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1.
Acta sci., Health sci ; Acta sci., Health sci;44: e56061, Jan. 14, 2022.
Article in English | LILACS | ID: biblio-1367436

ABSTRACT

The increase in the generation of Solid Urban Waste causes social, environmental problems and damages to the population's health. Professionals who work in the collection of recyclable waste are exposed to risks of contamination either by toxic elements or pathogenic organisms. The objective of the work was to estimate the types and prevalence of intestinal parasites inwaste pickers. A field research was carried out from December 2017 to April 2018 with the voluntary participation of 26 waste pickers belonging to three associations in the municipality of Conselheiro Lafaiete, Minas Gerais, Brazil (CAAE: nº 79937817.7.0000.8122). In addition to the application a socio-environmental questionnaire, each volunteer provided a stool sample for laboratory testing the parasitological examination. Of the 26 survey participants, four (15.4%) had a positive result and were infected by the parasites Giardia lamblia, Entamoebacoliand Iodamoeba butschlii. Among the main factors that can contribute to the infection these waste pickersare the ingestion of untreated water for consumption in addition to reduced access to Personal Protective Equipment(PPE) during waste management. One way to control the presence of parasites would be through health and environmental education actions, periodic parasitological examinations and permanent use of PPE.


Subject(s)
Humans , Male , Parasites/parasitology , Waste Pickers , Solid Waste Use , Environmental Pollution/prevention & control , Parasitology , Water Pollution/analysis , Health Education , Giardia lamblia/parasitology , Entamoebiasis/parasitology , Feces/parasitology , Personal Protective Equipment , Sustainable Development
2.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;50(4): e5997, 2017. graf
Article in English | LILACS | ID: biblio-839277

ABSTRACT

Amebiasis is one of the twenty major causes of disease in Mexico; however, the diagnosis is difficult due to limitations of conventional microscopy-based techniques. In this study, we analyzed stool samples using polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) to differentiate between Entamoeba histolytica (pathogenic) and E. dispar (non-pathogenic). The target for the PCR amplification was a small region (228 bp) of the adh112 gene selected to increase the sensitivity of the test. The study involved 62 stool samples that were collected from individuals with complaints of gastrointestinal discomfort. Of the 62 samples, 10 (16.1%) were positive for E. histolytica while 52 (83.9%) were negative. No sample was positive for E. dispar. These results were validated by nested PCR-RFLP (restriction fragment length polymorphism) and suggest that PCR-DGGE is a promising tool to differentiate among Entamoeba infections, contributing to determine the specific treatment for patients infected with E. histolytica, and therefore, avoiding unnecessary treatment of patients infected with the non-pathogenic E. dispar.


Subject(s)
Humans , Denaturing Gradient Gel Electrophoresis/methods , Entamoeba histolytica/genetics , Entamoeba histolytica/isolation & purification , Entamoeba/genetics , Entamoeba/isolation & purification , Polymerase Chain Reaction/methods , DNA, Protozoan/genetics , Entamoebiasis/parasitology , Polymorphism, Restriction Fragment Length , Reproducibility of Results
3.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;47(1): 101-104, Jan-Feb/2014. tab
Article in English | LILACS | ID: lil-703150

ABSTRACT

Introduction: This study evaluated the frequency of intestinal parasites, emphasizing the identification and differentiation of Entamoeba spp. Methods: Multiplex polymerase chain reaction (PCR), coproantigen tests and morphometric analysis were performed for Entamoeba spp. differentiation. Results: The overall frequency of intestinal parasites was 65%. Entamoeba histolytica was detected by the coproantigen test, and the PCR showed that Entamoeba dispar predominated in the population. In contrast, morphometric analysis was important for identifying Entamoeba hartmanni. Conclusions: It is possible to identify the causative agent of amoebiasis and to differentiate this agent from other species by combining techniques. .


