Human milk inhibits some enveloped virus infections, including SARS-CoV-2, in an intestinal model

被引:12
作者
Aknouch, Ikrame [1 ,2 ,3 ]
Sridhar, Adithya [1 ,2 ]
Freeze, Eline [1 ,2 ]
Giugliano, Francesca Paola [4 ]
van Keulen, Britt J. [5 ]
Romijn, Michelle [5 ]
Calitz, Carlemi [1 ,2 ]
Garcia-Rodriguez, Ines [1 ,2 ]
Mulder, Lance [1 ,2 ]
Wildenberg, Manon E. [4 ]
Muncan, Vanesa [4 ]
van Gils, Marit J. [6 ]
van Goudoever, Johannes B. [5 ]
Stittelaar, Koert J. [7 ]
Wolthers, Katja C. [1 ]
Pajkrt, Dasja [2 ]
机构
[1] Univ Amsterdam, Amsterdam UMC, Amsterdam Inst Infect & Immun, Dept Med Microbiol,OrganoVIR Labs, Amsterdam, Netherlands
[2] Univ Amsterdam, Vrije Univ, Amsterdam UMC, Emma Childrens Hosp,Dept Pediat Infect Dis, Amsterdam, Netherlands
[3] Viroclin Xplore, Schaijk, Netherlands
[4] Univ Amsterdam, Amsterdam UMC, Tytgat Inst Intestinal & Liver Res, Amsterdam Gastroenterol Endocrinol & Metab, Amsterdam, Netherlands
[5] Univ Amsterdam, Amsterdam UMC, Vrije Univ,Dept Pediat, Emma Childrens Hosp,Dutch Natl Human Milk Bank, Amsterdam, Netherlands
[6] Univ Amsterdam, Amsterdam UMC, Amsterdam Inst Infect & Immun, Dept Med Microbiol, Amsterdam, Netherlands
[7] Wageningen Univ, Dept Epidemiol Bioinformat & Anim Models, Wageningen Biovet Res, Wageningen, Netherlands
基金
欧盟地平线“2020”;
关键词
IN-VITRO; LACTOFERRIN; TRANSMISSION; PROTEINS; HIV;
D O I
10.26508/lsa.202201432
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human milk is important for antimicrobial defense in infants and has well demonstrated antiviral activity. We evaluated the protective ability of human milk against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in a human fetal intestinal cell culture model. We found that, in this model, human milk blocks SARS-CoV-2 replication, irrespective of the presence of SARS-CoV-2 spike-specific antibodies. Complete inhibition of both enveloped Middle East respiratory syndrome coronavirus and human respiratory syncytial virus infections was also observed, whereas no inhibition of non-enveloped enterovirus A71 infection was seen. Transcriptome analysis after 24 h of the intestinal monolayers treated with human milk showed large transcriptomic changes from human milk treatment, and subsequent analysis suggested that ATP1A1 down-regulation by milk might be of importance. Inhibition of ATP1A1 blocked SARS-CoV-2 infection in our intestinal model, whereas no effect on EV-A71 infection was seen. Our data indicate that human milk has potent antiviral activity against particular (enveloped) viruses by potentially blocking the ATP1A1-mediated endocytic process.
引用
收藏
页数:15
相关论文
共 80 条
[1]   ELECTROLYTE AND PH CHANGES IN HUMAN MILK [J].
ANSELL, C ;
MOORE, A ;
BARRIE, H .
PEDIATRIC RESEARCH, 1977, 11 (12) :1177-1179
[2]   Cellular host factors for SARS-CoV-2 infection [J].
Baggen, Jim ;
Vanstreels, Els ;
Jansen, Sander ;
Daelemans, Dirk .
NATURE MICROBIOLOGY, 2021, 6 (10) :1219-1232
[3]   Ouabain-like compound changes rapidly on physical exercise in humans and dogs -: Effects of β-blockade and angiotensin-converting enzyme inhibition [J].
Bauer, N ;
Müller-Ehmsen, J ;
Krämer, U ;
Hambarchian, N ;
Zobel, C ;
Schwinger, RHG ;
Neu, H ;
Kirch, U ;
Grünbaum, EG ;
Schoner, W .
