Evidence map›Paper›PMID 32673355›Full record

ArticlePloS one2020

Ultraviolet A light effectively reduces bacteria and viruses including coronavirus.

Ali Rezaie, Gabriela G S Leite, Gil Y Melmed, Ruchi Mathur, Maria Jesus Villanueva-Millan, Gonzalo Parodi, Jon Sin, Juliana F Germano, Walter Morales, Stacy Weitsman and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. c-di-GMP is a key regulator of Pseudomonas aeruginosa response to UVA radiation.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Article
  2. PrNanomaterials (Basel, Switzerland) · 2025
    Review
  3. Global transcriptional response of Pseudomonas aeruginosa to UVA radiation.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. UV-A Radiation: Safe Human Exposure and Antibacterial Activity.International journal of molecular sciences · 2023
    Article
  10. Linkages between COVID-19, solar UV radiation, and the Montreal Protocol.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Ali RezaieMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.ORCID 0000-0002-0106-372X
Gabriela G S LeiteMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Gil Y MelmedInflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai, Los Angeles, California, United States of America.
Ruchi MathurMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Maria Jesus Villanueva-MillanMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Gonzalo ParodiMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Jon SinCedars-Sinai Heart Institute, Cedars-Sinai, Los Angeles, California, United States of America.
Juliana F GermanoCedars-Sinai Heart Institute, Cedars-Sinai, Los Angeles, California, United States of America.
Walter MoralesMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Stacy WeitsmanMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Seung Young KimDivision of Gastroenterology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, South Korea.ORCID 0000-0001-8933-7715
Jae Ho ParkDivision of Gastroenterology, Department of Internal Medicine, Ulsan University Hospital, Ulsan, South Korea.
Siamak SakhaieAustralian Clinical Labs, Melbourne, Australia.
Mark PimentelMedically Associated Science and Technology (MAST) Program, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Cedars-Sinai Medical Center · USKorea University · KRUlsan University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial-resistant and novel pathogens continue to emerge, outpacing efforts to contain and treat them. Therefore, there is a crucial need for safe and effective therapies. Ultraviolet-A (UVA) phototherapy is FDA-approved for several dermatological diseases but not for internal applications. We investigated UVA effects on human cells in vitro, mouse colonic tissue in vivo, and UVA efficacy against bacteria, yeast, coxsackievirus group B and coronavirus-229E. Several pathogens and virally transfected human cells were exposed to a series of specific UVA exposure regimens. HeLa, alveolar and primary human tracheal epithelial cell viability was assessed after UVA exposure, and 8-Oxo-2'-deoxyguanosine was measured as an oxidative DNA damage marker. Furthermore, wild-type mice were exposed to intracolonic UVA as an in vivo model to assess safety of internal UVA exposure. Controlled UVA exposure yielded significant reductions in Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Enterococcus faecalis, Clostridioides difficile, Streptococcus pyogenes, Staphylococcus epidermidis, Proteus mirabilis and Candida albicans. UVA-treated coxsackievirus-transfected HeLa cells exhibited significantly increased cell survival compared to controls. UVA-treated coronavirus-229E-transfected tracheal cells exhibited significant coronavirus spike protein reduction, increased mitochondrial antiviral-signaling protein and decreased coronavirus-229E-induced cell death. Specific controlled UVA exposure had no significant effect on growth or 8-Oxo-2'-deoxyguanosine levels in three types of human cells. Single or repeated in vivo intraluminal UVA exposure produced no discernible endoscopic, histologic or dysplastic changes in mice. These findings suggest that, under specific conditions, UVA reduces various pathogens including coronavirus-229E, and may provide a safe and effective treatment for infectious diseases of internal viscera. Clinical studies are warranted to further elucidate the safety and efficacy of UVA in humans.

Indexed as

AnimalsApoptosisBacteriaBacterial InfectionsCell SurvivalColonCoronavirus 229E, HumanDisease Models, AnimalDNA DamageEnterovirus B, HumanFemaleHeLa CellsHumansIntestinal MucosaMaleMice

Identifiers

PMID32673355
PMCPMC7365468
OpenAlexW3042271358

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.