. The electrochemical dynamics of MFC efficiency was observed, along with their 1H NMR metabolic fingerprints and analysis of the microbial community. The highest power density of 120 mW/m2 was recorded in the final period of the experiment when benzene/glucose was used as fuel. This is the highest value reported in a benzene/co-substrate system. Metabolite analysis confirmed the full removal of benzene, while the dominance of fermentation products indicated the strong occurrence of non-electrogenic reactions. Based on 16S rRNA gene amplicon sequencing, bacterial community analysis revealed several petroleum-degrading microorganisms, electroactive species and biosurfactant producers. The dominant species were recognised as Citrobacter freundii and Arcobacter faecis. Strong, positive impact of the presence of benzene on the alpha diversity was recorded, underlining the high complexity of the bioelectrochemically supported degradation of petroleum compounds. This study reveals the importance of supporting the bioelectrochemical degradation process with auxiliary substrates and inoculation strategies that allow the communities to reach sufficient diversity to improve the power output and degradation efficiency in MFCs beyond the previously known limits. This study, for the first time, provides an outlook on the syntrophic activity of biosurfactant producers and petroleum degraders towards the efficient removal and conversion of recalcitrant hydrophobic compounds into electricity in MFCs.
生物电化学系统为在净正能量过程中去除难降解的环境污染物提供了独特的机会,但由于此类化合物的毒性,这一过程仍具有挑战性。在这项研究中,我们应用微生物燃料电池(MFC)技术研究了超过 160 天的苯降解过程,其中使用葡萄糖作为辅助代谢物和对照。我们采用了接种策略,培养出了 10 个独立的微生物群落。在观察 MFC 效率的电化学动态的同时,还对它们的 1H NMR 代谢指纹和微生物群落进行了分析。在实验的最后阶段,当使用苯/葡萄糖作为燃料时,记录到的最高功率密度为 120 mW/m2。这是苯/共底物系统中报告的最高值。代谢物分析证实苯被完全去除,而发酵产物占主导地位则表明非电反应的发生率很高。根据 16S rRNA 基因扩增片段测序,细菌群落分析揭示了几种石油降解微生物、电活性物种和生物表面活性剂生产者。其中的优势菌种被确认为自由柠檬酸杆菌(Citrobacter freundii)和粪弧菌(Arcobacter faecis)。苯的存在对α多样性产生了强烈的积极影响,凸显了石油化合物生物电化学降解的高度复杂性。这项研究揭示了利用辅助基质和接种策略支持生物电化学降解过程的重要性,这些策略可使生物群落达到足够的多样性,从而提高 MFC 的功率输出和降解效率,使其超过之前已知的极限。这项研究首次展望了生物表面活性剂生产者和石油降解者在 MFCs 中高效去除难降解疏水化合物并将其转化为电能的合成活动。
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引用次数: 0
Soil phosphorus cycling microbial functional genes of monoculture and mixed plantations of native tree species in subtropical China 中国亚热带乡土树种单一种植和混合种植的土壤磷循环微生物功能基因
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1419645
Lin Qin, Zhirou Xiao, Angang Ming, Jinqian Teng, Hao Zhu, Jiaqi Qin, Zeli Liang
Transforming coniferous plantation into broadleaved or mixed broadleaved-coniferous plantations is the tendency of forest management strategies in subtropical China. However, the effects of this conversion on soil phosphorus (P) cycling microbial functional genes are still unknown.Soil samples were collected from 0–20, 20–40, and 40–60 cm (topsoil, middle layer, and subsoil, respectively) under coniferous Pinus massoniana (PM), broadleaved Erythrophleum fordii (EF), and their mixed (PM/EF) plantation in subtropical China. Used metagenomic sequencing to examine the alterations of relative abundances and molecular ecological network structure of soil P-cycling functional genes after the conversion of plantations.The composition of P-cycling genes in the topsoil of PM stand was significantly different from that of PM/EF and EF stands (p < 0.05), and total phosphorus (TP) was the main factor causing this difference. After transforming PM plantation into EF plantation, the relative abundances of P solubilization and mineralization genes significantly increased in the topsoil and middle layer with the decrease of soil TP content. The abundances of P-starvation response regulation genes also significantly increased in the subsoil (p < 0.05), which may have been influenced by soil organic carbon (SOC). The dominant genes in all soil layers under three plantations were phoR, glpP, gcd, ppk, and ppx. Transforming PM into EF plantation apparently increased gcd abundance in the topsoil (p < 0.05), with TP and NO3−-N being the main influencing factors. After transforming PM into PM/EF plantations, the molecular ecological network structure of P-cycling genes was more complex; moreover, the key genes in the network were modified with the transformation of PM plantation.Transforming PM into EF plantation mainly improved the phosphate solubilizing potential of microorganisms at topsoil, while transforming PM into PM/EF plantation may have enhanced structural stability of microbial P-cycling genes react to environmental changes.
