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1.
Rev. argent. microbiol ; 50(4): 359-364, Dec. 2018. ilus, tab
Artigo em Inglês | LILACS | ID: biblio-977257

RESUMO

Helicobacter pylori is a gastric pathogen that is widely recognized as a causative agent of gastric disease. Its eradication is variable, mainly due to increased resistance to clarithromycin. Our objective was: to evaluate (i) if the biopsy specimen used for the rapid urease test is a useful sample to detect resistance to clarithromycin by PCR-RFLP and (ii) the distribution of A2142G and A2143G point mutations in the 23S rRNA gene, in relation to virulence factors in our region. Gastric specimens were collected from adult dyspeptic patients (n = 141) and H. pylori was investigated by the rapid urease test, histopathological analysis and PCR for the hsp60 gene. Clarithromycin resistance was detected by PCR-RFLP in 62 H. pylori (+) paired biopsy specimens submitted to molecular analysis and the rapid urease test. H. pylori virulence factors were analyzed by multiplex PCR using specific primers for the cagA, vacA and babA2 genes. Thirteen out of 62 strains (20.9%) were resistant to clarithromycin: 6/13 (46.2%) harbored the A2143G mutation whereas 7/13 (53.8%) carried the A2142G point mutation. vacA m1s1 was the most frequent genotype among the resistant strains. In conclusion, the biopsy specimens used for the rapid urease test were suitable samples for clarithromycin resistance detection in patients infected with H. pylori, which became especially useful in cases where the number or size of the biopsies is limited. In addition, this is the first report of a molecular analysis for clarithromycin resistance performed directly from gastric biopsies in our region.


Helicobacter pylori es un patógeno ampliamente reconocido como causante de enfermedad gástrica. Su erradicación es variable, principalmente debido al incremento de la resistencia a claritromicina. Nuestros objetivos fueron evaluar la utilidad de la biopsia usada para realizar el test rápido de ureasa en la detección de resistencia a claritromicina por PCR-RFLP y conocer la distribución de las mutaciones puntuales A2142G y A2143G en el gen ARNr 23S, en relación con los factores de virulencia en nuestra región. Se recolectaron muestras gástricas (n=141) provenientes de pacientes adultos dispépticos y se investigó la presencia de H. pylori mediante el test rápido de ureasa, análisis histopatológico y PCR para el gen hsp60. La resistencia a claritromicina se analizó por PCR-RFLP en 62 muestras pareadas de biopsias gástricas H. pylori+ destinadas al análisis molecular y al test rápido de ureasa. Los factores de virulencia de H. pylori fueron analizados mediante PCR multiplex usando oligonucleótidos específicos para los genes cagA, vacA y babA2. Trece de 62 cepas (20,9%) fueron resistentes a claritromicina, 6/13 (46,2%) llevaron la mutación A2143G, mientras que 7/13 (53,8%) presentaron la mutación A2142G. El genotipo vacA s1m1 fue el más frecuente entre las cepas resistentes a claritromicina. En conclusión, las biopsias destinadas al test rápido de ureasa fueron muestras apropiadas para la detección de la resistencia a claritromicina en pacientes infectados con H. pylori. Esto es especialmente útil en aquellos casos en los que el número o el tamaño de las muestras son limitados. Además, este es el primer reporte de estudio de resistencia a claritromicina (mediante técnicas moleculares), directamente de biopsias gástricas en nuestra región.


Assuntos
Humanos , Helicobacter pylori/efeitos dos fármacos , Infecções por Helicobacter/diagnóstico , Claritromicina/farmacologia , Fatores de Tempo , Urease/metabolismo , Polimorfismo de Fragmento de Restrição , Testes de Sensibilidade Microbiana , Reação em Cadeia da Polimerase , Helicobacter pylori/enzimologia , Helicobacter pylori/genética , Helicobacter pylori/patogenicidade , Infecções por Helicobacter/microbiologia , Mutação Puntual , Farmacorresistência Bacteriana , Testes Diagnósticos de Rotina/métodos
2.
Rev Argent Microbiol ; 50(4): 359-364, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29602600

