MiPortal

Our History

2024
AMGC grant supported the successful in-house production of a component prototype
Microbio successfully completed a project to establish sovereign manufacture of raw materials for a security sensitive biological agent, supported by a grant from Advanced Manufacturing Growth Centre (AMGC).

In-house manufacturing conducted

Microbio conducted full in-house manufacturing of InfectID™-BSI in the Translational Research Institute facilities.

2023
Study results published
Microbio’s preclinical study results were published in the Journal of Microbiological Methods. (Simms, L.A., Davies, C., Jayasundara, N., Sandhu, S., Pintara, A., Pretorius, A., Nimmo, G.R., Harper, J., Hiskens, M., Smith, K., Boxall, S., Lord, A., Giardino, R., Farlow, D., Ward, D.M., Huygens, F., 2023. Performance evaluation of InfectID™-BSI: A rapid quantitative PCR assay for detecting sepsis-associated organisms directly from whole blood. Journal of Microbiological Methods 211, 106783.)
2022
Microbio receives ISO 13485:2016 certification
Following an audit by British Standards Institution (BSI Group), Microbio was granted ISO 13485:2016 certification for its Quality Management System.

InfectID™-BSI tests approved for sale in Europe and UK

Microbio’s flagship sepsis test, designed to identify 26 common sepsis-causing pathogens in less than 3 hours received clearance for sale in Europe under IVD Directive 98/79/EC

2021
InfectID™-COVID-19 tests approved for sale in Europe

Microbio developed two SARS-CoV-2 tests and received approval for sale in Europe under IVD Directive 98/79/EC

InfectID™-COVID-19-Replication identifies the presence of replication-competent (the ‘live’, multiplying) SARS-CoV-2 virus

InfectID™-COVID-19-Detection identifies the presence of the SARS-CoV-2 virus, including the active virus and inactive particles being shed by the body.

2020
Commercialisation potential acknowledged with Accelerating Commercialisation Grant

In late 2020, Microbio was awarded a Federal Government Accelerating Commercialisation Grant to commercialise InfectID™-Blood Stream Infection (BSI) diagnostic assay.

Series A capital raise supports expansion of team

A Series A capital raise closed on 30 September 2020. This funding allowed for the continued growth of the team to facilitate the commercialisation of InfectID™. The emergence of COVID-19 motivated the team to develop a SARS-CoV-2 test designed to identify the presence of replicating virus.

2019
Seed funding raised to conduct preclinical verification
An initial funding round provided the capital to establish the laboratory research team.

InfectID™-BSI prototype tested in a successful patient study

Preclinical testing conducted on patient whole blood samples from 203 patients from two Queensland Hospitals.

2017
Microbio founded to take InfectID™ to market
Microbio was founded in 2017 by Dr Huygens and Paul Carboon. Their aim was to build a scientific and commercialisation team to bring Microbio’s pathogen diagnostic test out of the laboratory and into the market to benefit human health and wellbeing.
2015
Clinical research demonstrates the approach’s specificity
In 2015, Dr Huygens led a collaborative trial with the Microbiology Central Laboratory, Pathology Queensland, which involved testing 300 patient samples: 100 negative samples and 200 positive samples. The study found that InfectID™ had a specificity of 98.5% in correctly identifying bacterial species from blood samples.
2004
A novel pathogen identification approach using DNA ‘fingerprints’

Dr Flavia Huygens developed and validated a process that identifies pathogens by targeting Single Nucleotide Polymorphisms (SNPs), a pathogen’s DNA ‘fingerprint’, found at a specific point in its genetic code. By focusing on SNPs rather than the whole genome, the process is fast, inexpensive, highly sensitive and can be adapted to address different target pathogens.

This technology was considered a world-first and is unique in its design and application, leading to several publications.

The test was refined and became InfectID™, which uses real-time PCR followed by high-resolution melt-curve analysis to identify pathogen species directly from whole blood without the need to pre-culture.