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Young Adult , Entamoeba/classification , Entamoebiasis/epidemiology , Feces/parasitology , Brazil/epidemiology , DNA, Protozoan/analysis , Enzyme-Linked Immunosorbent Assay , Entamoeba/genetics , Entamoeba/immunology , Entamoebiasis/diagnosis , Entamoebiasis/parasitology , Multiplex Polymerase Chain Reaction
4.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;47(1): 52-56, Jan-Feb/2014. tab, graf
Article in English | LILACS | ID: lil-703167

ABSTRACT

Introduction: Epidemiological studies on amebiasis have been reassessed since Entamoeba histolytica and E. dispar were first recognized as distinct species. Because the morphological similarity of these species renders microscopic diagnosis unreliable, additional tools are required to discriminate between Entamoeba species. The objectives of our study were to compare microscopy with ELISA kit (IVD®) results, to diagnose E. histolytica infection, and to determine the prevalence of amebiasis in a sample of students from southeastern Brazil. Methods: In this study, diagnosis was based on microscopy due to its capacity for revealing potential cysts/trophozoites and on two commercial kits for antigen detection in stool samples. Results: For 1,403 samples collected from students aged 6 to 14 years who were living in Divinópolis, Minas Gerais, Brazil, microscopy underestimated the number of individuals infected with E. histolytica/E. dispar (5.7% prevalence) compared with the ELISA kit (IVD®)-based diagnoses (15.7% for E. histolytica/E. dispar). A comparison of the ELISA (IVD®) and light microscopy results returned a 20% sensitivity, 97% specificity, low positive predictive value, and high negative predictive value for microscopy. An ELISA kit (TechLab®) that was specific for E. histolytica detected a 3.1% (43/1403) prevalence for E. histolytica infection. Conclusions: The ELISA kit (IVD®) can be used as an alternative screening tool. The high prevalence of E. histolytica infection detected in this study warrants the implementation of actions directed toward health promotion and preventive measures. .


Subject(s)
Adolescent , Child , Female , Humans , Male , Antigens, Protozoan/analysis , Entamoebiasis/diagnosis , Feces/parasitology , Brazil/epidemiology , Cross-Sectional Studies , Enzyme-Linked Immunosorbent Assay , Entamoeba histolytica/isolation & purification , Entamoeba/isolation & purification , Entamoebiasis/epidemiology , Entamoebiasis/parasitology , Predictive Value of Tests , Reagent Kits, Diagnostic , Sensitivity and Specificity , Species Specificity
5.
Biomédica (Bogotá) ; Biomédica (Bogotá);33(1): 70-77, ene.-mar. 2013. graf, tab
Article in English | LILACS | ID: lil-675134

ABSTRACT

Introduction. Febrile neutropenia is a common complication of chemotherapy treatment of malignant hematological diseases. However, there is insufficient information regarding the infectious complications of febrile neutropenia in our country. Objective. We will evaluate the microbial characteristics of bacterial and fungal isolates and the clinical outcome of patients with febrile neutropenia who received medical attention at an oncological reference center in Colombia. Materials and methods. A prospective case series included patients with histologically confirmed oncological disease, who were admitted because of febrile neutropenia or presented with febrile neutropenia during hospitalization. Patients with benign hematological diseases were excluded. Demographic, microbiological, and clinical features as well as treatment and outcome information from patients with febrile neutropenia were obtained. We performed univariate and multivariate analyses, with mortality defined as the outcome. Results. One hundred and thirty episodes of febrile neutropenia were identified in 104 patients. The mean patient age was 19, and 53% of the patients were male. Approximately 86% of the episodes occurred in patients with hematological disorders. An infectious site was identified in 65% of patients; 41% and 24% of the febrile neutropenia pateints´ episodes exhibited a localized infectious focus and developed bloodstream infections, respectively. The majority of infections were found in blood, urine, gastrointestinal tract, and soft tissue. Distribution analysis of microbiological isolates revealed 46.4% Gram-negative bacilli, 38.4% Gram-positive cocci, 8% fungi, and 7.1% parasites; there was a 7.7% mortality rate. Appropriate empirical antimicrobial therapy was a protection-related factor in multivariate analyses (OR= 0.17; 0.034 - 0.9 95% CI; p= 0.037). Conclusions. The mortality rate was relatively low and comparable to the rate reported by developed countries. Inappropriate empirical antimicrobial therapy was the main factor associated with mortality.