RESUMO

Helicobacter pylori is a gastric pathogen that is widely recognized as a causative agent of gastric disease. Its eradication is variable, mainly due to increased resistance to clarithromycin. Our objective was: to evaluate (i) if the biopsy specimen used for the rapid urease test is a useful sample to detect resistance to clarithromycin by PCR-RFLP and (ii) the distribution of A2142G and A2143G point mutations in the 23S rRNA gene, in relation to virulence factors in our region. Gastric specimens were collected from adult dyspeptic patients (n=141) and H. pylori was investigated by the rapid urease test, histopathological analysis and PCR for the hsp60 gene. Clarithromycin resistance was detected by PCR-RFLP in 62 H. pylori (+) paired biopsy specimens submitted to molecular analysis and the rapid urease test. H. pylori virulence factors were analyzed by multiplex PCR using specific primers for the cagA, vacA and babA2 genes. Thirteen out of 62 strains (20.9%) were resistant to clarithromycin: 6/13 (46.2%) harbored the A2143G mutation whereas 7/13 (53.8%) carried the A2142G point mutation. vacA m1s1 was the most frequent genotype among the resistant strains. In conclusion, the biopsy specimens used for the rapid urease test were suitable samples for clarithromycin resistance detection in patients infected with H. pylori, which became especially useful in cases where the number or size of the biopsies is limited. In addition, this is the first report of a molecular analysis for clarithromycin resistance performed directly from gastric biopsies in our region.


Assuntos
Claritromicina/farmacologia , Infecções por Helicobacter/diagnóstico , Helicobacter pylori/efeitos dos fármacos , Testes Diagnósticos de Rotina/métodos , Farmacorresistência Bacteriana , Infecções por Helicobacter/microbiologia , Helicobacter pylori/enzimologia , Helicobacter pylori/genética , Helicobacter pylori/patogenicidade , Humanos , Testes de Sensibilidade Microbiana , Mutação Puntual , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Fatores de Tempo , Urease/metabolismo
3.
Acta Gastroenterol Latinoam ; 43(3): 231-4, 2013 Sep.
Artigo em Espanhol | MEDLINE | ID: mdl-24303690

RESUMO

sophageal squamous papilloma is an uncommon, usually asymptomatic, benign tumor of the squamous epithelium consisting of a raised, sessile, small and round (smooth or rough) lesion. The prevalence is between 0.01 and 0.45% of cases, with a male/female ratio of 3:1. The etiology and pathogenesis appear to be a mechanical or chemical irritation of the mucosa in addition to the presence of human papillomavirus (HPV), important agent in the evolution to a squamous carcinoma, especially HPV types 16 and 18. In this paper, we describe a case of esophageal papilloma whose diagnosis involved endoscopic images, pathological studies and detection of viral DNA by polymerase chain reaction. By using molecular techniques (PCR-RFLP) a profile consistent with HPV type 16 has been obtained. The patient underwent polypectomy and currently, after 3 years of diagnosis, he remains asymptomatic. This work is one of the first national reports of a patient with esophageal papilloma in which one of the most frequently HPV genotypes associated with esophageal carcinoma (HPV 16) has been detected.


Assuntos
DNA Viral/análise , Neoplasias Esofágicas/virologia , Papillomavirus Humano 16/genética , Papiloma/virologia , Infecções por Papillomavirus/complicações , Adulto , Neoplasias Esofágicas/patologia , Papillomavirus Humano 16/isolamento & purificação , Humanos , Masculino , Papiloma/patologia , Infecções por Papillomavirus/diagnóstico , Reação em Cadeia da Polimerase
4.
Rev Argent Microbiol ; 45(1): 39-43, 2013.
Artigo em Espanhol | MEDLINE | ID: mdl-23560787

RESUMO

Our goals were: a) to detect Helicobacter pylori in gastric biopsies of symptomatic adults by PCR, b) to detect the presence of the cagA gene as well as of the allelic variants of the vacA gene, and c) to correlate genotypes with the endoscopic diagnoses. H. pylori was detected in 81 % (39/48) of patients by nested PCR for hsp60. The presence of cagA was detected in 15/22 of samples and vacA s1 - m1 was the most frequent allelic combination (15/22). Gastritis, the most frequent diagnosis, was associated with genotype cagA+ in 10/13 of patients. In this group, 9/13 showed the allelic variant vacA s1- m1. The variant vacA s2 - m2 was detected in 3/3 of gastritis cases by H. pylori with the cagA- genotype. These results are the first reported in our region and provide data of epidemiological interest.


