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1.
Cytokine ; 177: 156559, 2024 05.
Article in English | MEDLINE | ID: mdl-38412767

ABSTRACT

Over the years, there has been progress in understanding the molecular aspects of iron metabolism and erythropoiesis. However, despite research conducted both in laboratories and living organisms, there are still unanswered questions due to the complex nature of these fields. In this study we investigated the effects of hookworm infection on iron metabolism and how the hosts response to anemia is affected using hamsters infected with Ancylostoma ceylanicum as a model. Our data revealed interesting relationships between infection-induced anemia, erythropoiesis, iron metabolism, and immune modulation, such that the elevated production of erythropoietin (EPO) in renal tissue indicated intensified erythropoiesis in response to anemia. Additionally, the increased expression of the erythroferrone (ERFE) gene in the spleen suggested its involvement in iron regulation and erythropoiesis. Gene expression patterns of genes related to iron metabolism varied in different tissues, indicating tissue-specific adaptations to hypoxia. The modulation of pro-inflammatory and anti-inflammatory cytokines highlighted the delicate balance between immune response and erythropoiesis. Data derived from the investigation of changes induced in iron metabolism and stress erythropoiesis following anemia aid in our understanding of mechanisms related to blood spoliation and anemia, which could potentially be extrapolated or compared to other types or causes of anemia. These findings also contribute to our understanding of the pathophysiology of erythropoiesis in the context of blood loss.


Subject(s)
Anemia , Erythropoietin , Hookworm Infections , Humans , Erythropoiesis/physiology , Hepcidins/genetics , Anemia/etiology , Iron , Erythropoietin/metabolism , Hookworm Infections/complications
2.
PLoS One ; 14(10): e0224108, 2019.
Article in English | MEDLINE | ID: mdl-31622428

ABSTRACT

The main control strategy for Ascaris lumbricoides is mass drug administration (especially with benzimidazoles), which can select strains of parasites resistant to treatment. Mutations in the beta-tubulin isotype-1 gene at codons 167, 198 and 200 have been linked to benzimidazole resistance in several nematodes. The mutation in codon 200 is the most frequent in different species of parasites, as previously observed in Necator americanus and Trichuris trichiura; however, this mutation has never been found in populations of A. lumbricoides. This study aimed to screen for single nucleotide polymorphisms (SNPs) in the beta-tubulin isotype-1 gene at codon 200 in A. lumbricoides. We developed a technique based on an amplification refractory mutation system (ARMS-PCR) for the analysis of 854 single A. lumbricoides eggs collected from 68 human stool samples from seven Brazilian states. We detected the mutation in codon 200 at a frequency of 0.5% (4/854). This is the first report of this mutation in A. lumbricoides. Although the observed frequency is low, its presence indicates that these parasite populations have the potential to develop high levels of resistance in the future. The methodology proposed here provides a powerful tool to screen for the emergence of anthelmintic resistance mutations in parasitic nematode populations.


Subject(s)
Anthelmintics/pharmacology , Ascaris lumbricoides/drug effects , Benzimidazoles/pharmacology , Drug Resistance/genetics , Helminth Proteins/genetics , Tubulin/genetics , Animals , Anthelmintics/therapeutic use , Ascariasis/drug therapy , Ascariasis/parasitology , Ascaris lumbricoides/genetics , Ascaris lumbricoides/isolation & purification , Benzimidazoles/therapeutic use , Feces/parasitology , Genotype , Humans , Ovum/metabolism , Polymorphism, Single Nucleotide
3.
Mol Biochem Parasitol ; 232: 111200, 2019 09.
Article in English | MEDLINE | ID: mdl-31306675