将针叶林改造成阔叶林或阔叶林-针叶林混交林是中国亚热带森林经营战略的趋势。本研究采集了中国亚热带针叶林Pinus massoniana(PM)、阔叶林Erythrophleum fordii(EF)及其混交林(PM/EF)下0-20、20-40和40-60厘米(表土、中层和底土)的土壤样品。利用元基因组测序技术研究了种植园改造后土壤P循环功能基因相对丰度和分子生态网络结构的变化。PM种植园表土中P循环基因的组成与PM/EF和EF种植园表土中P循环基因的组成有显著差异(p < 0.05),总磷(TP)是造成这种差异的主要因素。将 PM 种植区改造为 EF 种植区后,随着土壤 TP 含量的降低,表层和中层土壤中 P 溶解和矿化基因的相对丰度明显增加。底土中 P-饥饿响应调控基因的丰度也明显增加(p < 0.05),这可能受到土壤有机碳(SOC)的影响。将 PM 改造成 EF 后,表层土壤中 gcd 的丰度明显增加(p < 0.05),主要影响因素是 TP 和 NO3--N。将PM转化为PM/EF种植园后,P循环基因的分子生态网络结构更加复杂,而且网络中的关键基因也随着PM种植园的转化而发生了改变。
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引用次数: 0
Application of metagenomic next-generation sequencing in the etiological diagnosis of refractory pneumonia in children 元基因组新一代测序在儿童难治性肺炎病因诊断中的应用
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1357372
Ya-nan Wang, Yu-ting Wu, Ling Cao, Wen-quan Niu
Metagenomic next-generation sequencing (mNGS) was used to analyze the etiological distribution of refractory pneumonia in children. We compared its efficacy in pathogen diagnosis against traditional methods to provide a basis for clinical adjustment and treatment.A total of 60 children with refractory pneumonia treated at the Department of Respiratory Medicine, Children’s Hospital Affiliated with the Capital Institute of Paediatrics, from September 2019 to December 2021 were enrolled in this study. Clinical data (including sex, age, laboratory tests, complications, and discharge diagnosis) and lower respiratory tract specimens were collected, including bronchoalveolar lavage fluid (BALF), deep sputum, pleural effusion, lung abscess puncture fluid, traditional respiratory pathogens (culture, acid-fast staining, polymerase chain reaction, serological testing, etc.), and mNGS detection methods were used to determine the distribution of pathogens in children with refractory pneumonia and to compare the positive rate and diagnostic efficiency of mNGS and traditional pathogen detection for different types of pathogens.Among the 60 children with refractory pneumonia, 43 specimens were positive by mNGS, and 67 strains of pathogens were detected, including 20.90% (14 strains) of which were Mycoplasma pneumoniae, 11.94% (8 strains) were Streptococcus pneumoniae, 7.46% (5 strains) were cytomegalovirus, and 5.97% (4 strains) were Candida albicans. Thirty-nine strains of Mycoplasma pneumoniae (41.03%, 16 strains), Streptococcus pneumoniae (10.26%, 4 strains), Candida albicans (7.69%, 3 strains), and Aspergillus (5.13%, 2 strains) were detected using traditional methods. The positive rate of mNGS detection was 90.48%, and the positive rate of the traditional method was 61.90% (p = 0.050), especially for G+ bacteria. The positive rate of mNGS was greater than that of traditional methods (p < 0.05), but they had no significant difference in detecting G- bacteria, viruses, fungi, or Mycoplasma/Chlamydia. Among the 60 patients, 21 had mixed infections, 25 had single infections, and the other 14 had unknown pathogens. Mycoplasma pneumoniae was most common in both mixed infections and single infections. The sensitivity, specificity, positive predictive value, and negative predictive value of mNGS were 95.45, 37.50, 80.77, and 75.00%, respectively. The