Effect of High Hydrostatic Pressure Processing and Holder Pasteurization of Human Milk on Inactivation of Human Coronavirus 229E and Hepatitis E Virus

被引:4
|
作者
Bouquet, Peggy [1 ]
Alexandre, Virginie [2 ]
De Lamballerie, Marie [3 ]
Ley, Delphine [4 ,5 ]
Lesage, Jean [5 ]
Goffard, Anne [1 ,2 ]
Cocquerel, Laurence [2 ]
机构
[1] Inst Pasteur, Unit Clin Microbiol, F-59000 Lille, France
[2] Univ Lille, CHU Lille, INSERM, CIIL Ctr forInfect Immun Lille,CNRS,Inst Pasteur L, F-59000 Lille, France
[3] UMR CNRS 6144, GEPEA, ONIRIS CS 82225, F-44322 Nantes, France
[4] CHU Lille, Jeanne de Flandre Childrens Hosp, Dept Paediat, Div Gastroenterol Hepatol & Nutr, F-59000 Lille, France
[5] Univ Lille, CHU Lille, INSERM, INFIN Inst Translat Res Inflammat,U1286, F-59000 Lille, France
来源
VIRUSES-BASEL | 2023年 / 15卷 / 07期
关键词
human milk; high hydrostatic pressure; Holder pasteurization; coronavirus; hepatitis E virus; infectivity;
D O I
10.3390/v15071571
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In preterm infants, sterilized donor milk (DM) is frequently used for feeding when breast milk is lacking. Most human milk banks use the Holder pasteurization method (HoP) to ensure the microbiological safety of DM. However, this method degrades many bioactive factors and hormones. Recently, high hydrostatic pressure (HHP) processing, which preserves bioactive factors in human milk, has been proposed as an alternative method to ensure the safety of DM. Although HHP treatment has been shown to be effective for viral inactivation, the effect of HHP on viruses that may be present in the complex nutritional matrix of human milk has not yet been defined. In the present study, we compared the efficacy of two HHP protocols (4 cycles at 350 MPa at 38 & DEG;C designated as 4xHP350 treatment, and 1 cycle at 600 MPa at 20 & DEG;C designated as 1xHP600 treatment) with the HoP method on artificially virus-infected DM. For this purpose, we used human coronavirus 229E (HCoV-229E) and hepatitis E virus (HEV) as surrogate models for enveloped and non-enveloped viruses. Our results showed that HCoV-229E is inactivated by HHP and HoP treatment. In particular, the 4xHP350 protocol is highly effective in inactivating HCoV-229E. However, our results demonstrated a matrix effect of human milk on HCoV-229E inactivation. Furthermore, we demonstrated that HEV is stable to moderate pressure HHP treatment, but the milk matrix does not protect it from inactivation by the high-pressure HHP treatment of 600 MPa. Importantly, the complex nutritional matrix of human milk protects HEV from inactivation by HoP treatment. In conclusion, we demonstrated that HHP and HoP treatments do not lead to complete inactivation of both surrogate virus models, indicating that these treatments cannot guarantee total viral safety of donor milk.
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页数:13
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