Introducción. La neutropenia febril es una complicación frecuente de la quimioterapia para las neoplasias hematológicas. Se dispone de escasa información de sus complicaciones infecciosas en nuestro medio. Objetivo. Evaluar las características clínicas y microbiológicas de pacientes con neutropenia febril, así como su resultado clínico en una institución de referencia oncológica en Colombia. Materiales y métodos. Se conformó prospectivamente una serie de casos con pacientes con enfermedad oncológica confirmada, que consultaron o presentaron neutropenia febril durante la hospitalización. Se excluyeron aquellos con enfermedad hematológica benigna. Se recolectaron datos sobre variables demográficas, microbiológicas, clínicas, de tratamiento y de resultado de los pacientes. Se llevaron a cabo un análisis univariado y uno multivariado, con la mortalidad como resultado. Resultados. Se identificaron 130 episodios de neutropenia febril en 104 pacientes, con una edad media de 19 años y 53 % masculinos. El 86 % de los episodios ocurrieron en pacientes con alteraciones hematológicas. Se demostró infección en 65 % de los casos: 41 % con un foco infeccioso localizado y 27,7 % con bacteriemia. Los principales focos infecciosos se localizaron en el torrente sanguíneo, el aparato urinario, el sistema gastrointestinal, la piel y los tejidos blandos. De los aislamientos microbiológicos, 46,4 % fueron bacilos Gram negativos, 38,4 %, cocos Gram positivos, 9 %, hongos y, 7,1%, parásitos. La mortalidad global fue de 7,7 %. En el análisis multivariado la utilización de un tratamiento empírico apropiado se correlacionó con una menor mortalidad, de forma independiente (OR=0,17; IC 95% 0,034-0,9; p=0,037). Conclusiones. La tasa de mortalidad fue relativamente baja y fue comparable con lo reportado en países desarrollados. El tratamiento antimicrobiano inapropiado fue el principal factor asociado con mortalidad.


Subject(s)
Adolescent , Adult , Aged , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Young Adult , Bacterial Infections/etiology , Cancer Care Facilities , Chemotherapy-Induced Febrile Neutropenia/epidemiology , Inappropriate Prescribing/statistics & numerical data , Mycoses/etiology , Anti-Bacterial Agents/therapeutic use , Antibiotic Prophylaxis , Bacterial Infections/drug therapy , Bacterial Infections/epidemiology , Bacterial Infections/microbiology , Chemotherapy-Induced Febrile Neutropenia/complications , Colombia/epidemiology , Cross Infection/epidemiology , Cross Infection/etiology , Entamoebiasis/drug therapy , Entamoebiasis/epidemiology , Entamoebiasis/etiology , Entamoebiasis/parasitology , Hospital Mortality , Mycoses/drug therapy , Mycoses/epidemiology , Mycoses/microbiology , Neoplasms/complications , Neoplasms/drug therapy , Organ Specificity , Prospective Studies , Recurrence
6.
Exp. mol. med ; Exp. mol. med;: e15-2013.
Article in English | WPRIM | ID: wpr-165479

ABSTRACT

The parasite Entamoeba histolytica causes amebic colitis and systemic amebiasis. Among the known amebic factors contributing to pathogenesis are signaling pathways involving heterotrimeric and Ras superfamily G proteins. Here, we review the current knowledge of the roles of heterotrimeric G protein subunits, Ras, Rho and Rab GTPase families in E. histolytica pathogenesis, as well as of their downstream signaling effectors and nucleotide cycle regulators. Heterotrimeric G protein signaling likely modulates amebic motility and attachment to and killing of host cells, in part through activation of an RGS-RhoGEF (regulator of G protein signaling-Rho guanine nucleotide exchange factor) effector. Rho family GTPases, as well as RhoGEFs and Rho effectors (formins and p21-activated kinases) regulate the dynamic actin cytoskeleton of E. histolytica and associated pathogenesis-related cellular processes, such as migration, invasion, phagocytosis and evasion of the host immune response by surface receptor capping. A remarkably large family of 91 Rab GTPases has multiple roles in a complex amebic vesicular trafficking system required for phagocytosis and pinocytosis and secretion of known virulence factors, such as amebapores and cysteine proteases. Although much remains to be discovered, recent studies of G protein signaling in E. histolytica have enhanced our understanding of parasitic pathogenesis and have also highlighted possible targets for pharmacological manipulation.


