- A new recombinant plasmid, pGU2664, stably expresses the highly ﬂuorescent GFPmut3 biomarker in GBS
- The GFPmut3 biomarker can be successfully applied to track the growth of bacteria in liquid media
- CLARIOstar® acquires absorbance, ﬂuorescence and polarized ﬂuorescence to characterize GFPmut3 GBS
Table of contents
Streptococcus agalactiae (also known as group B streptococcus [GBS]) is associated with various diseases and infections in humans and animals.1 These include neonatal disease, sepsis, arthritis, pneumonia, meningitis, skin and soft tissue infections such as urinary tract infection.
Research efforts focused on the mechanisms for host colonization and virulence have mainly utilized microscopy techniques coupled with ﬂuorescent biomarkers. Strategies for labelling GBS with ﬂuorescent biomarkers, have so far been limited to antibody-based immunostaining methods and nonspeciﬁc protein/DNA stains.
Green ﬂuorescent protein (GFP) expression is a common labeling method for the study of bacteria. It enables the identiﬁcation of bacteria in complex samples, the monitoring of subcellular locations of bacteria in eukaryotic host cells, and the development of novel and efﬁcient enumeration methods such as based on ﬂow cytometry.
In a recent study1 we have reported stable expression of a green ﬂuorescent protein mutant (GFPmut3) in GBS. This was achieved through the use of GFP-variant-expressing plasmid, pGU2664. GFPmut3 has 20x greater ﬂuorescence intensity than GFP, allowing greater sensitivity for visualization of GBS2. Herein, we describe absorbance, ﬂuorescence and ﬂuorescence polarisation intensity experiments aimed at validating and monitoring the stability of GFPmut3 expression in GBS cultures. A detailed account of microscopic analysis, effect of antimicrobials on GFPmut3 expression in GBS and adhesion studies of GFP-expressing GBS to human epithelial cells is described in Applied and Environmental Microbiology1.
Polarised ﬂuorescence intensity
Fluorescence polarisation measures rotation of molecules in solution. High molecular weight species (like GFP) rotate slowly and when excited with plane polarised light emit a high proportion of polarised light back to the detector. Low molecular weight compounds rotate quickly and re-emit unpolarised light. The degree of polarisation (P), is deﬁned as (Ipara - Iperp) / (Ipara+ Iperp), where Ipara is the ﬂuorescence intensity measured parallel and Iperp is that measured perpendicular to the plane of polarization of the excitation light.
For slow rotating species in solution the Polarisation value can be as high as 0.4 (400mP). For low molecular weight, quickly rotating molecules this value is very low (35mP or less) because Ipara-Iperp gives a very small value in the above equation due to the intensities being very nearly the same. In our study, we have made use of this property to monitor GFPmut3 ﬂuorescence over background autoﬂuorescence in the commonly used bacterial medium for growth of GBS, Todd-Hewitt Broth (THB). Polarisation intensities, Ipara and Iperp, were measured temporally over a 12-hour period and total ﬂuorescence polarisation intensity was calculated by the sum Ipara+2Iperp.
Material & Methods
- Microplates (96 well, Greiner Cat No. 655185)
- CLARIOstar with atmospheric control unit (ACU)
- Plates were sealed using gas-permeable BreatheEasy membranes (Sigma, Cat No. Z380059)
Overnight THB cultures of GBS str 874391 were harvested by centrifugation (8,000 x g, 10 min) and washed three times with PBS (pH 7.4). Bacteria were subsequently diluted 1:100 into fresh Chemically Deﬁned Medium (CDM) or THB (approx. 1x106 CFU per well) and 200 ul volumes of the cell suspensions were aliquoted in triplicate into wells of a 96 well plate.
Plates were sealed with breathe-easy membrane and incubated for 12h in the CLARIOstar multi-mode microplate reader, with temperature set to 37 °C and a 5 % CO2 atmosphere.
|Discrete wavelength||600 nm|
|Pathlength correction||200 µl|
|Fluorescence Polarization (FP)|
|Filters||Ex 482-16 |
|Gains||A: 951; B 1113|
|General settings||Number of flashes||10, 50 for FP|
|Settling time||0.2 s|
|Orbital averaging||3 mm|
|Kinetic settings||Number of cycles||74|
|Cycle time||900 s|
|Atmospheric Control||CO2: 5%; O2: monitoring|
Results & Discussion
The GFPmut3 plasmid pGU2664 was introduced, via electroporation, into GBS 874391 to create GBS strain GU2666 (GFP+). In addition, a non-GFPmut3 vector was introduced to create strain GU2672 (GFP-).1
GBS containing the empty vector (GFP-), suggesting no signiﬁcant metabolic burden to the GBS strain carrying the pGU2664 plasmid (Fig. 1A). In addition, there was strong GFP emission that correlated well with cell density, demonstrating expression and stability of GFPmut3 across exponential and stationary growth phases (Fig. 1B).
The ﬂuorescence of GFPmut3 was also examined under stationary phase and low nutrient conditions. Cells were grown overnight, re-suspended in PBS and monitored for turbidity and ﬂuorescence over 12h, as described above. We observed stable and high-level ﬂuorescence for these stationary phase populations with turbidity remaining stable (Fig 1, C &D).
THB is a standard complete media commonly used for growing GBS for infection experiments in animal or cell culture-based methods. We therefore also investigated the expression of GFPmut3 ﬂuorescence during growth in THB. Interestingly, the THB media contains compounds that autoﬂuoresce at 515nm, which interfere with the GFP signal (Fig 2B). This could be conveniently overcome by montoring GBS growth via polarised ﬂuorescence intensity over the 12 hour period (Fig 2C).
Taken together, the above results demonstrate a new method for analyzing GFPmut3 expressing GBS in experimental systems, emphasising the usefulness of the FP intensity monitoring technique in microbiology.
This study also highlights the versatility of the CLARIOstar multi-mode plate reader with ACU for microbiology. The instrument can incubate and shake samples under a controlled atmosphere (CO2 and/or O2) while acquiring data using various techniques (Fl, Lum, Abs, FP) simultaneously. In our laboratory, this has become an essential tool for investigating bacterial survival and the mechanisms of infection.
1. Sullivan, MJ, Ulett, GC. Applied Environmental Microbiology. (2018) 84: 1-18. DOI: 10.1128/AEM.01262-18.
2. Cormack BP et al. Gene (1996) 173: 33-38. DOI: 10.1016/0378-1119(95)00685-0 *Copyright © American Society for Microbiology, Applied and Environmental Microbiology, 84 (18), 2018, e01262-18