Optimization of PMAxx pretreatment to distinguish between human norovirus with intact and altered capsids in shellfish and sewage samples
|Author(s)||Randazzo Walter1, 2, Khezri Mohammad3, Ollivier Joanna4, Le Guyader Soizick4, Rodriguez-Diaz Jesus1, 5, Aznar Rosa1, 2, Sanchez Gloria2|
|Affiliation(s)||1 : Univ Valencia, Dept Microbiol & Ecol, Av Dr Moliner 50, E-46100 Valencia, Spain.
2 : CSIC, IATA, Dept Preservat & Food Safety Technol, Av Agustin Escardino 7, Valencia 46980, Spain.
3 : Tarbiat Modares Univ, Fac Marine Sci, Dept Seafood Proc, Noor, Iran.
4 : IFREMER, LSEM SG2M, Lab Microbiol, BP 21105, F-44311 Nantes 03, France.
5 : INCLIVA, Hosp Clin Univ, Inst Clin Res, Valencia, Spain.
|Source||International Journal Of Food Microbiology (0168-1605) (Elsevier Science Bv), 2018-02 , Vol. 266 , P. 1-7|
|WOS© Times Cited||59|
|Keyword(s)||Intercalating dyes, Viability PCR, Norovirus, Shellfish, Sewage, RT-qPCR|
Shellfish contamination by human noroviruses (HuNoVs) is a serious health and economic problem. Recently an ISO procedure based on RT-qPCR for the quantitative detection of HuNoVs in shellfish has been issued, but these procedures cannot discriminate between inactivated and potentially infectious viruses. The aim of the present study was to optimize a pretreatment using PMAxx to better discriminate between intact and heat-treated HuNoVs in shellfish and sewage. To this end, the optimal conditions (30 min incubation with 100 μM of PMAxx and 0.5% of Triton, and double photoactivation) were applied to mussels, oysters and cockles artificially inoculated with thermally-inactivated (99 °C for 5 min) HuNoV GI and GII. This pretreatment reduced the signal of thermally-inactivated HuNoV GI in cockles and HuNoV GII in mussels by > 3 log. Additionally, this pretreatment reduced the signal of thermally-inactivated HuNoV GI and GII between 1 and 1.5 log in oysters. Thermal inactivation of HuNoV GI and GII in PBS, sewage and bioaccumulated oysters was also evaluated by the PMAxx-Triton pretreatment. Results showed significant differences between reductions observed in the control and PMAxx-treated samples in PBS following treatment at 72 and 95 °C for 15 min. In sewage, the RT-qPCR signal of HuNoV GI was completely removed by the PMAxx pretreatment after heating at 72 and 95 °C, while the RT-qPCR signal for HuNoV GII was completely eliminated only at 95 °C.
Finally, the PMAxx-Triton pretreatment was applied to naturally contaminated sewage and oysters, resulting in most of the HuNoV genomes quantified in sewage and oyster samples (12 out of 17) corresponding to undamaged capsids. Although this procedure may still overestimate infectivity, the PMAxx-Triton pretreatment represents a step forward to better interpret the quantification of intact HuNoVs in complex matrices, such as sewage and shellfish, and it could certainly be included in the procedures based on RT-qPCR.