Subject(s)
Animals , Humans , Entamoeba histolytica/metabolism , Entamoebiasis/parasitology , GTP-Binding Proteins/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , Signal Transduction , ras Proteins/metabolism
7.
Article in English | WPRIM | ID: wpr-103948

ABSTRACT

The present study was conducted to investigate the clinical outcomes of Entamoeba histolytica infection in symptomatic and asymptomatic Orang Asli (aborigine) communities in Malaysia. Examination was performed on 500 stool samples obtained from Orang Asli communities in 3 different states using formalin-ether concentration, trichrome staining, and single-round PCR techniques. Out of 500 stool samples, single infection of E. histolytica, Entamoeba dispar, and Entamoeba moshkovskii was identified in 3.2%, 13.4%, and 1%, respectively. In addition, 10 samples had mixed infections with E. histolytica and E. dispar. Six samples containing E. dispar were also positive for E. moshkovskii, and only 2 samples had E. histolytica in association with E. dispar and E. moshkovskii. Seventeen E. histolytica-positive samples were from symptomatic subjects, whereas the remaining 11 samples came from asymptomatic subjects. These findings suggest a predominant distribution of pathogenic potential of E. histolytica strains in this community. Therefore, further studies on genotyping of E. histolytica is required, to find out association between E. histolytica genotype and the outcome of the infection.


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Asymptomatic Diseases , Coinfection/parasitology , Entamoeba/classification , Entamoebiasis/parasitology , Feces/parasitology , Genetic Variation , Malaysia , Treatment Outcome
8.
Rev. méd. Chile ; 140(4): 476-483, abr. 2012. ilus
Article in Spanish | LILACS | ID: lil-643217

ABSTRACT

Background: Entamoeba histolytica and Entamoeba dispar are morphologically identical. However, the former is highly pathogenic and the latter is not. Aim: To differentiate Entamoeba histolytica from Entamoeba dispar through ELISA and PCR techniques in Colombian isolates from feces. Material and Methods: Descriptive study of Colombian fecal samples from 53 males and 47 women, that were positive for the complex E. histolytica/E. dispar on light microscopy. Positive samples were cultured on Robinson medium to isolate trophozoites. The presence of specific Gal/ GalNAc-lectin was determined by ELISA and polymerase chain reaction in genomic DNA, using the combination of three nucleotides that recognize a variable region of 16S small subunit ribosomal RNA, generating a 166 base pair (bp) product for E. histolytica and 752 pb product for E. dispar. Results: After verification, only eight of the 100 samples were positive for the complex E. histolytica/E. dispar and were cultivated. Isolates were obtained in six cultures, one corresponded to E. histolytica and six to E. dispar. Conclusions: The presence of E. histolytica/E. dispar complex was largely overestimated with light microscopy. In the few samples where isolates were obtained, the technique described differentiated between both strains.


Subject(s)
Female , Humans , Male , Entamoeba/metabolism , Entamoebiasis/parasitology , Colombia , DNA, Protozoan/genetics , Entamoeba histolytica/genetics , Entamoeba histolytica/isolation & purification , Entamoeba/genetics , Entamoeba/isolation & purification , Entamoebiasis/diagnosis , Enzyme-Linked Immunosorbent Assay , Feces/parasitology , Lectins , Polymerase Chain Reaction/methods , Protozoan Proteins , /genetics , Sensitivity and Specificity
10.
Braz. j. infect. dis ; Braz. j. infect. dis;15(2): 119-125, Mar.-Apr. 2011. ilus, tab
Article in English | LILACS | ID: lil-582413

ABSTRACT

Amoebiasis is an infection caused by Entamoeba histolytica and is a potential health risk in countries in which health barriers are inappropriate. Since the discovery of Entamoeba dispar, the prevalence of amoebiasis has been modified. OBJECTIVE: This study has standardized the PCR technique applied for the diagnosis of different species of the E. histolytica/E. dispar complex and has evaluated the prevalence of infection among patients attending private and public clinical laboratories in Salvador City, Bahia State, Brazil. RESULTS: Analysis of 52,704 stool samples by microscopic examination demonstrated that 1,788 (3.4 percent) were positive for the E. histolytica/E. dispar complex and infection occurred more often in samples originated from public clinical laboratories (5.0 percent) than those that came from private laboratories (3.2 percent). PCR performed in approximately 15 percent (262) E. histolytica/E. dispar complex positive samples, randomly chosen, amplified 227 samples (86.6 percent), all of them positive for E. dispar. The non-amplified 35 samples (13.4 percent) were also negative for E. histolytica-specific galactose adhesin. Moreover, to exclude a probable infection caused by E. hartmanni, morphometric analysis demonstrated that non-amplified samples had cyst sizes comparable to E. histolytica/E. dispar (>10 µm). CONCLUSION: The absence of amplification of these samples indicates the presence of PCR inhibitors in the stool samples or the presence of DNA from Entamoeba species other than E. dispar, E. histolytica or E. hartmanni.


