4.3 Article

Surfactant Treatment for Efficient Gene Detection of Enteric Viruses and Indicators in Surface Water Concentrated by Ultrafiltration

Journal

FOOD AND ENVIRONMENTAL VIROLOGY
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s12560-022-09543-y

Keywords

Enteric virus; Hollow fiber ultrafiltration; RT-PCR inhibition; Sodium deoxycholate; Surface water

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The HFUF-based microbial concentration method is commonly used for monitoring pathogenic viruses and microbial indicators in water samples, but it can co-concentrate substances that interfere with molecular processes. This study evaluated the efficacy of sodium deoxycholate (SD) treatment in mitigating these inhibitory substances. The SD treatment significantly improved the RNA extraction-RT-quantitative PCR efficiency and detection rates of indigenous viruses.
The hollow fiber ultrafiltration (HFUF)-based microbial concentration method is widely applied for monitoring pathogenic viruses and microbial indicators in environmental water samples. However, the HFUF-based method can co-concentrate substances that interfere with downstream molecular processes-nucleic acid extraction, reverse transcription (RT), and PCR. These inhibitory substances are assumed to be hydrophobic and, therefore, expected to be excluded by a simple surfactant treatment before the silica membrane-based RNA extraction process. In this study, the efficacy and limitations of the sodium deoxycholate (SD) treatment were assessed by quantifying a process control and indigenous viruses using 42 surface water samples concentrated with HFUF. With some exceptions, which tended to be seen in samples with high turbidity (> 4.0 NTU), virus recovery by the ultrafiltration method was sufficiently high (> 10%). RNA extraction-RT-quantitative PCR (RTqPCR) efficiency of the process control was insufficient (10%) for 30 of the 42 HFUF concentrates without any pretreatments, but it was markedly improved for 21 of the 30 inhibitory concentrates by the SD treatment. Detection rates of indigenous viruses were also improved and no substantial loss of viral RNA was observed. The SD treatment was particularly effective in mitigating RT-qPCR inhibition, although it was not effective in improving RNA extraction efficiency. The methodology is simple and easily applied. These findings indicate that SD treatment can be a good alternative to sample dilution, which is widely applied to mitigate the effect of RT-qPCR inhibition, and can be compatible with other countermeasures.

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