Related Experiment Video
Updated: Jan 21, 2026

07:17
Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues
Published on: August 23, 2024
1.8K
Multilocus Sequence Typing (MLST) of Chlamydiales
Martina Jelocnik1, Adam Polkinghorne2, Yvonne Pannekoek3
1Genecology Research Centre, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
Methods in Molecular Biology (Clifton, N.J.)
|August 7, 2019
Summary
Multilocus Sequence Typing (MLST) provides a universal molecular barcode for bacterial and eukaryotic organisms. This study details MLST methods for analyzing Chlamydiales bacteria, using a specific scheme for Chlamydia pecorum.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Multilocus Sequence Typing (MLST) is a widely adopted molecular method for bacterial and eukaryotic organism characterization.
- MLST relies on sequencing conserved housekeeping (HK) genes to generate allelic profiles, forming a unique sequence type (ST) or 'molecular barcode'.
Purpose of the Study:
- To describe the principles and molecular approaches for generating MLST data.
- To demonstrate the application of MLST for analyzing bacteria within the order Chlamydiales.
- To present a specific MLST scheme developed for Chlamydia pecorum.
Main Methods:
- Utilized DNA sequencing of conserved housekeeping genes.
- Assigned allelic numbers to gene sequences.
- Combined allelic profiles to define sequence types (STs).
Main Results:
- Established a Chlamydia pecorum-specific MLST scheme.
- Demonstrated the generation of MLST data for Chlamydiales analysis.
Conclusions:
- MLST is a powerful and versatile tool for fine-detailed molecular typing of diverse organisms.
- The described Chlamydia pecorum MLST scheme facilitates robust analysis within the Chlamydiales order.
Related Concept Videos
Types of RNA
72.6K
Overview
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA...
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA...
72.6K
Cis-regulatory Sequences
11.6K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
11.6K
Sanger Sequencing
773.5K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
773.5K
Types of Hormones
83.1K
Hormones can be classified into three main types based on their chemical structures: steroids, peptides, and amines. Their actions are mediated by the specific receptors they bind to on target cells.
83.1K
Next-generation Sequencing
97.9K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
97.9K
Maxam-Gilbert Sequencing
12.7K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
12.7K

