Elsa Gladys Aguilar Ancori

Prof. Elsa Gladys Aguilar Ancori

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

View All Publications
12 August 2018 in Journal of Fungi
Verified
Journal Article
Open access
PDF file
Max Carlos Ramírez-SotoMax Carlos Ramírez-Soto
Max Carlos Ramírez-Soto
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori
ATAndrés Tirado-Sánchez
Andrés Tirado-Sánchez
ABAlexandro Bonifaz
Alexandro Bonifaz
Ecological determinants of sporotrichosis etiological agents remain poorly understood. For this reason, we performed explorations using local climate estimates to determine the temperature and humidity ranges of the environment where clinically relevant Sporothrix species occur and to identify what plant species are associated with them, using data collected from the published literature. We performed a literature search to identify all publications on environmental isolations of medically relevant species of Sporothrix in the PubMed, SCOPUS, and EMBASE databases. All those studies were included in the analysis where medically relevant species of Sporothrix have been isolated from soil samples, and described a specific geographical location that could be precisely georeferenced. We approximated temperature and humidity from local climate estimates, integrating geospatial data, temperature, and water vapor pressure from regions or provinces where medically relevant species of Sporothrix have been isolated from soil. Sporothrix spp. were more commonly isolated from soil of different regions or provinces of 16 countries. Most environmental isolates were identified as S. schenckii, whereas S. pallida, S. brasiliensis, S. globosa, and S. mexicana were rare. We estimate that medically relevant Sporothrix spp. grow in the soil at temperatures of 6.6 °C to 28.84 °C and 37.5% to 99.06% relative humidity. These findings indicate that sporotrichosis etiological agents grow in soil in ecological niches from soil with wide ranges of temperature and humidity, but they are also associated with a variety of plants, flowers, woody debris, reed leaves, corn stalks, leaves, and wood crumbs, potentially facilitating its establishment and proliferation in the environment.

28 April 2025 in Scientific Reports
Verified
Journal Article
Open access
PDF file
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori
MMMarishani Marin-Carrasco
Marishani Marin-Carrasco
LCLaura Isabel Campo-Pfuyo
Laura Isabel Campo-Pfuyo
JMJulia Griselda Muñiz-Duran
Julia Griselda Muñiz-Duran
AEAbraham Espinoza-Culupú
Abraham Espinoza-Culupú
Multidrug-resistant Klebsiella pneumoniae (MDR K. pneumoniae) is a significant pathogen associated with nosocomial infections, often leading to high morbidity and mortality. This resistance is largely due to the efficient horizontal transfer of mobile genetic elements such as plasmids, which carry resistance genes and virulence factors. These elements contribute to the production of extended-spectrum β-lactamases (ESBL) and carbapenemases, which further complicates treatment. Despite the high prevalence of MDR K. pneumoniae in Peruvian hospitals, the genomic characterization of these strains remains limited. This study investigated the phenotypic and molecular identification of extended-spectrum β-lactamases (ESBLs), carbapenemases, and virulence factors in 91 MDR K. pneumoniae strains collected from three hospitals between 2022 and 2023. Phenotypic detection of ESBLs was performed using the Jarlier method, while carbapenemases were identified via double-disk synergy testing with boronic acid, EDTA, and Carba NP test. The positive isolates were further analyzed for resistance genes (blaCTX-M, blaTEM, blaSHV, blaKPC, blaNDM, blaIMP, and blaVIM). Four isolates were subjected to whole-genome sequencing (WGS) for further characterization. All multidrug-resistant K. pneumoniae strains (100%) were ESBL-positive, with 14.3% producing carbapenemases, primarily KPC-type and metallo-β-lactamases (MBLs). The virulence factor analyses revealed that only 7.7% exhibited hypermucoviscosity. Protease activity was detected in 19.8% of the strains, and lipase activity in 1.1%. Regarding biofilm formation, 85.7% of the strains showed moderate adherence. Molecular analysis identified ESBL (blaCTX-M, 78%; blaTEM, 71.4%; blaSHV, 82.4%) and carbapenemase genes (blaKPC 7.7%, blaNDM 4.4%). Genomic analysis revealed various antimicrobial resistance mechanisms, including porin-coding gene mutations, aminoglycoside resistance linked to fluoroquinolone resistance, and multidrug efflux pump regulators. Sequence typing has identified high-risk clones (ST147, ST629, and ST37) associated with hospital outbreaks globally. These findings underscore the considerable concern of MDR and hypervirulent K. pneumoniae in Peruvian hospitals. These findings emphasize the pressing need for sustained genomic surveillance, enhanced infection control measures, and strategies to address the expanding problem of MDR K. pneumoniae.