ABSTRACT

Obesity and ancylostomiasis are considered public health problems. Recent studies have shown that infection by intestinal helminths in obese individuals can ameliorate metabolic disorder and improve glucose tolerance by decreasing both insulin resistance and low-intensity inflammation. However, few helminth species have been studied in this context, and some modulation mechanisms still require deeper investigation. Therefore, the present work aimed to investigate the role of experimental infection with Ancylostoma ceylanicum in the modulation of the immune response in an obese experimental model. Four groups of hamsters were used as follows: two groups were submitted to a hyperlipidic and hypercaloric diet capable of inducing obesity, one infected and the other uninfected; and two normonourished control groups, one infected and one uninfected by A. ceylanicum. Biochemical, haematological, parasitological and immunological parameters were evaluated. The results demonstrated that A. ceylanicum infection accentuated weight loss in obese animals compared to normonourished animals. However, obesity reduced the recovery of worms and oviposition of the females, and both infected groups showed decreased levels of haemoglobin, albumin, iron and erythrocytes. Significant relations were observed for pathogenesis in the following cases: infection interfered in lipid metabolism, which increased levels of total cholesterol and triglycerides in the obese group, and caused a decrease in HDL levels in both groups. Obesity led to an increase in glucose levels, and the infection exacerbated this parameter in both the normonourished and obese groups. Inflammation was intensified in obese animals that showed elevated macrophage and neutrophil activation in adipose tissue, enlargement of the spleen and accumulation of lipids in the liver and faeces. Despite the decrease in IFN-γ levels, the infection did not potentiated the expression of the Foxp3, IL-10 and IL-2 transcription factor for any of the infected groups, markers that could positively compensate the host from the damage caused by obesity.


Subject(s)
Ancylostoma/physiology , Ancylostomiasis/parasitology , Obesity/parasitology , Ancylostomiasis/genetics , Ancylostomiasis/metabolism , Animals , Cholesterol/metabolism , Cricetinae , Female , Glucose/metabolism , Humans , Interleukin-10/genetics , Interleukin-10/metabolism , Interleukin-12/genetics , Interleukin-12/metabolism , Liver/metabolism , Liver/parasitology , Male , Obesity/genetics , Obesity/metabolism , Oviposition , Triglycerides/metabolism
4.
Parasitol Res ; 118(3): 837-849, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30697644

ABSTRACT

Mass drug administration has been implicated as the major cause of drug resistance in nematodes of ruminants. Single-nucleotide polymorphisms (SNPs) at codons 167, 198, and 200 of the beta-tubulin isotype 1 gene are associated with albendazole resistance mechanisms. Although drug resistance is suspected to occur in nematodes of the same order, at present, there is no evidence of a strong correlation between these canonical SNPs and albendazole resistance in hookworms. In the absence of a hookworm strain that is naturally resistant to albendazole, we produced an albendazole-resistant Ancylostoma ceylanicum strain by selective drug pressure. Restriction fragment length polymorphism-PCR (RFLP-PCR) was employed to identify the presence of SNPs previously associated with drug resistance in other nematodes. However, none of the benzimidazole resistance-associated SNPs known in other nematodes were found. A beta-tubulin isotype 1 gene mini-cDNA library was constructed to obtain the complete cDNA gene sequence for the analysis of the entire gene to identify distinct SNPs associated with resistance. Some SNPs were found, but the resulting sequences were not reproducibly detected among the different clones, preventing their association with the resistance mechanism. The parasitological and hematological parameters of the albendazole-resistant strain were characterized and compared to those of the sensitive strain. Although the albendazole-resistant strain was less adapted to its host, with fewer worms recovered, all other parameters analyzed were similar between both strains. The results of the present study indicate that the mechanism of albendazole resistance of the resistant strain described herein must differ from those that have previously been characterized. Thus, new mechanistic studies are needed in the future.


