Related Experiment Video
Updated: May 20, 2026

Demonstrating a Multi-drug Resistant Mycobacterium tuberculosis Amplification Microarray
Published on: April 25, 2014
Molecular typing and epidemiological investigation of clinical populations of Pseudomonas aeruginosa using an
Annalisa Ballarini1, Giovanna Scalet, Malgorzata Kos
1Centre for Integrative Biology, University of Trento, Trento, Italy. ballarini@science.unitn.it
Background:
Pseudomonas aeruginosa is an opportunistic pathogen which has the potential to become extremely harmful in the nosocomial environment, especially for cystic fibrosis (CF) patients, who are easily affected by chronic lung infections. For epidemiological purposes, discriminating P.aeruginosa isolates is a critical step, to define distribution of clones among hospital departments, to predict occurring microevolution events and to correlate clones to their source. A collection of 182 P. aeruginosa clinical strains isolated within Italian hospitals from patients with chronic infections, i.e. cystic fibrosis (CF) patients, and with acute infections were genotyped. Molecular typing was performed with the ArrayTube (AT) multimarker microarray (Alere Technologies GmbH, Jena, Germany), a cost-effective, time-saving and standardized method, which addresses genes from both the core and accessory P.aeruginosa genome. Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) were employed as reference genotyping techniques to estimate the ArrayTube resolution power.
Results:
41 AT-genotypes were identified within our collection, among which 14 were novel and 27 had been previously described in publicly available AT-databases. Almost 30% of the genotypes belonged to a main cluster of clones. 4B9A, EC2A, 3C2A were mostly associated to CF-patients whereas F469, 2C1A, 6C22 to non CF. An investigation on co-infections events revealed that almost 40% of CF patients were colonized by more than one genotype, whereas less than 4% were observed in non CF patients. The presence of the exoU gene correlated with non-CF patients within the intensive care unit (ICU) whereas the pKLC102-like island appeared to be prevalent in the CF centre. The congruence between the ArrayTube typing and PFGE or MLST was 0.077 and 0.559 (Adjusted Rand coefficient), respectively.AT typing of this Italian collection could be easily integrated with the global P. aeruginosa AT-typed population, uncovering that most AT-genotypes identified (> 80%) belonged to two large clonal clusters, and included 12 among the most abundant clones of the global population.
Conclusions:
The ArrayTube (AT) multimarker array represented a robust and portable alternative to reference techniques for performing P. aeruginosa molecular typing, and allowed us to draw conclusions especially suitable for epidemiologists on an Italian clinical collection from chronic and acute infections.
Insights
The ArrayTube (AT) multimarker array effectively distinguishes Pseudomonas aeruginosa strains from Italian hospitals. This method is a robust alternative for molecular typing, aiding epidemiological studies in cystic fibrosis (CF) and acute infections.
Area of Science:
- Microbiology
- Genetics
- Epidemiology
Background:
- Pseudomonas aeruginosa is a significant opportunistic pathogen, particularly in nosocomial settings and for cystic fibrosis (CF) patients.
- Effective discrimination of P. aeruginosa isolates is crucial for epidemiological surveillance, tracking clonal distribution, predicting microevolution, and correlating clones with infection sources.
- A collection of 182 P. aeruginosa clinical strains from Italian hospitals, including those from CF patients with chronic infections and patients with acute infections, were genotyped.
Purpose of the Study:
- To evaluate the ArrayTube (AT) multimarker microarray as a cost-effective, time-saving, and standardized method for P. aeruginosa molecular typing.
- To compare the resolution power of AT typing with reference techniques like pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST).
- To analyze the clonal structure and population dynamics of P. aeruginosa strains from Italian clinical settings.
Main Methods:
- Molecular typing of 182 P. aeruginosa clinical strains using the ArrayTube (AT) multimarker microarray.
- Genotyping addressed genes from both the core and accessory P. aeruginosa genome.
- Comparison with reference genotyping techniques: Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST).
Main Results:
- 41 AT-genotypes were identified, with 14 novel and 27 previously described. Approximately 30% of genotypes belonged to a major clone cluster.
- Specific genotypes were associated with CF patients (e.g., 4B9A, EC2A, 3C2A) versus non-CF patients (e.g., F469, 2C1A, 6C22).
- CF patients exhibited higher rates of co-infection (nearly 40%) with multiple genotypes compared to non-CF patients (<4%). The exoU gene correlated with non-CF patients in ICUs, while the pKLC102-like island was prevalent in CF centers. AT typing showed good congruence with MLST (Adjusted Rand coefficient=0.559).
Conclusions:
- The ArrayTube (AT) multimarker array is a robust and portable alternative to reference methods for P. aeruginosa molecular typing.
- AT typing provides valuable epidemiological insights into Italian clinical collections of P. aeruginosa strains from both chronic and acute infections.
- Integration with global AT-typed P. aeruginosa populations revealed that most identified AT-genotypes belonged to two large clonal clusters, including globally abundant clones.
More Related Videos
Related Concept Videos
Modern Molecular Taxonomy
Applications of Molecular Taxonomy
DNA Microarrays
Gene Regulation in Microbial Communities: Quorum Sensing

