ERRATUM: Kidney decontamination during perfusion for transplantation procedure: In vitro and ex vivo viability analysis

Organ transplantations have an increasing medical relevance. It is becoming a regular procedure with an increase in individuals waiting for organs. The increase in the number of discarded organs is mostly due to the donor's bacterial and/or viral infection. In this article, we are demonstrating...

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Published inJournal of biophotonics Vol. 16; no. 2; pp. e202200363 - n/a
Main Authors Goenaga‐Mafud, Loraine C., Gamez, Yordania Matos, Campos, Carolina P., Vollet‐Filho, Jose D., Inada, Natalia Mayumi, Kurachi, Cristina, Bagnato, Vanderlei Salvador
Format Journal Article
LanguageEnglish
Published Weinheim WILEY‐VCH Verlag GmbH & Co. KGaA 01.02.2023
Wiley Subscription Services, Inc
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Summary:Organ transplantations have an increasing medical relevance. It is becoming a regular procedure with an increase in individuals waiting for organs. The increase in the number of discarded organs is mostly due to the donor's bacterial and/or viral infection. In this article, we are demonstrating the feasibility of reduction of the bacterial load in the kidney model by using Ultraviolet‐C (UV‐C) as a germicidal agent in circulating liquids. Using Staphylococcus aureus as a bacteria model, we were able to demonstrate that in less than 30 min of liquid circulation and associated to irradiation, the bacterial load of the perfusate Custodiol® HTK, histidine‐tryptophan‐ketoglutarate (solution with 5 log CFU ml−1), was fully eliminated. A modeling approach was created to verify the possibility of bacterial load decrease, when an organ (here, a renal experimental model) is present in the circuit, releasing a varied rate of microorganisms over time, while the solution is irradiated. Finally, we use an ex vivo model with a swine kidney, circulating in the preservation solution with a Lifeport® Kidney Transporter machine, to demonstrate that we can contaminate the organ and then promote the elimination of the microbiological load. The results show the feasibility of the technique. The graphical generally represents the objective of the work, presenting a sequence of experiments as are the final ex vivo studies of the article. Initially, it shows the organ extracted from the pig being perfused in the perfusion machine with contaminated HTK and at the same time this liquid is decontaminated by the UV‐C decontamination system, obtaining results after plating the collected samples to verify bacterial growth.
Bibliography:Funding information
This article corrects JBIO.202100319.
Conselho Nacional de Desenvolvimento Científico e Tecnológico; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Grant/Award Number: 88887.351897/2019‐00; Fundação Amazônia Paraense de Amparo à Pesquisa, Grant/Award Number: CEPOF 2013/07276‐1; Fundação de Apoio à Física e à Química (FAFQ); Organ Recovery Systems, Inc. Company
The part labels of Figure 1 were incorrect. The correct labels and figure caption are presented here.
The authors found calibration errors in the equipment when assessing light fluence rates, which affected the fluence range scales provided in the graphs. The correct data are highlighted in the relevant paragraphs below. The relevance of all findings of the study were preserved, so the conclusions are the same. The only difference is the actual delivered fluence for the investigated times.
Figures 2, 3, 4, 5, and 8 have been modified to reflect the corrections.
erratum
SourceType-Other Sources-1
content type line 63
ObjectType-Correction/Retraction-1
ISSN:1864-063X
1864-0648
DOI:10.1002/jbio.202200363