Subject(s)
Humans , Entamoeba/genetics , Entamoebiasis/diagnosis , Entamoebiasis/parasitology , Polymerase Chain Reaction/methods , Brazil/epidemiology , Diagnosis, Differential , DNA, Protozoan/analysis , Entamoeba histolytica/genetics , Entamoeba histolytica/isolation & purification , Entamoeba/classification , Entamoeba/isolation & purification , Entamoebiasis/epidemiology , Feces/parasitology , Prevalence , Sensitivity and Specificity
11.
Cad. saúde pública ; Cad. Saúde Pública (Online);25(1): 151-159, jan. 2009. ilus, tab
Article in Spanish | LILACS | ID: lil-505618

ABSTRACT

Differential identification of Entamoeba histolytica and Entamoeba dispar is essential for both appropriate patient treatment and epidemiological purposes. To determine the prevalence of these amoeba infections in Santa Rosa de Agua (Maracaibo, Zulia State, Venezuela), a PCR assay using specific primers for each species was standardized and applied. 204 stool samples were analyzed through direct microscopic examination with SSF (0.85 percent) and lugol, formol-ether concentration, and PCR. Under direct microscopy, 42 individuals (20.58 percent) presented the E. histolytica/E. dispar complex. Meanwhile PCR showed 47 positive cases for these amoebas: 22 E. histolytica (10.78 percent), 16 E. dispar (7.84 percent), and 9 (4.41 percent) mixed infections. There was no significant difference in the presence of E. histolytica and/or E. dispar according to either gender or age. There were no cases of these amoebas in children under 2 years of age. Observed frequency of E. histolytica (31/204) shows the endemic nature of amoeba infection in this community.


La identificación diferencial de Entamoeba histolytica y Entamoeba dispar es esencial para un tratamiento adecuado del paciente y con fines epidemiológicos. Para determinar la prevalencia de E. histolytica y E. dispar se estandarizó y aplicó un ensayo de PCR, utilizando oligonucleótidos específicos para cada especie. 204 muestras de heces de individuos de la comunidad de Santa Rosa de Agua (Municipio Maracaibo, Estado Zulia, Venezuela), fueron analizadas a través del examen directo con SSF (0,85 por ciento) y lugol, concentrado de formol-éter y PCR. Al examen microscópico, 42 individuos (20,58 por ciento) presentaron formas evolutivas del complejo E. histolytica/E. dispar; mientras que la técnica de PCR evidenció un total de 47 casos positivos a estas amibas; de los cuales 22 eran portadores de E. histolytica (10,78 por ciento), 16 (7,84 por ciento) de E. dispar y 9 (4,41 por ciento) presentaron infección mixta. No hubo diferencia significativa al relacionar las variables sexo y presencia de E. histolytica y/o E. dispar, ni con los grupos etarios. No existieron casos de estas amibas, en los menores de 2 años. La frecuencia observada de E. histolytica (31/204), demuestra el carácter endémico de la amibiasis en esta comunidad.


Subject(s)
Adolescent , Adult , Aged , Animals , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , Young Adult , DNA, Protozoan/classification , Entamoeba/genetics , Entamoebiasis/diagnosis , DNA, Protozoan/isolation & purification , Entamoeba histolytica/classification , Entamoeba histolytica/genetics , Entamoeba histolytica/isolation & purification , Entamoeba/classification , Entamoeba/isolation & purification , Entamoebiasis/epidemiology , Entamoebiasis/parasitology , Feces/parasitology , Polymerase Chain Reaction , Sensitivity and Specificity , Venezuela/epidemiology , Young Adult
12.
Braz. j. infect. dis ; Braz. j. infect. dis;11(3): 365-370, June 2007. ilus
Article in English | LILACS | ID: lil-457639