sensitivity, specificity, positive predictive value, and negative predictive value of the traditional methods were 72.72, 62.50, 84.21, and 45.45%, respectively. The clinical compliance of mNGS was 80.00%, and that of the traditional method was 70.00%. The sensitivity and negative predictive value of mNGS were high, and the difference in the sensitivity for detecting G+ bacteria was statistically significant (p < 0.05). However, the differences in G- bacteria, fungi, and Mycoplasma/Chlamydia were not statistically significant (p > 0.05). Due to the small sample size, statistical analysis could not be conducted on viral
利用元基因组下一代测序(mNGS)分析儿童难治性肺炎的病原体分布。本研究共纳入2019年9月至2021年12月在首都儿科研究所附属儿童医院呼吸内科接受治疗的60例难治性肺炎患儿。收集临床资料(包括性别、年龄、实验室检查、并发症和出院诊断)和下呼吸道标本,包括支气管肺泡灌洗液(BALF)、深部痰液、胸腔积液、肺脓肿穿刺液、传统呼吸道病原体(培养、酸-ast 染色、聚合酶链反应、血清学检测等)和 mNGS 检测方法。)和 mNGS 检测方法来确定难治性肺炎患儿的病原体分布情况,并比较 mNGS 和传统病原体检测方法对不同类型病原体的阳性率和诊断效率。在 60 名难治性肺炎患儿中,43 份标本经 mNGS 检测呈阳性,检测出 67 株病原体,其中肺炎支原体占 20.90%(14 株),肺炎链球菌占 11.94%(8 株),巨细胞病毒占 7.46%(5 株),白色念珠菌占 5.97%(4 株)。使用传统方法检测到 39 株肺炎支原体(41.03%,16 株)、肺炎链球菌(10.26%,4 株)、白色念珠菌(7.69%,3 株)和曲霉菌(5.13%,2 株)。mNGS 检测的阳性率为 90.48%,传统方法的阳性率为 61.90%(p = 0.050),尤其是 G+ 细菌。mNGS 的阳性率高于传统方法(P 0.05)。在儿童难治性肺炎的病原学诊断中,mNGS 的总体疗效高于传统方法。应用 mNGS 可显著提高难治性肺炎患儿的病原体检出率。mNGS 检测 G+ 细菌的灵敏度和阴性预测值均高于其他方法,并能排除原有的可疑致病菌。减少了不必要的抗生素使用,但在 G- 细菌、真菌或支原体/衣原体方面没有显著的统计学差异。
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引用次数: 0
Gut microbiota, plasma metabolites, and osteoporosis: unraveling links via Mendelian randomization 肠道微生物群、血浆代谢物与骨质疏松症:通过孟德尔随机化揭示联系
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1433892
Yi Lu, Xiaobing Cai, Baohua Shi, Haitao Gong
Osteoporosis, characterized by reduced bone density and heightened fracture risk, is influenced by genetic and environmental factors. This study investigates the interplay between gut microbiota, plasma metabolomics, and osteoporosis, identifying potential causal relationships mediated by plasma metabolites.Utilizing aggregated genome-wide association studies (GWAS) data, a comprehensive two-sample Mendelian Randomization (MR) analysis was performed involving 196 gut microbiota taxa, 1,400 plasma metabolites, and osteoporosis indicators. Causal relationships between gut microbiota, plasma metabolites, and osteoporosis were explored.The MR analyses revealed ten gut microbiota taxa associated with osteoporosis, with five taxa positively linked to increased risk and five negatively associated. Additionally, 96 plasma metabolites exhibited potential causal relationships with osteoporosis, with 49 showing positive associations and 47 displaying negative associations. Mediation analyses identified six causal pathways connecting gut microbiota to osteoporosis through ten mediating relationships involving seven distinct plasma metabolites, two of which demonstrated suppression effects.This study provides suggestive evidence of genetic correlations and causal links between gut microbiota, plasma metabolites, and osteoporosis. The findings underscore the complex, multifactorial nature of osteoporosis and suggest the potential of gut microbiota and plasma metabolite profiles as biomarkers or therapeutic targets in the management of osteoporosis.
