Juan Manuel Bello-López

Dr. Juan Manuel Bello-López

Hospital Juárez de México, Mexico City, Ciudad de México, Mexico
orcid
Researcher in Medical Sciences "E"

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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18 September 2019 in Microorganisms
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Juan Manuel Bello-LópezJuan Manuel Bello-López
Juan Manuel Bello-López
OCOmar A. Cabrero-Martínez
Omar A. Cabrero-Martínez
GIGabriela Ibáñez-Cervantes
Gabriela Ibáñez-Cervantes
CCCecilia Hernández Cortez
Cecilia Hernández Cortez
LPLeda I. Pelcastre-Rodríguez
Leda I. Pelcastre-Rodríguez
GRACIELA CASTRO-ESCARPULLIGRACIELA CASTRO-ESCARPULLI
GRACIELA CASTRO-ESCARPULLI
The evolution of multidrug resistant bacteria to the most diverse antimicrobials known so far pose a serious problem to global public health. Currently, microorganisms that develop resistant phenotypes to multiple drugs are associated with high morbidity and mortality. This resistance is encoded by a group of genes termed ‘bacterial resistome’, divided in intrinsic and extrinsic resistome. The first one refers to the resistance displayed on an organism without previous exposure to an antibiotic not involving horizontal genetic transfer, and it can be acquired via mutations. The latter, on the contrary, is acquired exclusively via horizontal genetic transfer involving mobile genetic elements that constitute the ‘bacterial mobilome’. This transfer is mediated by three different mechanisms: transduction, transformation, and conjugation. Recently, a problem of public health due to implications in the emergence of multi-drug resistance in Aeromonas spp. strains in water environments has been described. This is derived from the genetic material transfer via conjugation events. This is important, since bacteria that have acquired antibiotic resistance in natural environments can cause infections derived from their ingestion or direct contact with open wounds or mucosal tissue, which in turn, by their resistant nature, makes their eradication complex. Implications of the emergence of resistance in Aeromonas spp. by horizontal gene transfer on public health are discussed.

31 January 2021 in The Journal of Infection in Developing Countries
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EDEmilio Mariano Durán-Manuel
Emilio Mariano Durán-Manuel
CCClemente Cruz-Cruz
Clemente Cruz-Cruz
GIGabriela Ibáñez-Cervantes
Gabriela Ibáñez-Cervantes
JBJuan Carlos Bravata-Alcantará
Juan Carlos Bravata-Alcantará
OSOscar Sosa-Hernández
Oscar Sosa-Hernández
Juan Manuel Bello-LópezJuan Manuel Bello-López
Juan Manuel Bello-López
Introduction: SARS-CoV2 pandemic marks the need to pay attention to bacterial pathogens that can complicate the hospital stay of patients in the intensive care unit (ICU). ESKAPE bacteria which includes Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter cloacae are considered the most important, because of their close relationship with the development of ventilator-associated pneumonia (VAP). The aim of this work was to identify and characterize ESKAPE bacteria and to detect their possible clonal spread in medical devices, patients, and medical personnel of the ICU for COVID-19 patients of the Hospital Juarez de Mexico. Methodology: Genetic identification of ESKAPE bacteria was performed by analyzing the 16S rRNA gene. Resistance assays were performed according to the CLSI guidelines. Assembly of AdeABCRS operon and inhibition assays of pumps efflux in Acinetobacter baumannii isolates were performed. Associated gene involved in biofilm formation (icaA) was performed in isolates belonging to the Staphylococcus genus. Finally, typing by ERIC-PCR and characterization of mobile genetic element SCCmec were done. Results: Heterogeneous distribution of ESKAPE and non-ESKAPE bacteria was detected in various medical devices, patients, and medical personnel. Acinetobacter baumannii and Staphylococcus aureus were the predominant ESKAPE members. The analysis of intergenic regions revealed an important clonal distribution of A. baumannii (AdeABCRS+). Genotyping of SCCmec mobile genetic elements and the icaA gene showed that there is no clonal distribution of S. aureus. Conclusions: Clonal spread of A. baumannii (AdeABCRS+) highlights the importance of adopting good practices for equipment disinfection, surfaces and management of COVID-19 patients.