ABSTRACT

Amebiasis is an infection caused by Entamoeba histolytica. However, differentiation between E. histolytica and Entamoeba dispar, which are morphologically identical species, is essential for treatment decision, precaution of the invasive disease and public health. The purpose of the present study was to evaluate a Multiplex -PCR for detection and differentiation of E. histolytica from E. dispar from fresh stool samples in comparison with the coproantigen commercial ELISA. Microscopic examination of stools using the Coprotest method, detection of stool antigen by enzyme-linked immunosorbent assay kit and a home made Multiplex-PCR, were used for the diagnosis of amoebiasis infection. Analysis of the 127 stools samples by microscopy examination demonstrated that only 27 (21 percent) samples were positive for E. histolytica/E. dispar complex. Among these stool samples, 11 were positive by Multiplex-PCR, with nine presenting the diagnostic fragment characteristic of E. dispar (96 bp) and two presenting diagnostic fragment of E. histolytica (132 bp). Among negative samples detected by microscopic examination, three positive samples for E. dispar and one positive for E. histolytica by Multiplex-PCR was observed. This denotes a low sensibility of microscopic examination when a single stool sample is analyzed. Assay for detection of E. histolytica antigen was concordant with multiplex-PCR in relation to E. histolytica. Statistical analysis comparing the sensibility tests was not done because of the low number of E. histolytica cases. The results demonstrate the importance of the specific techniques use for the differentiation between E. histolytica and E. dispar.


Subject(s)
Animals , Humans , DNA, Protozoan/analysis , Entamoeba histolytica/genetics , Entamoebiasis/diagnosis , Feces/parasitology , Polymerase Chain Reaction/methods , Antigens, Protozoan/analysis , Diagnosis, Differential , DNA, Protozoan/genetics , Entamoeba histolytica/immunology , Entamoeba histolytica/isolation & purification , Entamoeba/genetics , Entamoeba/immunology , Entamoeba/isolation & purification , Entamoebiasis/parasitology , Immunoenzyme Techniques , Reproducibility of Results , Sensitivity and Specificity
13.
Mem. Inst. Oswaldo Cruz ; 101(supl.2): 53-56, Dec. 2006. tab
Article in English | LILACS | ID: lil-441343

ABSTRACT

During the excavations of the XIX century Meadowlark cemetery (Manhattan, Kansas, US), samples of sediments were taken from around five skeletons, and analyzed to detect intestinal parasites. No helminth eggs were found, but immunological ELISA tests for Entamoeba histolytica were positive in three samples. The immunological techniques have been successfully used in paleoparasitology to detect protozoan infections. Amoebiasis could have been a severe disease in the past, especially where poor sanitary conditions prevailed, and there is evidence that this cemetery may have been used in a situation where poor sanitary conditions may have prevailed. The presence of this protozoan in US during the late XIX century gives information on the health of the population and provides additional data on the parasite's evolution since its appearance in the New World.


Subject(s)
Animals , History, 19th Century , Humans , Entamoeba histolytica/isolation & purification , Entamoebiasis/history , Mortuary Practice , Burial , Enzyme-Linked Immunosorbent Assay , Entamoebiasis/parasitology , Kansas , Paleopathology
14.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;39(4): 388-389, jul.-ago. 2006.
Article in Portuguese | LILACS | ID: lil-439886

ABSTRACT

Este trabalho teve como objetivo determinar a ocorrência das espécies Entamoeba histolytica/Entamoeba dispar em amostras clínicas de pacientes ambulatoriais de Pernambuco. Neste estudo, foi utilizado o teste imunoenzimático específico para Entamoeba histolytica, que entre os 213 pacientes não identificou nenhuma amostra fecal positiva. Estes resultados confirmam Entamoeba dispar é a espécie dominante nesta região.


The objective this study was to determine the occurrence of the species Entamoeba histolytica/Entamoeba díspar in clinical samples of ambulatory patients in Pernambuco. A specific assay for Entamoeba histolytica was used in this study, which identified no positive fecal samples among the 213 patients. These results confirm that E. dispar is the dominant species in Pernambuco State.


Subject(s)
Humans , Animals , Entamoeba/isolation & purification , Entamoebiasis/diagnosis , Brazil/epidemiology , Enzyme-Linked Immunosorbent Assay , Entamoeba histolytica/classification , Entamoeba histolytica/immunology , Entamoeba histolytica/isolation & purification , Entamoeba/classification , Entamoeba/immunology , Entamoebiasis/epidemiology , Entamoebiasis/parasitology , Feces/parasitology
15.
Braz. j. infect. dis ; Braz. j. infect. dis;6(2): 97-99, Apr. 2002.
Article in English | LILACS, SES-SP | ID: lil-332303

ABSTRACT

We describe the pathology of a unique case of Fallopian tube amebiasis, associated with hydrosalpinx, in a 21-year-old woman. She complained of lower abdominal pain, had a foul-smelling green vaginal discharge and fever during one week. There was a discrete increase in body temperature and a painful abdominal palpation at the lower right side, with signs of local peritoneal irritation. Pathological examination showed a marked dilatation of the fallopian tube and hydrosalpinx. Microscopic examination showed a poorly formed granuloma composed of large macrophages with many Entamoeba histolytica trophozoites inside the fallopian tube. Even though it is a rare disease the correct diagnosis of female genital tract amebiasis is of great importance for the indication of proper therapy.