Assuntos
Gastrite/epidemiologia , Infecções por Helicobacter/epidemiologia , Helicobacter pylori/genética , Estômago/microbiologia , Adolescente , Adulto , Idoso , Alelos , Antígenos de Bactérias/genética , Argentina/epidemiologia , Proteínas de Bactérias/genética , Biópsia , Chaperonina 60/genética , DNA Bacteriano/genética , Doenças do Esôfago/epidemiologia , Doenças do Esôfago/microbiologia , Feminino , Gastrite/microbiologia , Gastroenteropatias/epidemiologia , Gastroenteropatias/microbiologia , Gastroscopia , Frequência do Gene , Genótipo , Infecções por Helicobacter/microbiologia , Helicobacter pylori/isolamento & purificação , Helicobacter pylori/patogenicidade , Humanos , Masculino , Pessoa de Meia-Idade , Estômago/patologia , Virulência/genética , Adulto Jovem
5.
Rev. argent. microbiol ; 45(1): 39-43, mar. 2013.
Artigo em Espanhol | LILACS, BINACIS | ID: biblio-1171770

RESUMO

Our goals were: a) to detect Helicobacter pylori in gastric biopsies of symptomatic adults by PCR, b) to detect the presence of the cagA gene as well as of the allelic variants of the vacA gene, and c) to correlate genotypes with the endoscopic diagnoses. H. pylori was detected in 81


(39/48) of patients by nested PCR for hsp60. The presence of cagA was detected in 15/22 of samples and vacA s1 - m1 was the most frequent allelic combination (15/22). Gastritis, the most frequent diagnosis, was associated with genotype cagA+ in 10/13 of patients. In this group, 9/13 showed the allelic variant vacA s1- m1. The variant vacA s2 - m2 was detected in 3/3 of gastritis cases by H. pylori with the cagA- genotype. These results are the first reported in our region and provide data of epidemiological interest.


Assuntos
Estômago/microbiologia , Gastrite/epidemiologia , Helicobacter pylori/genética , Infecções por Helicobacter/epidemiologia , Adolescente , Adulto , Adulto Jovem , Alelos , Antígenos de Bactérias/genética , Argentina/epidemiologia , Biópsia , /genética , DNA Bacteriano/genética , Doenças do Esôfago/epidemiologia , Doenças do Esôfago/microbiologia , Estômago/patologia , Feminino , Frequência do Gene , Gastrite/microbiologia , Gastroenteropatias/epidemiologia , Gastroenteropatias/microbiologia , Gastroscopia , Genótipo , Helicobacter pylori/isolamento & purificação , Helicobacter pylori/patogenicidade , Humanos , Idoso , Infecções por Helicobacter/microbiologia , Masculino , Pessoa de Meia-Idade , Proteínas de Bactérias/genética , Virulência/genética
6.
Acta gastroenterol. latinoam ; 43(3): 231-4, 2013 Sep.
Artigo em Espanhol | LILACS, BINACIS | ID: biblio-1157381

RESUMO

sophageal squamous papilloma is an uncommon, usually asymptomatic, benign tumor of the squamous epithelium consisting of a raised, sessile, small and round (smooth or rough) lesion. The prevalence is between 0.01 and 0.45


of cases, with a male/female ratio of 3:1. The etiology and pathogenesis appear to be a mechanical or chemical irritation of the mucosa in addition to the presence of human papillomavirus (HPV), important agent in the evolution to a squamous carcinoma, especially HPV types 16 and 18. In this paper, we describe a case of esophageal papilloma whose diagnosis involved endoscopic images, pathological studies and detection of viral DNA by polymerase chain reaction. By using molecular techniques (PCR-RFLP) a profile consistent with HPV type 16 has been obtained. The patient underwent polypectomy and currently, after 3 years of diagnosis, he remains asymptomatic. This work is one of the first national reports of a patient with esophageal papilloma in which one of the most frequently HPV genotypes associated with esophageal carcinoma (HPV 16) has been detected.


Assuntos
DNA Viral/análise , Infecções por Papillomavirus/complicações , Neoplasias Esofágicas/virologia , /genética , Papiloma/virologia , Adulto , Humanos , Infecções por Papillomavirus/diagnóstico , Masculino , Neoplasias Esofágicas/patologia , /isolamento & purificação , Papiloma/patologia , Reação em Cadeia da Polimerase
7.
Acta Gastroenterol. Latinoam. ; 43(3): 231-4, 2013 Sep.
Artigo em Espanhol | BINACIS | ID: bin-132817

RESUMO

sophageal squamous papilloma is an uncommon, usually asymptomatic, benign tumor of the squamous epithelium consisting of a raised, sessile, small and round (smooth or rough) lesion. The prevalence is between 0.01 and 0.45


of cases, with a male/female ratio of 3:1. The etiology and pathogenesis appear to be a mechanical or chemical irritation of the mucosa in addition to the presence of human papillomavirus (HPV), important agent in the evolution to a squamous carcinoma, especially HPV types 16 and 18. In this paper, we describe a case of esophageal papilloma whose diagnosis involved endoscopic images, pathological studies and detection of viral DNA by polymerase chain reaction. By using molecular techniques (PCR-RFLP) a profile consistent with HPV type 16 has been obtained. The patient underwent polypectomy and currently, after 3 years of diagnosis, he remains asymptomatic. This work is one of the first national reports of a patient with esophageal papilloma in which one of the most frequently HPV genotypes associated with esophageal carcinoma (HPV 16) has been detected.


