Our comprehensive microbial identification platform, encompassing methodologies such as Rep-PCR, MicroSEQ®, NGS-based microbial identification, multi-locus sequence typing, and mycoplasma detection, is designed to identify microbial species with efficiency and cost-effectiveness. This system supports high-throughput and streamlined processes to deliver data with exceptional accuracy and sensitivity, thereby advancing your microbial and laboratory research objectives.
Microbiological identification entails a spectrum of methodologies aimed at discerning the identity of microorganisms by examining their distinct physical, biochemical, and genetic profiles. These minute entities, despite their microscopic dimensions, serve pivotal roles in ecosystems by significantly contributing to the biodiversity of various environments such as soil, water, and air. Moreover, microorganisms profoundly influence human health; they participate in beneficial processes including digestion and immune regulation, while also being implicated in infections and diseases.
The process of microbial identification is instrumental in elucidating microbial diversity, identifying pathogenic organisms, and assessing treatment efficacy in clinical settings. Methodologies for identification predominantly fall into two categories: phenotypic identification, which emphasizes observable characteristics such as morphology and biochemical reactions, and genotypic identification, which utilizes molecular techniques to analyze genetic material, offering enhanced precision.
Phenotypic identification involves methods that characterize microorganisms based on observable traits and biochemical properties. This includes techniques such as the API and VITEK systems, MALDI-TOF MS, and the Biolog system.
The API and VITEK systems are automated platforms that classify microorganisms by assessing their biochemical and physiological characteristics, streamlining the identification process through comparison with comprehensive databases; however, their accuracy may be compromised by the quality of these databases, particularly for certain species like Bacillus and cocci. Similarly, MALDI-TOF MS employs mass spectrometry to quickly and accurately analyze microbial protein profiles, making it ideal for high-throughput environments, though it depends on a robust database for reliable results, necessitating additional methods for ambiguous identifications. The Biolog system evaluates microbial metabolic activity based on their ability to utilize various carbon sources, providing a user-friendly interface and extensive metabolic profiles, but its effectiveness also hinges on the quality of the underlying database.
Genotypic identification methods utilize genetic information to accurately classify microorganisms, providing insights beyond observable traits. Key techniques in this category include Whole Genome Sequencing (WGS), 16S rRNA sequencing, genetic fingerprinting, and additional molecular techniques.
Whole Genome Sequencing (WGS) provides detailed insights into the genetic composition of microorganisms, facilitating accurate identification and traceability; however, it is more costly and resource-intensive than alternative methods. In contrast, 16S rRNA sequencing targets the conserved 16S rRNA gene found in all bacteria, enabling species identification based on genetic sequences, though it may lack resolution when differentiating closely related species. Genetic fingerprinting utilizes restriction enzymes to fragment microbial DNA, creating unique patterns for comparison with reference databases, yet it can struggle to distinguish closely related strains. Additionally, other genotypic methods, including quantitative PCR (qPCR), gene chips, and PFGE/DGGE, offer further identification options: qPCR quantifies specific DNA sequences, gene chips detect multiple genetic markers simultaneously, and PFGE/DGGE facilitate strain-level analysis through size or sequence variation.
The identification of microorganisms is critical for quality control, contamination detection, root cause analysis, and various microbiological studies. Consequently, microbial identification is extensively employed across diverse sectors, including agricultural production, environmental protection, research laboratories, academic institutions, biotechnology, and the pharmaceutical industry. Moreover, the precise identification of microbial pathogens is indispensable for understanding and managing numerous infectious disease syndromes.
We offer microbial identification using various methods and platforms. Our specific services are as follows:
Based on the samples you submit and your objectives, we will select the most suitable microbial identification method for your project to achieve high-throughput and accurate microbial identification.
Note: The above content includes only a portion of the bioinformatics analysis. For more information or to customize the analysis, please contact us directly.
Our bioinformatics analyses include these parts: routine identification analysis, composition analysis, diversity analysis, comparative analysis, evolutionary analysis. We are flexible to your specific needs.
Bioinformatics analysis | Details | |
---|---|---|
Routine identification analysis | Morphological characteristics and physical and chemical properties of the sample | |
Composition analysis | Rank-abundance curve | Determine the abundance and evenness of the species in the sample |
OUT classification | Identify species and genera | |
Diversity analysis | Alpha diversity | The diversity of communities within a particular area or ecosystem |
Beta-analysis | Comparative studies of abundant features between samples | |
Comparative analysis | PCA | Study the relationships between microbial populations |
NMDS analysis | Reveal how similar/dissimilar certain samples are or how the microbial composition is changing over time | |
LDA | Show clear clustering by microbial composition between the study groups | |
Evolutionary analysis | Construction of phylogenetic tree |
Note: If you wish to obtain more accurate and detailed information regarding sample requirements, please feel free to contact us directly.
Partial results of our Microbial Identification service are shown below:
Please feel free to reach out if you have any further inquiries or require additional information.
Transferrable protection by gut microbes against STING-associated lung disease
Journal: Cell Reports
Impact factor: 8.8
Published: 11 May 2021
Backgrounds
The STING pathway regulates immune responses to pathogens and is linked to autoimmune diseases like STING-associated vasculopathy with onset in infancy (SAVI). This study demonstrates that gut anaerobes can mitigate autoinflammatory lung disease in a SAVI mouse model. The researchers used an antibiotic that preserved certain gut bacteria, leading to protection against lung disease, and identified beneficial Bacteroidales species through metagenomic sequencing.
Materials & Methods
Sample preparation:
Results
The presence of Bacteroidales is linked to protection against STING-associated lung disease in mice. Metagenomic and 18S analyses showed no changes in eukaryotic gut microbiota between treated and untreated SAVI mice. Germ-free mice that received microbiota from antibiotic-treated mice had fewer bacterial reads and a predominance of Bacteroidales, such as Muribaculum. These findings indicate that an enrichment of Bacteroidales, alongside a reduction in other gut bacteria, may confer protection against autoinflammatory lung disease.
Fig 1. Bacterial species obtained from metagenomic sequencing.
Conclusion
STING gain-of-function mutations cause lung disease in SAVI mice, which can be mitigated by specific gut bacteria, particularly Bacteroidales that produce short-chain fatty acids. This suggests a potential gut-lung axis influencing autoimmunity and highlights the need for further research into microbial metabolites for therapeutic applications.
Reference
Platt DJ, Lawrence D, Rodgers R, et al. Transferrable protection by gut microbes against STING-associated lung disease. Cell reports. 2021, 35(6).
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