Jesus L. Lucina Romero-Romero

Dr. Jesus L. Lucina Romero-Romero


Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 June 2022 in Pathogens
Verified
Journal Article
Open access
PDF file
VSViviana Andrea Sosa-Zuniga
Viviana Andrea Sosa-Zuniga
AVAlvaro Ignacio Vidal Valenzuela
Alvaro Ignacio Vidal Valenzuela
PBPaola Barba
Paola Barba
CCCarmen Espinoza Cancino
Carmen Espinoza Cancino
JRJesus L. Lucina Romero-Romero
Jesus L. Lucina Romero-Romero
PAPatricio Arce-Johnson
Patricio Arce-Johnson
Grapevine (Vitis vinifera) is one of the main fruit crops worldwide. In 2020, the total surface area planted with vines was estimated at 7.3 million hectares. Diverse pathogens affect grapevine yield, fruit, and wine quality of which powdery mildew is the most important disease prior to harvest. Its causal agent is the biotrophic fungus Erysiphe necator, which generates a decrease in cluster weight, delays fruit ripening, and reduces photosynthetic and transpiration rates. In addition, powdery mildew induces metabolic reprogramming in its host, affecting primary metabolism. Most commercial grapevine cultivars are highly susceptible to powdery mildew; consequently, large quantities of fungicide are applied during the productive season. However, pesticides are associated with health problems, negative environmental impacts, and high costs for farmers. In paralleled, consumers are demanding more sustainable practices during food production. Therefore, new grapevine cultivars with genetic resistance to powdery mildew are needed for sustainable viticulture, while maintaining yield, fruit, and wine quality. Two main gene families confer resistance to powdery mildew in the Vitaceae, Run (Resistance to Uncinula necator) and Ren (Resistance to Erysiphe necator). This article reviews the powdery mildew resistance genes and loci and their use in grapevine breeding programs.

28 March 2025
Verified
Book Chapter
Closed access
PDF file
JRJesus L. Lucina Romero-Romero
Jesus L. Lucina Romero-Romero
ACAgnes Cadavid-Labrada
Agnes Cadavid-Labrada
RTRodrigo Tamayo
Rodrigo Tamayo
PAPatricio Arce-Johnson
Patricio Arce-Johnson

22 May 2026 in Antioxidants
Verified
Journal Article
Open access
PDF file
PAPatricio Arce-Johnson
Patricio Arce-Johnson
YRYohaily Rodríguez-Alvarez
Yohaily Rodríguez-Alvarez
CSCarolina Gabriela Vallejos Sierra
Carolina Gabriela Vallejos Sierra
JRJesus L. Lucina Romero-Romero
Jesus L. Lucina Romero-Romero
LMLuisbel González Pérez de Medina
Luisbel González Pérez de Medina
Alain Manuel Chaple-GilAlain Manuel Chaple-Gil
Alain Manuel Chaple-Gil
Aristotelia chilensis (maqui berry) is a Chilean native fruit rich in anthocyanins with potential antioxidant, glycemic, cardiometabolic, and ocular benefits, but its clinical efficacy remains unclear. This systematic review synthesized and critically appraised human trials evaluating oral maqui supplementation in adults. Following PRISMA 2020 and a PROSPERO-registered protocol, five databases were searched, and risk of bias and certainty of evidence were assessed using RoB 2/ROBINS-I and GRADE. Twelve clinical trials published between 2014 and 2023 were included. Acute studies consistently showed reduced postprandial glucose and modulation of insulin response, whereas chronic interventions showed modest and inconsistent effects on HbA1c, lipid profile, and other cardiometabolic markers. Favorable changes were also reported for oxidative stress biomarkers and autonomic parameters, although these findings were mainly based on surrogate endpoints. The most consistent evidence was observed in the ocular domain, where maqui supplementation improved tear production, dry eye symptoms, and tear inflammatory markers. The overall certainty of evidence ranged from moderate to very low because of methodological heterogeneity, small sample sizes, and short intervention duration. Maqui berry supplementation shows promise, particularly for acute glycemic control and ocular surface health, but larger long-term randomized trials using standardized formulations are needed before definitive clinical recommendations can be made.