Assuntos
DNA Viral/análise , Neoplasias Esofágicas/virologia , Papillomavirus Humano 16/genética , Papiloma/virologia , Infecções por Papillomavirus/complicações , Adulto , Neoplasias Esofágicas/patologia , Papillomavirus Humano 16/isolamento & purificação , Humanos , Masculino , Papiloma/patologia , Infecções por Papillomavirus/diagnóstico , Reação em Cadeia da Polimerase
8.
Rev. Argent. Microbiol. ; 45(1): 39-43, 2013 Jan-Mar.
Artigo em Espanhol | BINACIS | ID: bin-133180

RESUMO

Our goals were: a) to detect Helicobacter pylori in gastric biopsies of symptomatic adults by PCR, b) to detect the presence of the cagA gene as well as of the allelic variants of the vacA gene, and c) to correlate genotypes with the endoscopic diagnoses. H. pylori was detected in 81


(39/48) of patients by nested PCR for hsp60. The presence of cagA was detected in 15/22 of samples and vacA s1 - m1 was the most frequent allelic combination (15/22). Gastritis, the most frequent diagnosis, was associated with genotype cagA+ in 10/13 of patients. In this group, 9/13 showed the allelic variant vacA s1- m1. The variant vacA s2 - m2 was detected in 3/3 of gastritis cases by H. pylori with the cagA- genotype. These results are the first reported in our region and provide data of epidemiological interest.


Assuntos
Gastrite/epidemiologia , Infecções por Helicobacter/epidemiologia , Helicobacter pylori/genética , Estômago/microbiologia , Adolescente , Adulto , Idoso , Alelos , Antígenos de Bactérias/genética , Argentina/epidemiologia , Proteínas de Bactérias/genética , Biópsia , Chaperonina 60/genética , DNA Bacteriano/genética , Doenças do Esôfago/epidemiologia , Doenças do Esôfago/microbiologia , Feminino , Gastrite/microbiologia , Gastroenteropatias/epidemiologia , Gastroenteropatias/microbiologia , Gastroscopia , Frequência do Gene , Genótipo , Infecções por Helicobacter/microbiologia , Helicobacter pylori/isolamento & purificação , Helicobacter pylori/patogenicidade , Humanos , Masculino , Pessoa de Meia-Idade , Estômago/patologia , Virulência/genética , Adulto Jovem
9.
Acta Gastroenterol Latinoam ; 41(4): 308-11, 2011 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-22292227

RESUMO

In this paper, we describe a particular clinical case of gastrointestinal Kaposi's sarcoma associated with acquired immunodeficiency syndrome in a 51-year-old female patient who survived 6 years without anti-retroviral treatment after the diagnosis of HIV infection. The patient was admitted to our hospital with fever, skin lesions in both upper limbs and thighs (one day of evolution) and dry cough (about a month of evolution). She was admitted to the General Internal Medicine Service for control, diagnosis and treatment. An upper digestive bleeding was detected there. Once referred to our Gastroenterology Service, an appropriate selection of tests (anamnesis, gastric video endoscopy, histology) was carried out. In the upper gastric video endoscopy, several epithelial lesions were observed and a presumptive diagnosis of Kaposi's sarcoma was obtained. The diagnosis was finally confirmed by chain polymerase reaction (PCR) amplifcation of HHV8 DNA. This finding highlights the contribution of the molecular biology laboratory that allowed in this case the first molecular identification in our institution of the causative agent of Kaposi's syndrome with gastrointestinal manifestations.


Assuntos
Síndrome da Imunodeficiência Adquirida/complicações , Neoplasias Gastrointestinais/etiologia , Sarcoma de Kaposi/etiologia , DNA Viral/análise , Feminino , Neoplasias Gastrointestinais/diagnóstico , Herpesvirus Humano 8/genética , Humanos , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Sarcoma de Kaposi/diagnóstico
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