骨质疏松症以骨密度降低和骨折风险增加为特征,受遗传和环境因素的影响。这项研究调查了肠道微生物群、血浆代谢组学和骨质疏松症之间的相互作用,确定了由血浆代谢物介导的潜在因果关系。利用全基因组关联研究(GWAS)的汇总数据,进行了一项全面的双样本孟德尔随机化(MR)分析,涉及 196 个肠道微生物群分类群、1,400 种血浆代谢物和骨质疏松症指标。MR分析显示,10个肠道微生物群分类群与骨质疏松症有关,其中5个分类群与风险增加呈正相关,5个呈负相关。此外,96 种血浆代谢物与骨质疏松症有潜在的因果关系,其中 49 种呈正相关,47 种呈负相关。这项研究提供了肠道微生物群、血浆代谢物和骨质疏松症之间遗传相关性和因果联系的提示性证据。这些发现强调了骨质疏松症的复杂性和多因素性,并表明肠道微生物群和血浆代谢物谱有可能成为治疗骨质疏松症的生物标志物或治疗目标。
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引用次数: 0
Generating open-source 3D phytoplankton models by integrating photogrammetry with scanning electron microscopy 将摄影测量与扫描电子显微镜相结合,生成开源三维浮游植物模型
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1429179
Xuerong Sun, Robert J. W. Brewin, Christian Hacker, Johannes J. Viljoen, Mengyu Li
The community structure and ecological function of marine ecosystems are critically dependent on phytoplankton. However, our understanding of phytoplankton is limited due to the lack of detailed information on their morphology. To address this gap, we developed a framework that combines scanning electron microscopy (SEM) with photogrammetry to create realistic 3D (three-dimensional) models of phytoplankton. The workflow of this framework is demonstrated using two marine algal species, one dinoflagellate Prorocentrum micans and one diatom Halamphora sp. The resulting 3D models are made openly available and allow users to interact with phytoplankton and their complex structures virtually (digitally) and tangibly (3D printing). They also allow for surface area and biovolume calculations of phytoplankton, as well as the exploration of their light scattering properties, which are both important for ecosystem modeling. Additionally, by presenting these models to the public, it bridges the gap between scientific inquiry and education, promoting broader awareness on the importance of phytoplankton.