HYPERTENSION, 2005, 45 (05) :1024-1028
[4]   SARS-CoV-2 RNA and antibody detection in breast milk from a prospective multicentre study in Spain [J].
Bauerl, Christine ;
Randazzo, Walter ;
Sanchez, Gloria ;
Selma-Royo, Marta ;
Garcia Verdevio, Elia ;
Martinez, Laura ;
Parra-Llorca, Anna ;
Lerin, Carles ;
Fumado, Victoria ;
Crovetto, Francesca ;
Crispi, Fatima ;
Perez-Cano, Francisco J. ;
Rodriguez, Gerardo ;
Ruiz-Redondo, Gemma ;
Campoy, Cristina ;
Martinez-Costa, Cecilia ;
Carmen Collado, Maria .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2022, 107 (02) :216-221
[5]   Characterization of the anti-HIV effects of native lactoferrin and other milk proteins and protein-derived peptides [J].
Berkhout, B ;
van Wamel, JLB ;
Beljaars, L ;
Meijer, DKF ;
Visser, S ;
Floris, R .
ANTIVIRAL RESEARCH, 2002, 55 (02) :341-355
[6]   Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability [J].
Brouwer, Philip J. M. ;
Caniels, Tom G. ;
van der Straten, Karlijn ;
Snitselaar, Jonne L. ;
Aldon, Yoann ;
Bangaru, Sandhya ;
Torres, Jonathan L. ;
Okba, Nisreen M. A. ;
Claireaux, Mathieu ;
Kerster, Gius ;
Bentlage, Arthur E. H. ;
van Haaren, Marlies M. ;
Guerra, Denise ;
Burger, Judith A. ;
Schermer, Edith E. ;
Verheul, Kirsten D. ;
van der Velde, Niels ;
van der Kooi, Alex ;
van Schooten, Jelle ;
van Breemen, Marielle J. ;
Bijl, Tom P. L. ;
Sliepen, Kwinten ;
Aartse, Aafke ;
Derking, Ronald ;
Bontjer, Ilja ;
Kootstra, Neeltje A. ;
Wiersinga, W. Joost ;
Vidarsson, Gestur ;
Haagmans, Bart L. ;
Ward, Andrew B. ;
de Bree, Godelieve J. ;
Sanders, Rogier W. ;
van Gils, Marit J. .
SCIENCE, 2020, 369 (6504) :643-+
[7]   ATP1A1-Mediated Src Signaling Inhibits Coronavirus Entry into Host Cells [J].
Burkard, Christine ;
Verheije, Monique H. ;
Haagmans, Bart L. ;
van Kuppeveld, Frank J. ;
Rottier, Peter J. M. ;
Bosch, Berend-Jan ;
de Haan, Cornelis A. M. .
JOURNAL OF VIROLOGY, 2015, 89 (08) :4434-4448
[8]   Annexin A1 as a potential prognostic biomarker for COVID-19 disease: Case-control study [J].
Canacik, Omer ;
Sabirli, Ramazan ;
Altintas, Emel ;
Karsli, Emre ;
Karis, Denizhan ;
Kaymaz, Buse ;
Sabirli, Gizem Tukenmez ;
Kurt, Ozgur ;
Koseler, Aylin .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2021,
[9]   Transmission of SARS-CoV-2 through breast milk and breastfeeding: a living systematic review [J].
Centeno-Tablante, Elizabeth ;
Medina-Rivera, Melisa ;
Finkelstein, Julia L. ;
Rayco-Solon, Pura ;
Garcia-Casal, Maria Nieves ;
Rogers, Lisa ;
Ghezzi-Kopel, Kate ;
Ridwan, Pratiwi ;
Pena-Rosas, Juan Pablo ;
Mehta, Saurabh .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 2021, 1484 (01) :32-54
[10]   Evaluation for SARS-CoV-2 in Breast Milk From 18 Infected Women [J].
Chambers, Christina ;
Krogstad, Paul ;
Bertrand, Kerri ;
Contreras, Deisy ;
Tobin, Nicole H. ;
Bode, Lars ;
Aldrovandi, Grace .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 324 (13) :1347-1348