Subject(s)
Albendazole/pharmacology , Ancylostoma/drug effects , Ancylostoma/genetics , Anthelmintics/pharmacology , Drug Resistance/genetics , Ancylostomiasis/drug therapy , Ancylostomiasis/parasitology , Animals , Benzimidazoles/pharmacology , Cricetinae , Female , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Polymorphism, Single Nucleotide/genetics , Tubulin/genetics
5.
Haueisen, Alice Luzia Miranda; Faria, Aloisio Celso Gomes de; Gomes, Ana Clara da Cunha; Costa, Ariádne Lara Gomes; Peixoto, Beatriz Mendanha; Versiani, Camila Azevedo; Dall'Aqua, Camila Gomes; Roquette, Carolina Eloá Miranda; Marques, Carolina Marveis; Lanna, Cristina Costa Duarte; Dias, Diego Alonso; Soares, Eliane Cristina de Souza; Pedroso, Ênio Roberto Pietra; Parreiras, Fernanda Cardoso; Freire, Fernanda Dias; Nunes, Fernando Emílio Pereira; Fernandes, Géssica Antonia; Lages, Gustavo Rodrigues Costa; Cruz, Helen Nayara; Oliveira, Henrique Arenare de; Inácio, Igor Lima Carence; Quadros, Isabela Antonini Alves Oliveira; Yamacita, Juliana Sayuri; Figueiredo, Juliano Alves; Porto, Julinely Gonçalves Weber; Ribeiro, Laura Defensor; Drumond, Laiane Candiotto; Reis, Letícia Pontes; Teixeira, Lucas Cezar; Xavier, Lucas da Mata; Saraiva, Lucas de Andrade; Reis, Luísa Diniz; Campos, Luísa Lazarino de Souza; Batista, Luísa Menezes; Alves, Luiz Fernando; Torres, Maíra Soares; Barbosa, Maira Tonidandel; Oliveira, Maraísa Andrade de; Starling, Marcelo Andrade; Lima, Maria Clara Resende; Simões, Mariana Figueiredo; Pires, Mariana Martins; Oliveira, Mauricio Vitor Machado; Siqueira, Natália Alves; Magalhães, Natália Caroline Teixeira; Eisenberg, Paulo Camilo de Oliveira; Pôrto, Patrícia Jacundino; Carmo, Raíssa Diniz do; Gomez, Renato Santiago; Souza, Ressala Castro; Vilela, Rodrigo Vasconcellos; Araújo, Sabrina Letícia Oliveira; Mello, Sérgio Silva de; Takahashi, Tamires Yumi; Carvalho, Thomas Mendes; Ulhoa, Thomaz Santos; Campos, Júlio Vinícius de Oliveira; Alves, William Pereira; Sasso, Yara Isis Deise Barros.
São Paulo; Perse; 2019. 271 p.
Monography in Portuguese | Coleciona SUS, BDENF - Nursing, LILACS | ID: biblio-1118186

ABSTRACT

O estudo da dor e suas particularidades é de grande importância para o tratamento de diversas patologias e para a melhora na qualidade de vida dos pacientes. A maioria das disfunções orgânicas tem a dor como um ponto importante da sua manifestação. Dessa maneira, é justificável a elaboração de conteúdo para auxiliar os profissionais da saúde no entendimento e tratamento das principais causas de dores agudas e crônicas. Este livro foi elaborado com o objetivo de servir como um guia prático para o manejo da dor por profissionais e acadêmicos de Medicina. Engloba temas como conceitos e aspectos biopsicossociais da dor, além de questões mais complexas como a fisiologia da dor e o tratamento medicamentoso com o arsenal terapêutico existente. Finalmente, também trata dos diversos tipos de dor mais prevalentes e o conhecimento básico que envolve seu manejo.


Subject(s)
Humans , Male , Female , Pregnancy , Child, Preschool , Adult , Aged , Young Adult , Pain/history , Pain/psychology , Pain, Postoperative , Physical Examination , Quality of Life , Pain Measurement/psychology , Complementary Therapies , Aged , Nociceptors , Fibromyalgia , Child , Pelvic Pain , Labor Pain , Drug Therapy , Pain Perception/physiology , Acute Pain , Musculoskeletal Pain , Chronic Pain , Cancer Pain , Headache , Analgesia , Medical History Taking
6.
Vet Parasitol ; 224: 65-67, 2016 Jul 15.
Article in English | MEDLINE | ID: mdl-27270392

ABSTRACT

The tetraprimer ARMS-PCR technique is efficient for SNP detection and can be used to search for polymorphisms associated with drug resistance. However, the establishment of this methodology is not always straightforward because of the constraints on primer design due to the restrictions of the polymorphic regions. Here, we describe the standardization of the tetraprimer ARMS-PCR methodology for the detection of a SNP at codon 198 of the Ancylostoma caninum ß-tubulin gene. This SNP is associated with resistance to albendazole in various nematodes. The methodology was used to screen 327 individuals from 6 different locations. No mutation was found in any of the samples. This methodology will be useful for screening for the E198A SNP in the ß-tubulin gene of canine hookworms in a broader population to determine whether this SNP is associated with benzimidazole resistance in this species. The method could also be adapted for the analysis of other SNPs in other nematode species.


Subject(s)
Dog Diseases/parasitology , Drug Resistance/genetics , Hookworm Infections/veterinary , Parasitology/methods , Polymerase Chain Reaction/veterinary , Tubulin/genetics , Albendazole/pharmacology , Ancylostoma/genetics , Ancylostomatoidea/drug effects , Ancylostomatoidea/genetics , Animals , Anthelmintics/pharmacology , Brazil , DNA Primers/genetics , DNA Primers/standards , Dogs , Hookworm Infections/parasitology , Polymerase Chain Reaction/standards , Polymorphism, Single Nucleotide/genetics
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