Subject(s)
Adult , Animals , Female , Humans , Salpingitis , Entamoeba histolytica , Entamoebiasis/diagnosis , Entamoebiasis/parasitology , Salpingitis , Fallopian Tubes , Entamoebiasis/surgery
16.
Article in English | IMSEAR | ID: sea-64754

ABSTRACT

Pathogenic and non-pathogenic Entamoeba have been separated into two distinct species. Recently, the non-pathogenic E. dispar has been cultivated axenically. However, the genetic variability among different clones from the same strain, experimental production of hybrid clones which may differ from their parents, and the possibility of invasiveness of E. dispar, are some phenomena which may indicate that the last word on distinctiveness of the species has not yet been said.


Subject(s)
Animals , Cloning, Organism , Entamoeba/classification , Entamoeba histolytica/genetics , Entamoebiasis/parasitology , Genes, Protozoan , Genetic Variation , Humans , Virulence
19.
Rev. Soc. Bras. Med. Trop ; Rev. Soc. Bras. Med. Trop;28(4): 379-87, Oct.-Dec. 1995. tab, ilus
Article in Portuguese | LILACS | ID: lil-187129

ABSTRACT

Entamoeba gingivalis is found only in its trophozoite form and it is postulated that its main transmission mechanism is through the kiss. E. gingivalis is considered pathogenic by some authors and commensal to others. It does not have a defined role in the installation of disease. To address some of this questions we studied a 100 patients who were seen through the Odontological Hospital from the Universidade Federal de Uberlândia in order to determine its frequency in the buccal cavity. The material were collected using swabs from four different buccal sites and the smears were stained by a modified Papanicolaou technique. The results revealed positivity index of 62 per cent. The affinity of the dye to the food vacuole contents and to the ingested bacterias prevents clear visualisation of the central and peripherical chromatin constituents of the parasite's nucleus. Mouth washes with 3ml of saline from 10 patients, were used to evaluate which parasitological method of diagnosis (fresh, iron-haematoxylin stained, Giemsa and Papanicolaou) gives better visualisation of the parasite. The mouth washes sediment from fresh material revealed 100 per cent of positivity and clear visualisation of the free form and locomotion of the trophozoites. No stained technique of the smear showed adequate visualisation, presenting the nucleus partially covered by the food vacuoles. In stained preparations by toluidine blue ultrastructure analysis of the morphology of parasite can be observed.


Subject(s)
Humans , Animals , Male , Female , Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Periodontal Diseases/diagnosis , Entamoebiasis/diagnosis , Entamoeba/cytology , Brazil/epidemiology , Chi-Square Distribution , Periodontal Diseases/epidemiology , Periodontal Diseases/parasitology , Entamoebiasis/epidemiology , Entamoebiasis/parasitology , Entamoeba/isolation & purification , Incidence , Microscopy, Electron
20.
Indian J Exp Biol ; 1990 Apr; 28(4): 376-7
Article in English | IMSEAR | ID: sea-60510

ABSTRACT

Three isolates of E. histolytica isolated and maintained in modified Boeck and Drbohlav's medium and the axenic nonpathogenic strain NIH-200 maintained in Diamond's TPS-1 medium were used to assess the effect of histamine added to the cultures on their pathogenicity in just weaned rats of Charles Foster strain. Initially when the three polyxenic isolates were examined for their Pathogenicity after growing them with graded concentrations of histamine viz. M-2 through M-6 (log dilutions of the molar concentration of histamine dihydrochloride) the caecal scores were significantly enhanced in cultures grown with M-2 and M-3 concentrations. Subsequently NIH-200 strain was examined similarly after growing it with 20 micrograms/ml of histamine dihydrochloride through three generations. The Neal's caecal score of NIH-200 increased significantly stepwise up to second subculture and became stabilised at third generation with histamine.


Subject(s)
Amebiasis/parasitology , Animals , Entamoeba histolytica/pathogenicity , Entamoebiasis/parasitology , Histamine/pharmacology , Rats , Virulence
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