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1.
Arch Environ Contam Toxicol ; 81(2): 189-198, 2021 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-34250569

RESUMO

The aquifer flowing beneath the Yucatan Peninsula, México, is one of the largest in the world and is in direct contact with the surface through "cenotes" (sinkholes) that have been documented to be contaminated with various classes of pollutants. The objective of this study was to evaluate the environmental status of the Great Mayan Aquifer through a review of data published on pollution of the cenotes. Approximately 1000 known georeferenced cenotes on the Yucatan Peninsula were geographically located. A map was generated using the geographic information system software. High-resolution satellite images were processed to complement the "QuickMap Services" and the formatting service of the Environmental Systems Research Institute. From the literature, 173 cenotes were identified as being sampled for various pollutants, and of these, one or more classes of pollutants were detected in 160 (i.e., greater than 92%) of the cenotes. Pollutants reported to be present included bacteria and viruses of human origin, fecal sterols, polycyclic aromatic hydrocarbons (PAHs), pesticides, pharmaceuticals, illicit drugs and personal care products. From the review of the literature, only 13 cenotes were reported to be free of the target pollutants. From this study, it can be concluded that the aquifer system with the Yucatan Peninsula is vulnerable to contamination from pollutants originating from wastewater, as well as surface runoff and infiltration from urban and agricultural lands.


Assuntos
Água Subterrânea , Praguicidas , Hidrocarbonetos Policíclicos Aromáticos , Monitoramento Ambiental , Poluição Ambiental , Humanos , México , Hidrocarbonetos Policíclicos Aromáticos/análise
2.
J Environ Sci Health B ; 56(10): 877-883, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34486949

RESUMO

The objectives of this study were to examine cytotoxic and genotoxic damage in human BJ fibroblasts caused by three pesticides used worldwide by trypan blue dye exclusion assays and to measure the relative level of phosphorylated histone H2A.X by flow cytometry at different concentrations. Captan-based fungicide and methyl thiophanate-based fungicide (100 and 1000 µΜ) showed immediate cytotoxic effects; furthermore, after 24 h, captan-based fungicide, chlorothalonil-based fungicide and methyl thiophanate-based fungicide caused cytotoxic effects in the concentration ranges of 40-100 µM, 30-100 µM and 150-1000 µM, respectively. All fungicides generated DNA damage in the treated cells by activating ATM and H2A.X sensor proteins. The three fungicides tested generated DNA double-stranded breaks and showed cytotoxicity at concentrations 33, 34, and 5 times lower (captan, chlorothalonil and thiophanate-methyl respectively) than those used in the field, as recommended by the manufacturers.


Assuntos
Fungicidas Industriais , Tiofanato , Captana , Dano ao DNA , Fibroblastos , Fungicidas Industriais/toxicidade , Humanos , Nitrilas , Tiofanato/toxicidade
3.
Dent Med Probl ; 61(3): 391-399, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38963395

RESUMO

BACKGROUND: In Mexico and around the world, water in dental units, including triple syringes, comes from municipal chlorinated water mains. The microbial contamination of dental unit water systems constitutes a risk factor for opportunistic infections. OBJECTIVES: The present work aimed to identify the bacteria present in the triple-syringe water lines of dental units at a dental school of a public university in Mexico, with a hypothesis that opportunistic bacteria of importance to human health would be found. MATERIAL AND METHODS: A cross-sectional study was carried-out. A total of 100 samples of triple-syringe tubing from dental units operated by a dental school of a public university in Mexico were analyzed before and after their use in dental practice. Bacterial biofilm was cultured and isolated from the tubing, using standard microbiological methods, and then the species present were identified through 16S rRNA gene sequencing. The characterization of the biofilm was performed by means of scanning electron microscopy (SEM). RESULTS: Bacterial growth was observed in 20% of the non-disinfected and 10% of the disinfected samples, with 11 strains isolated. Six genera and 11 bacterial species were genetically identified. Coagulasenegative staphylococci (CoNS), considered opportunistic human pathogens, were among the most critical microorganisms. Scanning electron microscopy revealed a thick polymeric matrix with multiple bacterial aggregates. CONCLUSIONS: Opportunistic bacteria from human skin and mucous membranes were detected. Under normal conditions, these bacteria are incapable of causing disease, but are potentially harmful to immunosuppressed patients.