1 June 2014 in Emerging Infectious Diseases
Verified
Journal Article
Open access
AMAarón Martin-Alonso
Aarón Martin-Alonso
MSMayday Soto
Mayday Soto
PFPilar Foronda
Pilar Foronda
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori
GBGuillermo Bonnet
Guillermo Bonnet
MQMaría A. Quispe-Ricalde
María A. Quispe-Ricalde

11 June 2018 in Journal of the European Academy of Dermatology and Venereology
Verified
Journal Article
Closed access
PDF file
Max Carlos Ramírez-SotoMax Carlos Ramírez-Soto
Max Carlos Ramírez-Soto
JAJ. Andagua‐Castro
J. Andagua‐Castro
MQMaria Antonieta Quispe
Maria Antonieta Quispe
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori

1 September 2011 in Revista Peruana de Medicina Experimental Y Salud Pública
Verified
Journal Article
Open access
PDF file
Max Carlos Ramírez-SotoMax Carlos Ramírez-Soto
Max Carlos Ramírez-Soto
JAJonathan Andagua-Castro
Jonathan Andagua-Castro
JLJosé Lizárraga-Trujillo
José Lizárraga-Trujillo
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori
JPJusto Darwin Pezo-Ochoa
Justo Darwin Pezo-Ochoa
A descriptive study was conducted between the months of May and August 2008 in Santa Teresa Medical Center, Abancay. Of 33 patients clinically suspected with Sporotrichosis: 20 patients were identified with Sporothrix schenckii. 11 (55%) of patients were males. Children between 0 and 14 years were most affected. 60% of the lesions were fixed cutaneous being more frequent in the head and neck (40%). 55% had lessions for less than one month. In pediatric population with involvement of head and neck, Sporotrichosis should be considered in the differential diagnosis of skin lesions of patients from endemic areas.

25 July 2020 in Transactions of the Royal Society of Tropical Medicine and Hygiene
Verified
Journal Article
Closed access
YAYahanda Gisela Apaza-Castillo
Yahanda Gisela Apaza-Castillo
EAElsa Gladys Aguilar Ancori
Elsa Gladys Aguilar Ancori
MQMercedes Maritza Quispe-Flórez
Mercedes Maritza Quispe-Flórez
Max Carlos Ramírez-SotoMax Carlos Ramírez-Soto
Max Carlos Ramírez-Soto
RPRosa Luz Pacheco-Venero
Rosa Luz Pacheco-Venero
Background: Cutaneous leishmaniasis (CL) is generally diagnosed by molecular methods, including PCR, using biopsy samples, skin scrapings and clinical exudates. In this study, we assessed the PCR performance for diagnosis of CL using skin of biopsy samples vs PCR of skin lesion exudate samples on filter paper and compared the diagnostic concordance of PCR using both sampling methods. Methods: We assessed the PCR performance using 80 skin biopsy samples and 80 filter paper samples containing exudates from skin lesions obtained from 74 patients with clinical suspicion of CL in Cusco, Peru. Results: : PCR using skin biopsy samples had superior diagnostic accuracy compared with filter paper PCR (62.5% [50/80] vs 38.7% [31/80], respectively; p˂0.005) and the diagnostic concordance between both sampling methods was ‘moderate’ (kappa coefficient=0.50, 95% CI 0.98 to 1.0). Conclusions: PCR using biopsy samples remains the standard for diagnosis of CL.