Name: Micro-Colony Forming Unit Assay to Quantify Mycobacteria
Uploaded: 2023-07-28T13:10:00
Description: Watch this Scientific Journal Video about Micro-Colony Forming Unit Assay to Quantify Mycobacteria at JoVE.com

micro-colony forming unit assay to quantify mycobacteria

Aceleración de la determinación de la tuberculosis mediante el método de micro-UFC

Tuberculosis (TB) is the leading cause of death worldwide by a single infectious agent, bacterium Mycobacterium tuberculosis (M.tb), killing more people than any other pathogen. In 2021, TB was responsible for 1.6 million deaths and was surpassed by COVID-19 during the 2019-2021 pandemic1. Moreover, according to the World Health Organization&#180;s global TB report of 2022, the COVID-19 pandemic was responsible for an increase in new TB cases. The WHO also reports large drops in the number of people diagnosed with TB during this period, which could increase further the number of TB cases1.
The Bacillus Calmette-Gu&#233;rin (BCG) is a live-attenuated strain of the pathogenic Mycobacterium bovis, used for the first time as a vaccine more than 100 years ago. This is the only vaccine against TB and is the oldest licensed vaccine in the world still in use2,3. Currently, there are 12 vaccines in different phases of clinical trials4, and dozens of vaccines are under pre-clinical development5,6. Pre-clinical assessment of vaccines against TB includes the evaluation of the safety and immunogenicity7, which can be obtained in diverse animal models such as zebrafish, mice, guinea pigs, rabbits, cattle, and non-human primates8,9,10. Additionally, assessing the capacity of a vaccine to induce protection against M.tb infection and/or transmission, i.e., the vaccine efficacy, requires an M.tb challenge in vivo5,11. Interestingly, BCG vaccination induces non-specific effects that affect the survival of other bacterial and viral pathogens12,13&#160;through the mechanism of trained immunity14. To quantify the viable bacterial burden in an infected animal, the method of choice is the enumeration of bacterial colonies through the colony-forming units (CFU) assay5,15. CFU is a unit that estimates the number of microorganisms (bacteria or fungi) that form colonies under specific growth conditions. CFUs originate from viable and replicative microorganisms, and the absolute number of living microorganisms within each colony is difficult to estimate. It is uncertain whether a colony has originated from one or more microorganisms. The CFU unit reflects this uncertainty, hence a great variability can be observed in replicates of the same sample. This time-consuming assay requires specialized technicians trained to work in a biosafety level 3 (BSL3) facility, substantial laboratory and incubator space, takes from 4 to 6 weeks to conclude, and is prone to contamination.
In this study, we describe an optimized method for colony enumeration, the micro-CFU (mCFU), and offer a simple and rapid solution to analyze the results15,16,17,18,19,20. The mCFU assay requires tenfold fewer reagents, reduces the incubation period threefold, taking 1 to 2 weeks to conclude, reduces lab space and reagent cost, and minimizes the health and safety risks associated with working with large numbers of M.tb. We propose that this method should be universally adopted for pre-clinical studies of vaccine efficacy determination, ultimately leading to time reduction in the development of vaccines against TB. Finally, this optimized method of CFU enumeration has been used to quantify not only Mycobacteria but also other bacteria, such as Escherichia coli and Ralstonia solanacearum21.

Autor destacado: Optimización de la determinación de UFC para una evaluación eficiente de la eficacia de la vacuna contra la tuberculosis y el análisis de la presentación de antígenos 

Ensayo de la unidad formadora de microcolonias para la evaluación de la eficacia de las vacunas contra la tuberculosis

CFU determination is necessary to measure the efficacy of the immune response against bacteria. However, it is very low throughput and becomes cumbersome and expensive when applied to pathogenic bacteria such as Mycobacterium tuberculosis. This is a significant limitation when we need to test large panels of treatments.The research focuses on tuberculosis and on the assessments of TB vaccines. It explores safety, immunogenicity, and efficacy of vaccines against Mycobacterium tuberculosis. The study presents an optimized method to micro-CFU for enumerating bacterial colonies to assess vaccine efficacy in preclinical studies.This protocol aims to optimize CFU determination by generating results from a small droplet similar to those from a regular Petri dish. Quantifying bacteria viability from such a small sample allows us to analyze thousands of data points using a fraction of the materials and time necessary for the classical method. Our research aims to dissect the antigen presentation machinery and to identify the most relevant antigens to optimize antigen presentation.This will inform us to design and develop better vaccines to improve or replace the current TB vaccine, which is BCG.

Watch this Scientific Journal Video about Micro-Colony Forming Unit Assay to Quantify Mycobacteria at JoVE.com

Micro-Colony Forming Unit Assay to Quantify Mycobacteria  

Ensayo de la unidad formadora de microcolonias para cuantificar micobacterias

Para realizar la dilución en serie utilizando una placa de pocillos, primero coloque suspensiones de Mycobacterium en las filas A y E de una placa de 96 pocillos. Agregue 180 microlitros de agua desionizada en los pozos restantes para el proceso de dilución en serie. Utilizando una pipeta de 12 canales, vuelva a suspender las suspensiones en la fila A y transfiera 20 microlitros a la fila B.Repita la transferencia de suspensión para las filas B y C hasta que se alcance la última dilución en la fila D.Para el recubrimiento de microgotas, use una pipeta multicanal de 0,5 a 10 microlitros con puntas delgadas para transferir cinco microlitros de cada fila de la placa de 96 pocillos a la placa cuadrada mediana sólida.Deje que las gotas toquen ligeramente el agar, asegurando una transferencia adecuada y minimizando la retención de líquido dentro de la punta. Deje que las gotas se sequen y cierre la placa de agar. Incubarlo a 37 grados centígrados mientras se controla el crecimiento bacteriano.Opcionalmente, coloque las placas de agar en una bolsa de plástico sellada para evitar que se sequen. Después de seis a 10 días de incubación, verifique si hay colonias individuales visibles a simple vista. Coloque la placa bajo un microscopio invertido utilizando el objetivo de aumento más bajo.Alternativamente, use una cámara para tomar una foto de la gota y cuente manualmente las colonias en la computadora usando ImageJ para el conteo automatizado de colonias. Se utilizó la unidad formadora de microcolonias o ensayo micro-UFC para producir grandes cantidades de datos a partir de una pequeña cantidad de placas de agar. El uso de liposomas para la administración de saquinavir aumentó la eficacia del tratamiento contra las cepas de microbacterias con diferentes resistencias a los fármacos.

Research

JoVE Journal

Medicine

Micro-Colony Forming Unit Assay to Quantify Mycobacteria

Micro-Colony Forming Unit Assay for Efficacy Evaluation of Vaccines Against Tuberculosis

Tuberculosis (TB), the leading cause of death worldwide by an infectious agent, killed 1.6 million people in 2022, only being surpassed by COVID-19 during ...

Investigación

Medicina

Bacillus Calmette-Gu&#233;rin (BCG) Vaccine Production

Producción de la vacuna contra el bacilo de Calmette-Guérin (BCG)

Micro-Colony Forming Unit Counting of Mycobacteria Using Fiji &#40;Image J&#41;

Micro-Colony Forming Unit Counting of Mycobacteria Using Fiji (Image J)  

Recuento de unidades formadoras de microcolonias de micobacterias utilizando Fiji (Imagen J)