海洋生态系统的群落结构和生态功能严重依赖浮游植物。然而,由于缺乏浮游植物形态的详细信息,我们对浮游植物的了解十分有限。为了弥补这一不足,我们开发了一个框架,将扫描电子显微镜(SEM)与摄影测量相结合,创建逼真的浮游植物三维(三维)模型。我们使用两种海洋藻类(一种是甲藻 Prorocentrum micans,另一种是硅藻 Halamphora sp.)演示了这一框架的工作流程。所生成的三维模型可公开使用,用户可以虚拟(数字)和实际(三维打印)地与浮游植物及其复杂结构进行交互。用户还可以利用这些模型计算浮游植物的表面积和生物体积,并探索其光散射特性,这对于生态系统建模非常重要。此外,通过向公众展示这些模型,它还在科学探索和教育之间架起了一座桥梁,促进人们更广泛地认识浮游植物的重要性。
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引用次数: 0
Combined analysis of the microbiome and metabolome to reveal the characteristics of saliva from different diets: a comparison among vegans, seafood-based omnivores, and red meat (beef and lamb) omnivores 综合分析微生物组和代谢组,揭示不同饮食习惯的唾液特征:素食者、海鲜杂食者和红肉(牛肉和羊肉)杂食者之间的比较
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1419686
Shiyu Sun, Huiqiong Zhang, Linying Ye, Litao Huang, Jieyu Du, Xiaomin Liang, Xiaofeng Zhang, Jiaxing Chen, Yingping Jiang, Ling Chen
Revealing individual characteristics is supportive for identifying individuals in forensic crime. As saliva is one of the most common biological samples used in crime scenes, it is important to make full use of the rich individual information contained in saliva. The aim of this study was to explore the application of the microbiome in forensic science by analysing differences in the salivary microbiome and metabolome of healthy individuals with different dietary habits.We performed 16S rDNA sequencing analysis based on oral saliva samples collected from 12 vegetarians, 12 seafood omnivores and 12 beef and lamb omnivores. Non-targeted metabolomics analyses were also performed based on saliva samples from healthy individuals.The results showed that the dominant flora of vegetarians was dominated by Neisseria (belonging to the phylum Proteobacteria), while seafood omnivores and beef and lamb omnivores were dominated by Streptococcus (belonging to the phylum Firmicutes). NDMS-based and cluster analyses showed that vegetarian dieters were significantly differentiated from meat dieters (seafood omnivores and beef and lamb omnivores), which may be related to the fact that high-fiber diets can create a different salivary flora structure. Variants were also detected in salivary metabolic pathways, including positive correlations with Lipid metabolism, Amino acid metabolism, Carbohydrate metabolism, and Nucleotide metabolism in vegetarians, and correlations in seafood omnivores. In order to select salivary microorganisms and metabolic markers that can distinguish different dietary profiles, a random forest classifier model was constructed in this study, and the results showed that individuals with different dietary profiles could be successfully distinguished based on the core genera and metabolites such as Streptococcus, Histidinyl-Valine.Our study provides a supportive basis for the application of salivary polyomics in order to reveal the dietary characteristics of individuals for forensic investigation and crime solving.
揭示个体特征有助于鉴别法医犯罪中的个体。由于唾液是犯罪现场最常用的生物样本之一,因此充分利用唾液中蕴含的丰富个体信息非常重要。本研究旨在通过分析不同饮食习惯的健康人唾液微生物组和代谢组的差异,探索微生物组在法医学中的应用。我们根据从 12 名素食者、12 名海鲜杂食者和 12 名牛羊肉杂食者采集的口腔唾液样本进行了 16S rDNA 测序分析。结果显示,素食者的优势菌群主要是奈瑟氏菌(属于变形菌门),而海鲜杂食者和牛羊肉杂食者的优势菌群主要是链球菌(属于真菌门)。基于 NDMS 和聚类的分析表明,素食者与肉食者(海鲜杂食者和牛羊肉杂食者)有显著差异,这可能与高纤维饮食会产生不同的唾液菌群结构有关。在唾液代谢途径中也发现了变异,包括与素食者的脂质代谢、氨基酸代谢、碳水化合物代谢和核苷酸代谢呈正相关,以及与海鲜杂食者的相关。为了选择能够区分不同饮食特征的唾液微生物和代谢标记物,本研究构建了一个随机森林分类器模型,结果表明,根据链球菌、组苷缬氨酸等核心菌属和代谢产物,可以成功区分不同饮食特征的个体。
