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Removal of Hepatitis B virus surface HBsAg and core HBcAg antigens using microbial fuel cells producing electricity from human urine
Authors
Agnieszka Solak
Andrea Goglio
+43 more
Anthony J. Slate
B Kołwzan
Benjamin Erable
Benjamin Erable
Carolina Cruz Viggi
Chin-Tsan Wang
Clement A. Cid
DA Jadhav
Elena Kipf
ES Heidrich
G Chen
G Pasternak
G Pasternak
G Pasternak
G Pasternak
H Kobayashi
HP Bennetto
I Ieropoulos
Ioannis Andrea Ieropoulos
J.J. Ott
Jayesh M. Sonawane
JL Pousset
Lydia S. Y. Tang
M Behera
M Knutsson
M.J Salar-García
ME Hernandez
Mohammadreza Kamali
MR Dyson
N Nath
N Zelver
Nelly Gonzalez‐Rivas
Qinzheng Yang
RD Cusick
S Jung
Sara Mateo
Siti Mariam Daud
T Amani
T.-T. Fong
W-W Li
WOK Grabow
X Zhou
Yonggang Yang
Publication date
13 August 2019
Publisher
'Springer Science and Business Media LLC'
Doi
Abstract
© 2019, The Author(s). Microbial electrochemical technology is emerging as an alternative way of treating waste and converting this directly to electricity. Intensive research on these systems is ongoing but it currently lacks the evaluation of possible environmental transmission of enteric viruses originating from the waste stream. In this study, for the first time we investigated this aspect by assessing the removal efficiency of hepatitis B core and surface antigens in cascades of continuous flow microbial fuel cells. The log-reduction (LR) of surface antigen (HBsAg) reached a maximum value of 1.86 ± 0.20 (98.6% reduction), which was similar to the open circuit control and degraded regardless of the recorded current. Core antigen (HBcAg) was much more resistant to treatment and the maximal LR was equal to 0.229 ± 0.028 (41.0% reduction). The highest LR rate observed for HBsAg was 4.66 ± 0.19 h−1 and for HBcAg 0.10 ± 0.01 h−1. Regression analysis revealed correlation between hydraulic retention time, power and redox potential on inactivation efficiency, also indicating electroactive behaviour of biofilm in open circuit control through the snorkel-effect. The results indicate that microbial electrochemical technologies may be successfully applied to reduce the risk of environmental transmission of hepatitis B virus but also open up the possibility of testing other viruses for wider implementation
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Southampton (e-Prints Soton)
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oai:eprints.soton.ac.uk:456364
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