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1.
Gastroenterology and Hepatology from Bed to Bench. 2015; 8 (2): 123-131
en Inglés | IMEMR | ID: emr-178186

RESUMEN

Over the last decades, the incidence of infestation by minor parasites has decreased in developed countries. Infectious agents can also suppress autoimmune and allergic disorders. Some investigations show that various protozoa and helminthes are connected with the main immune-mediated intestinal conditions including celiac disease [CD], inflammatory bowel diseases [IBD] and irritable bowel syndrome [IBS]. Celiac disease is a digestive and autoimmune disorder that can damage the small intestine and characterized by a multitude gastrointestinal [GI] and extra GI symptoms. IBD [including ulcerative colitis and Crohn's disease] is a group of inflammatory conditions of the small intestine and colon. The etiology of IBD is unknown, but it may be related to instability in the intestinal microflora that leading to an immoderate inflammatory response to commensal microbiota. Irritable bowel syndrome [IBS] is a common, long-term condition of the digestive system. Bloating, diarrhoea and/or constipation are nonspecific symptoms of IBS. Various studies have shown that some intestinal parasites can effect on immune system of infected hosts and in some cases, they are able to modify and change the host's immune responses, particularly in autoimmune disorders like celiac disease and IBD. The main objective of this review is to investigate the relationship between intestinal parasites and different inflammatory bowel disorders


Asunto(s)
Humanos , Enfermedad Celíaca , Enfermedades Inflamatorias del Intestino , Síndrome del Colon Irritable
2.
Gastroenterology and Hepatology from Bed to Bench. 2014; 7 (2): 82-88
en Inglés | IMEMR | ID: emr-133141

RESUMEN

Hydatidosis, caused by Echinococcus granulosus is one of the most important zoonotic diseases, throughout most parts of the world. Hydatidosis is endemic in Iran and responsible for approximately 1% of admission to surgical wards. There are extensive genetic variations within E. granulosus and 10 different genotypes [G1-G10] within this parasite have been reported. Identification of strains is important for improvement of control and prevention of the disease. No new review article presented the situation of Echinococcus granulosus genotypes in Iran in the recent years; therefore in this paper we reviewed the different studies regarding Echinococcus granulosus genotypes in Iran.

3.
Gastroenterology and Hepatology from Bed to Bench. 2014; 7 (3): 168-172
en Inglés | IMEMR | ID: emr-147112

RESUMEN

The aim of this study is to investigate the molecular identification of Giardia lamblia in patients with diarrhea. Giardiasis caused by Giardia lamblia is a common intestinal disease. Although this parasitic infection found in mammals including human, pets and livestock, but few species within the genus Giardia can infects humans. G. lamblia have seven complex genotypes termed [A-H]. Genotype A and B the main causes of human infections. Sixty seven microscopically positive G. Lamblia samples were collected from clinical laboratories in Isfahan province between June 2013 and February 2014. Extraction of genomic DNA was performed for 65 concentrated cysts and 2 cultured trophozoites. Partial sequences of tpi including 148-bp and 81-bp were amplified for detection the genotypes A and B using RFLP- PCR protocol respectively. PCR results showed that out of 67 patients with giardiasis infection, genotype A [148 bp] was detected in 40 isolates [59.70%] compared to genotype B [81 bp] isolated was detected in 25 isolates [37.31%]. Also two isolates [2.98%] had mix infection infected with genotype A and B. By comparing the frequency of genotype A [81.8%] and genotype B [13.6%], we found that genotype A is six times higher prevalence than genotype B in patients with diarrhea. We suggest that using sensitive techniques and larger sample for detection of G. lamblia genotypes and their subtypes would be necessary for investigation the immune system respond and correlation with diarrhea in the future studies in Iran

4.
The Korean Journal of Parasitology ; : 413-418, 2014.
Artículo en Inglés | WPRIM | ID: wpr-70339

RESUMEN

Hydatid cyst caused by Echinococcus granulosus is one of the most important parasitic diseases around the world and many countries in Asia, including Iran, are involved with this infection. This disease can cause high mortality in humans as well as economic losses in livestock. To date, several molecular methods have been used to determine the genetic diversity of E. granulosus. So far, identification of E. granulosus using real-time PCR fluorescence-based quantitative assays has not been studied worldwide, also in Iran. Therefore, the aim of this study was to investigate the genetic diversity of E. granulosus from center of Iran using real-time PCR method. A total of 71 hydatid cysts were collected from infected sheep, goat, and cattle slaughtered in Isfahan, Iran during 2013. DNA was extracted from protoscolices and/or germinal layers from each individual cyst and used as template to amplify the mitochondrial cytochrome c oxidase subunit 1 gene (cox1) (420 bp). Five cattle isolates out of 71 isolates were sterile and excluded from further investigation. Overall, of 66 isolates, partial sequences of the cox1 gene of E. granulosus indicated the presence of genotypes G1 in 49 isolates (74.2%), G3 in 15 isolates (22.7%), and G6 in 2 isolates (3.0%) in infected intermediate hosts. Sixteen sequences of G1 genotype had microgenetic variants, and they were compared to the original sequence of cox1. However, isolates identified as G3 and G6 genotypes were completely consistent with original sequences. G1 genotype in livestock was the dominant genotype in Isfahan region, Iran.


Asunto(s)
Animales , Bovinos , Análisis por Conglomerados , ADN de Helmintos/química , Equinococosis/parasitología , Echinococcus granulosus/clasificación , Complejo IV de Transporte de Electrones/genética , Variación Genética , Genotipo , Cabras , Irán , Filogenia , Reacción en Cadena en Tiempo Real de la Polimerasa , Análisis de Secuencia de ADN , Ovinos
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