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引用次数: 0
Comparative evaluation of 16S rRNA primer pairs in identifying nitrifying guilds in soils under long-term organic fertilization and water management 比较评估 16S rRNA 引物对识别长期有机施肥和水管理条件下土壤硝化区系的作用
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1424795
Xue Zhou, Xiaoyin Liu, Meiyu Liu, Weixuan Liu, Junzeng Xu, Yawei Li
Compared with 454 sequencing technology, short-read sequencing (e.g., Illumina) technology generates sequences of high accuracy, but limited length (<500 bp). Such a limitation can prove that studying a target gene using a large amplicon (>500 bp) is challenging. The ammonia monooxygenase subunit A (amoA) gene of ammonia-oxidizing archaea (AOA), which plays a crucial part in the nitrification process, is such a gene. By providing a full overview of the community of a functional microbial guild, 16S ribosomal ribonucleic acid (rRNA) gene sequencing could overcome this problem. However, it remains unclear how 16S rRNA primer selection influences the quantification of relative abundance and the identification of community composition of nitrifiers, especially AOA. In the present study, a comparison was made between the performance of primer pairs 338F-806R, 515F-806R, and 515F-907R to a shotgun metagenome approach. The structure of nitrifier communities subjected to different long-term organic matter amendment and water management protocols was assessed. Overall, we observed higher Chao1 richness diversity of soil total bacteria by using 515F-806R compared to 338F-806R and 515F-907R, while higher Pielou’s evenness diversity was observed by using 515F-806R and 515F-907R compared to 338F-806R. The studied primer pairs revealed different performances on the relative abundance of Thaumarchaeota, AOB, and NOB. The Thaumarchaeota 16S rRNA sequence was rarely detected using 338F-806R, while the relative abundances of Thaumarchaeota detected using 515F-806R were higher than those detected by using 515F-907R. AOB showed higher proportions in the 338F-806R and 515F-907R data, than in 515F-806R data. Different primers pairs showed significant change in relative proportion of NOB. Nonetheless, we found consistent patterns of the phylotype distribution of nitrifiers in different treatments. Nitrosopumilales (NP) and Nitrososphaerales (NS) clades were the dominant members of the AOA community in soils subject to controlled irrigation, whereas Ca. Nitrosotaleales (NT) and NS clades dominated the AOA community in soils subject to flooding irrigation. Nitrospira lineage II was the dominant NOB phylotype in all samples. Overall, ideal 16S rRNA primer pairs were identified for the analysis of nitrifier communities. Moreover, NP and NT clades of AOA might have distinct environmental adaptation strategies under different irrigation treatments.