Assuntos
Biofilmes , Contaminação de Equipamentos , Seringas , Microbiologia da Água , Estudos Transversais , México , Humanos , Seringas/microbiologia , Equipamentos Odontológicos/microbiologia , Microscopia Eletrônica de Varredura , Bactérias/isolamento & purificação , Genótipo , RNA Ribossômico 16S
4.
Artigo em Inglês | MEDLINE | ID: mdl-37075338

RESUMO

Mycetoma is a neglected tropical disease (NTD) declared by the World Health Organization (WHO) in 2016. It is characterized by the progressive growth of nodules and granulomatous lesions on the legs, arms, and trunk. It is potentially disfiguring and causes disability or amputations in working-age people from marginalized areas. The causative agents can be fungi (eumycetoma) or actinobacteria (actinomycetoma), the latter being the most common in America and Asia. Nocardia brasiliensis is the most important causal agent of actinomycetoma in the Americas. Taxonomic problems have been reported when identifying this species, so this study aimed to detect the 16S rRNA gene variations in N. brasiliensis strains using an in silico enzymatic restriction technique. The study included strains from clinical cases of actinomycetoma in Mexico, isolated from humans and previously identified as N. brasiliensis by traditional methods. The strains were characterized microscopically and macroscopically, then subjected to DNA extraction and amplification of the 16S rRNA gene by PCR. The amplification products were sequenced, and consensus sequences were constructed and used for genetic identification and in silico restriction enzyme analysis with the New England BioLabs® NEBcutter program. All study strains were molecularly identified as N. brasiliensis; however, in silico restriction analysis detected a diversity in the restriction patterns that were finally grouped and subclassified into 7 ribotypes. This finding confirms the existence of subgroups within N. brasiliensis. The results support the need to consider N. brasiliensis as a complex species.


Assuntos
Micetoma , Nocardiose , Nocardia , Humanos , Micetoma/diagnóstico , Micetoma/genética , Micetoma/microbiologia , RNA Ribossômico 16S/genética , América Latina , Genes de RNAr , Nocardia/genética , Região do Caribe , Nocardiose/genética , Nocardiose/microbiologia
5.
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1431359

RESUMO

ABSTRACT Mycetoma is a neglected tropical disease (NTD) declared by the World Health Organization (WHO) in 2016. It is characterized by the progressive growth of nodules and granulomatous lesions on the legs, arms, and trunk. It is potentially disfiguring and causes disability or amputations in working-age people from marginalized areas. The causative agents can be fungi (eumycetoma) or actinobacteria (actinomycetoma), the latter being the most common in America and Asia. Nocardia brasiliensis is the most important causal agent of actinomycetoma in the Americas. Taxonomic problems have been reported when identifying this species, so this study aimed to detect the 16S rRNA gene variations in N. brasiliensis strains using an in silico enzymatic restriction technique. The study included strains from clinical cases of actinomycetoma in Mexico, isolated from humans and previously identified as N. brasiliensis by traditional methods. The strains were characterized microscopically and macroscopically, then subjected to DNA extraction and amplification of the 16S rRNA gene by PCR. The amplification products were sequenced, and consensus sequences were constructed and used for genetic identification and in silico restriction enzyme analysis with the New England BioLabs® NEBcutter program. All study strains were molecularly identified as N. brasiliensis; however, in silico restriction analysis detected a diversity in the restriction patterns that were finally grouped and subclassified into 7 ribotypes. This finding confirms the existence of subgroups within N. brasiliensis. The results support the need to consider N. brasiliensis as a complex species.

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