TY - JOUR
T1 - Detection and quantification of poliovirus infection using FTIR spectroscopy and cell culture
AU - Lee-Montiel, Felipe T.
AU - Reynolds, Kelly A.
AU - Riley, Mark R.
N1 - Funding Information:
FLM was funded by a CONACYT fellowship. This work was supported in part by the NIEHS sponsored Southwest Environmental Health Sciences Center #P30 ES06694. Dr. Charles Gerba and Dr. Kelly Reynolds generously provided purified vaccine strain poliovirus type 1 (PV1, LSc-2ab), at University of Arizona. Doug Cromey and Dr. Brooke Beam helped with the confocal images and Jonathan Sexton assisted with CPE analysis of the virus samples used in the development of this method.
PY - 2011/12/5
Y1 - 2011/12/5
N2 - Background: In a globalized word, prevention of infectious diseases is a major challenge. Rapid detection of viable virus particles in water and other environmental samples is essential to public health risk assessment, homeland security and environmental protection. Current virus detection methods, especially assessing viral infectivity, are complex and time-consuming, making point-of-care detection a challenge. Faster, more sensitive, highly specific methods are needed to quantify potentially hazardous viral pathogens and to determine if suspected materials contain viable viral particles. Fourier transform infrared (FTIR) spectroscopy combined with cellular-based sensing, may offer a precise way to detect specific viruses. This approach utilizes infrared light to monitor changes in molecular components of cells by tracking changes in absorbance patterns produced following virus infection. In this work poliovirus (PV1) was used to evaluate the utility of FTIR spectroscopy with cell culture for rapid detection of infective virus particles.Results: Buffalo green monkey kidney (BGMK) cells infected with different virus titers were studied at 1 - 12 hours post-infection (h.p.i.). A partial least squares (PLS) regression method was used to analyze and model cellular responses to different infection titers and times post-infection. The model performs best at 8 h.p.i., resulting in an estimated root mean square error of cross validation (RMSECV) of 17 plaque forming units (PFU)/ml when using low titers of infection of 10 and 100 PFU/ml. Higher titers, from 10 3 to 10 6 PFU/ml, could also be reliably detected.Conclusions: This approach to poliovirus detection and quantification using FTIR spectroscopy and cell culture could potentially be extended to compare biochemical cell responses to infection with different viruses. This virus detection method could feasibly be adapted to an automated scheme for use in areas such as water safety monitoring and medical diagnostics.
AB - Background: In a globalized word, prevention of infectious diseases is a major challenge. Rapid detection of viable virus particles in water and other environmental samples is essential to public health risk assessment, homeland security and environmental protection. Current virus detection methods, especially assessing viral infectivity, are complex and time-consuming, making point-of-care detection a challenge. Faster, more sensitive, highly specific methods are needed to quantify potentially hazardous viral pathogens and to determine if suspected materials contain viable viral particles. Fourier transform infrared (FTIR) spectroscopy combined with cellular-based sensing, may offer a precise way to detect specific viruses. This approach utilizes infrared light to monitor changes in molecular components of cells by tracking changes in absorbance patterns produced following virus infection. In this work poliovirus (PV1) was used to evaluate the utility of FTIR spectroscopy with cell culture for rapid detection of infective virus particles.Results: Buffalo green monkey kidney (BGMK) cells infected with different virus titers were studied at 1 - 12 hours post-infection (h.p.i.). A partial least squares (PLS) regression method was used to analyze and model cellular responses to different infection titers and times post-infection. The model performs best at 8 h.p.i., resulting in an estimated root mean square error of cross validation (RMSECV) of 17 plaque forming units (PFU)/ml when using low titers of infection of 10 and 100 PFU/ml. Higher titers, from 10 3 to 10 6 PFU/ml, could also be reliably detected.Conclusions: This approach to poliovirus detection and quantification using FTIR spectroscopy and cell culture could potentially be extended to compare biochemical cell responses to infection with different viruses. This virus detection method could feasibly be adapted to an automated scheme for use in areas such as water safety monitoring and medical diagnostics.
KW - Buffalo green monkey kidney (bgmk) cells
KW - Cell culture
KW - Enterovirus
KW - Fourier transform infrared (ftir) spectroscopy
KW - Mid-infrared
KW - Partial least squares
KW - Poliovirus (pv1)
KW - Virus detection
KW - Zinc selenide (znse)
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U2 - 10.1186/1754-1611-5-16
DO - 10.1186/1754-1611-5-16
M3 - Article
C2 - 22142483
AN - SCOPUS:82655170559
SN - 1754-1611
VL - 5
JO - Journal of Biological Engineering
JF - Journal of Biological Engineering
M1 - 16
ER -