与 454 测序技术相比,短线程测序(如 Illumina)技术产生的序列精度高,但长度有限(500 bp),具有挑战性。在硝化过程中起关键作用的氨氧化古细菌(AOA)的氨单加氧酶亚基 A(amoA)基因就是这样的基因。16S 核糖体核糖核酸(rRNA)基因测序可提供功能微生物群落的全貌,从而克服这一问题。然而,16S rRNA 引物选择如何影响硝化细菌(尤其是 AOA)相对丰度的量化和群落组成的鉴定,目前仍不清楚。本研究比较了 338F-806R、515F-806R 和 515F-907R 引物对霰弹枪元基因组方法的性能。我们对硝化细菌群落的结构进行了评估,这些群落受到了不同的长期有机物添加和水管理方案的影响。总体而言,与 338F-806R 和 515F-907R 相比,我们观察到使用 515F-806R 的土壤细菌总数具有更高的 Chao1 丰富度多样性,而与 338F-806R 相比,使用 515F-806R 和 515F-907R 的土壤细菌总数具有更高的 Pielou 均匀度多样性。所研究的引物对揭示了潮虫、AOB 和 NOB 相对丰度的不同表现。使用 338F-806R 很少能检测到 Thaumarchaeota 16S rRNA 序列,而使用 515F-806R 检测到的 Thaumarchaeota 相对丰度高于使用 515F-907R 检测到的相对丰度。338F-806R 和 515F-907R 数据中 AOB 的比例高于 515F-806R 数据。不同引物对中 NOB 的相对比例有显著变化。不过,我们发现不同处理中硝化细菌的系统型分布模式是一致的。在控制灌溉的土壤中,亚硝化藻类(NP)和亚硝化藻类(NS)支系是 AOA 群落的主要成员,而 Ca.而在大水漫灌的土壤中,亚硝基藻类(NT)和 NS 支系在 AOA 群落中占主导地位。在所有样本中,硝化螺菌 II 系是主要的 NOB 系统型。总体而言,为硝化细菌群落分析确定了理想的 16S rRNA 引物对。此外,在不同的灌溉处理下,AOA 的 NP 和 NT 支系可能具有不同的环境适应策略。
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引用次数: 0
Towards sustainable biocontrol: inhibition of soil borne fungi by microalgae from harsh environments 实现可持续生物控制:恶劣环境中的微藻对土壤真菌的抑制作用
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1433765
Dikla Eckstien, Noga Maximov, Nofet Margolis, Hagai Raanan
Using microorganisms as biocontrol agents against soilborne plant pathogens is a promising alternative to chemical pesticides. However, only some biocontrol agents have proven effective under field conditions. This study explores the potential of highly resilient microalgae isolated from harsh environments, such as Biological Soil Crusts and agricultural fields in semi-arid regions, as a novel and sustainable approach to biocontrol. Fifty-nine microalgal strains, including thirteen cyanobacteria and forty-six green algae, were isolated and identified. Dual-culture plate assays and toxicity tests of microalgal growth media were conducted to evaluate the antifungal activity of the isolates against eight representative soilborne pathogens. The results showed that many microalgae strains exhibited significant inhibitory effects on the growth of specific fungal pathogens, although the activity varied among different microalgal strains and pathogen species. Some strains even promoted the growth of certain fungi. The lack of a clear pattern in the antifungal activity highlights the complexity and specificity of the interactions between microalgae and soilborne pathogens. An “Inhibition Effectiveness” metric was developed to quantify biocontrol potential based on fungal growth inhibition. The green algal genus Desmodesmus, particularly Desmodesmus subspicatus isolates, showed higher antifungal efficacy than other genera. While the inhibitory mechanisms remain unclear, the results demonstrate the promising biocontrol capabilities of microalgae from extreme environments like BSCs. Further research could unlock novel opportunities for sustainable disease management by harnessing specific microalgal strains or synergistic strain combinations targeting soilborne pathogens.
利用微生物作为生物控制剂来防治土壤中的植物病原体,是替代化学农药的一种很有前途的方法。然而,只有一些生物控制剂在田间条件下被证明是有效的。本研究探索了从半干旱地区的生物土壤结壳和农田等恶劣环境中分离出来的高弹性微藻作为一种新型和可持续的生物控制方法的潜力。研究人员分离并鉴定了 59 株微藻类,包括 13 株蓝藻和 46 株绿藻。对微藻生长培养基进行了双培养平板试验和毒性试验,以评估分离菌株对八种代表性土传病原体的抗真菌活性。结果表明,许多微藻菌株对特定真菌病原体的生长具有显著的抑制作用,但不同微藻菌株和病原体种类之间的活性存在差异。有些菌株甚至能促进某些真菌的生长。抗真菌活性缺乏明确的模式,这凸显了微藻与土传病原体之间相互作用的复杂性和特异性。根据对真菌生长的抑制作用,开发了一种 "抑制效果 "指标来量化生物防治潜力。绿藻属 Desmodesmus,特别是 Desmodesmus subspicatus 分离物的抗真菌效力高于其他属。虽然抑制机制尚不清楚,但研究结果表明,来自 BSCs 等极端环境的微藻具有良好的生物控制能力。通过利用特定的微藻菌株或针对土传病原体的协同菌株组合,进一步的研究可以为可持续病害管理提供新的机遇。
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引用次数: 0
Rapid identification of bloodstream infection pathogens and drug resistance using Raman spectroscopy enhanced by convolutional neural networks 利用卷积神经网络增强的拉曼光谱技术快速识别血流感染病原体和耐药性