1 September 2020 in American Journal of Infection Control
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GIGabriela Ibáñez-Cervantes
Gabriela Ibáñez-Cervantes
JBJuan Carlos Bravata-Alcantara
Juan Carlos Bravata-Alcantara
ANAlan Steve Nájera-Cortés
Alan Steve Nájera-Cortés
SMSergio Meneses-Cruz
Sergio Meneses-Cruz
LDLaura Delgado-Balbuena
Laura Delgado-Balbuena
Juan Manuel Bello-LópezJuan Manuel Bello-López
Juan Manuel Bello-López

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Luis Uriel Gonzalez-AvilaLuis Uriel Gonzalez-Avila
Luis Uriel Gonzalez-Avila
Miguel LoyolaMiguel Loyola
Miguel Loyola
CCCecilia Hernández Cortez
Cecilia Hernández Cortez
Juan Manuel Bello-LópezJuan Manuel Bello-López
Juan Manuel Bello-López
GRACIELA CASTRO-ESCARPULLIGRACIELA CASTRO-ESCARPULLI
GRACIELA CASTRO-ESCARPULLI
The increase in the use of antimicrobials such as colistin for the treatment of infectious diseases has led to the appearance of Aeromonas strains resistant to this drug. However, resistance to colistin not only occurs in the clinical area but has also been determined in Aeromonas isolates from the environment or animals, which has been determined by the detection of mcr genes that confer a resistance mechanism to colistin. The variants mcr-1, mcr-3, and mcr-5 have been detected in the genus Aeromonas in animal, environmental, and human fluids samples. In this article, an overview of the resistance to colistin in Aeromonas is shown, as well as the generalities of this molecule and the recommended methods to determine colistin resistance to be used in some of the genus Aeromonas.

22 May 2023 in Pathogens
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Miguel LoyolaMiguel Loyola
Miguel Loyola
Luis Uriel Gonzalez-AvilaLuis Uriel Gonzalez-Avila
Luis Uriel Gonzalez-Avila
Arturo Martínez-TrejoArturo Martínez-Trejo
Arturo Martínez-Trejo
Andres Saldaña-PadillaAndres Saldaña-Padilla
Andres Saldaña-Padilla
CCCecilia Hernández Cortez
Cecilia Hernández Cortez
GRACIELA CASTRO-ESCARPULLIGRACIELA CASTRO-ESCARPULLI
GRACIELA CASTRO-ESCARPULLI
The ESKAPE group constitute a threat to public health, since these microorganisms are associated with severe infections in hospitals and have a direct relationship with high mortality rates. The presence of these bacteria in hospitals had a direct impact on the incidence of healthcare-associated coinfections in the SARS-CoV-2 pandemic. In recent years, these pathogens have shown resistance to multiple antibiotic families. The presence of high-risk clones within this group of bacteria contributes to the spread of resistance mechanisms worldwide. In the pandemic, these pathogens were implicated in coinfections in severely ill COVID-19 patients. The aim of this review is to describe the main microorganisms of the ESKAPE group involved in coinfections in COVID-19 patients, addressing mainly antimicrobial resistance mechanisms, epidemiology, and high-risk clones.

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Arturo Martínez-TrejoArturo Martínez-Trejo
Arturo Martínez-Trejo
JRJuan Manuel Ruiz-Ruiz
Juan Manuel Ruiz-Ruiz
Luis Uriel Gonzalez-AvilaLuis Uriel Gonzalez-Avila
Luis Uriel Gonzalez-Avila
Andres Saldaña-PadillaAndres Saldaña-Padilla
Andres Saldaña-Padilla
CCCecilia Hernández Cortez
Cecilia Hernández Cortez
GRACIELA CASTRO-ESCARPULLIGRACIELA CASTRO-ESCARPULLI
GRACIELA CASTRO-ESCARPULLI
Acinetobacter baumannii is a Gram-negative bacillus that causes multiple infections that can become severe, mainly in hospitalized patients. Its high ability to persist on abiotic surfaces and to resist stressors, together with its high genomic plasticity, make it a remarkable pathogen. Currently, the isolation of strains with high antimicrobial resistance profiles has gained relevance, which complicates patient treatment and prognosis. This resistance capacity is generated by various mechanisms, including the modification of the target site where antimicrobial action is directed. This mechanism is mainly generated by genetic mutations and contributes to resistance against a wide variety of antimicrobials, such as β-lactams, macrolides, fluoroquinolones, aminoglycosides, among others, including polymyxin resistance, which includes colistin, a rescue antimicrobial used in the treatment of multidrug-resistant strains of A. baumannii and other Gram-negative bacteria. Therefore, the aim of this review is to provide a detailed and up-to-date description of antimicrobial resistance mediated by the target site modification in A. baumannii, as well as to detail the therapeutic options available to fight infections caused by this bacterium.