Pub Date : 2024-07-15 DOI: 10.3389/fmicb.2024.1428304
Haiquan Kang, Ziling Wang, Jingfang Sun, Shuang Song, Lei Cheng, Yi Sun, Xingqi Pan, Changyu Wu, Ping Gong, Hongchun Li
Bloodstream infections (BSIs) are a critical medical concern, characterized by elevated morbidity, mortality, extended hospital stays, substantial healthcare costs, and diagnostic challenges. The clinical outcomes for patients with BSI can be markedly improved through the prompt identification of the causative pathogens and their susceptibility to antibiotics and antimicrobial agents. Traditional BSI diagnosis via blood culture is often hindered by its lengthy incubation period and its limitations in detecting pathogenic bacteria and their resistance profiles. Surface-enhanced Raman scattering (SERS) has recently gained prominence as a rapid and effective technique for identifying pathogenic bacteria and assessing drug resistance. This method offers molecular fingerprinting with benefits such as rapidity, sensitivity, and non-destructiveness. The objective of this study was to integrate deep learning (DL) with SERS for the rapid identification of common pathogens and their resistance to drugs in BSIs. To assess the feasibility of combining DL with SERS for direct detection, erythrocyte lysis and differential centrifugation were employed to isolate bacteria from blood samples with positive blood cultures. A total of 12,046 and 11,968 SERS spectra were collected from the two methods using Raman spectroscopy and subsequently analyzed using DL algorithms. The findings reveal that convolutional neural networks (CNNs) exhibit considerable potential in identifying prevalent pathogens and their drug-resistant strains. The differential centrifugation technique outperformed erythrocyte lysis in bacterial isolation from blood, achieving a detection accuracy of 98.68% for pathogenic bacteria and an impressive 99.85% accuracy in identifying carbapenem-resistant Klebsiella pneumoniae. In summary, this research successfully developed an innovative approach by combining DL with SERS for the swift identification of pathogenic bacteria and their drug resistance in BSIs. This novel method holds the promise of significantly improving patient prognoses and optimizing healthcare efficiency. Its potential impact could be profound, potentially transforming the diagnostic and therapeutic landscape of BSIs.
血流感染(BSI)是一个重要的医学问题,其特点是发病率和死亡率升高、住院时间延长、医疗成本高昂以及诊断困难。通过及时识别致病病原体及其对抗生素和抗菌药的敏感性,可以显著改善 BSI 患者的临床治疗效果。传统的 BSI 诊断方法是通过血液培养,但由于培养潜伏期较长,而且在检测病原菌及其耐药性方面存在局限性,因此往往难以达到诊断目的。最近,表面增强拉曼散射(SERS)作为一种快速、有效的鉴定病原菌和评估耐药性的技术而备受瞩目。这种方法具有快速、灵敏和非破坏性等优点,可进行分子指纹识别。本研究的目的是将深度学习(DL)与 SERS 相结合,用于快速鉴定 BSI 中的常见病原体及其耐药性。为了评估将深度学习与 SERS 结合用于直接检测的可行性,研究人员采用了红细胞裂解和差速离心法,从血液培养阳性的血液样本中分离细菌。使用拉曼光谱从这两种方法中分别收集了 12,046 和 11,968 个 SERS 光谱,随后使用 DL 算法进行了分析。研究结果表明,卷积神经网络(CNN)在识别流行病原体及其耐药菌株方面具有相当大的潜力。在从血液中分离细菌方面,差速离心技术优于红细胞裂解技术,对病原菌的检测准确率达 98.68%,在识别耐碳青霉烯类肺炎克雷伯菌方面的准确率高达 99.85%,令人印象深刻。总之,这项研究成功地开发了一种创新方法,将 DL 与 SERS 相结合,用于快速鉴定 BSIs 中的病原菌及其耐药性。这种新方法有望大大改善患者的预后并优化医疗效率。它的潜在影响可能是深远的,有可能改变 BSIs 的诊断和治疗格局。
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引用次数: 0
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Frontiers in Microbiology
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