• 제목/요약/키워드: giemsa stain

검색결과 53건 처리시간 0.024초

위점막에서 H. pylori 검출을 위한 조직염색법의 비교 (Comparative Analysis of Histochemical Stains about Detection of H. pylori in Gastric Mucosa)

  • 차민선
    • 대한임상검사과학회지
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    • 제39권3호
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    • pp.223-230
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    • 2007
  • Several methods have been used in the detection of Helicobacter pylori (H. pylori) which was believed to be a pathogenic organism causing chronic gastritis, benign peptic ulcer, gastric carcinoma or malignant lymphoma. Even though several methods were introduced for detection of H. pylori in stomach, there were controversies in their sensitivities and specificities. This experiment were designed to study the comparative analysis of staining methods (hematoxylin and eosin (H&E), Giemsa, Warthin-Starry and immunohistochemical stain) to dectect H. pylori in the gastric mucosa. The results were as follows. Average density score of H. pylori classified by Genta were 2.29 in Warthin-Starry stain, 2.19 in Giemsa stain, 1.34 in immunohistochemical stain and 0.98 in H&E stain. By comparison between inflammatory degree by Sydney system and result of Warthin-Starry stain, the detection rate and densities of H. pylori were increased from mild (61.5% and 0.8), moderate (90.4 and 2.1), and severe (100% and 3.2). From the above findings, Warthin-Starry stain is useful method for detection of H. pylori in gastric mucosa.

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Application of Giemsa stain for easy detection of Trichinella spiralis muscle larvae

  • Ramirez-Melgar, Carmen;Gomez-Priego, Alberto;De-La-Rosa, Jorge-Luis
    • Parasites, Hosts and Diseases
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    • 제45권1호
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    • pp.65-68
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    • 2007
  • The application of Giemsa technique to stain compressed diaphragm samples obtained from rodents experimentally infected with Trichinella spiralis is described. Diaphragm samples from rats heavily infected with 20 muscle larvae per gram of body weight(20 ML/gbw) were cut into several pieces and stained with Giemsa; on the other hand, whole diaphragms from slightly infected mice(1 ML/gbw) were also stained with Giemsa. Besides, muscle samples were also stained with Giemsa. Observation at 10 $\times$ magnification revealed that both ML and nurse cells(NC) look as bluish structures clearly contrasting with the pinkish color of the non-infected muscle fibers. NC in the diaphragms of mice could be easily observed at naked eye as blue points contrasting with the pink surrounding areas formed by the non-infected muscle fibers. Among NC observed in the diaphragms of rats infected with 20 ML/gbw, 4.4% was multiple infection. These findings were confirmed in sectioned and hematoxylin-eosin stained specimens. This data could be usefulness for a rapid diagnosis of trichinellosis in post-mortem mammals without magnification procedures.

크��토스포리디움증의 실험실적 진단법 (Techniques for laboratory diagnosis of cryptosporidiosis)

  • 노재욱;강두원;장두환;강영배
    • 대한수의학회지
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    • 제31권4호
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    • pp.501-507
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    • 1991
  • Diagnosis of cryptosporidiosis is currently confirmed by the detection of the oocysts or endogenous stages in fecal or tissue samples. Various conventional staining methods and serodiagnostic techniques have been reported, but the latter has far been limited to a few laboratories. Cryptosporidium has recently been reported in mice and chiekens in Korea, but there has been no report on staining methods to the oocysts. The present study was performed by light and scanning electron microscopic observations, and discussed with staining properties of four conventional methods such as dichromate solution floatation method, Carbol fuchsin stain, Auramine-O stain and Giemsa stain method. Cryptosporidial oocysts were isolated from the laboratory mouse. In tissue sections of duodenum, jejunum, ileum, cecum and upper colon, numerous very small, basophilic bodies were observed on the border of mucosal epithelial cells. In scanning electron microscopic observations, a few of developmental stages of Cryptosporidium were seen. Two types of thick and thin-walled oocysts were recognized in the intestinal contents. Mean size of its were $5.19{\pm}0.23{\times}4.31{\pm}0.32{\mu}m$ and $5.14{\pm}0.25{\times}4.27{\pm}0.4{\mu}m$, respectively. Carbol fuchsin and Auramine-O stain methods are recommended as the satisfactory ones for the identification of Cryptosporidium oocysts. Giemsa stain was also recommended as available in the laboratory, because a few of developmental stage fo Cryptosporidium could be seen by it.

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한우의 림프절내 림프구양 세포에서 Theileria sergenti schizonts의 검출 (Detection of Theileria sergenti schizonts in lymphoid cell of lymph node in Korean cattle)

  • 이승옥;이주묵;권오덕;박진호;박상열
    • 대한수의학회지
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    • 제37권1호
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    • pp.189-194
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    • 1997
  • The life cycle of Theileria sergenti(T sergenti) in cattle, especially Korean native cattle, was not proved clearly. To find schizont stage in the life cycle of T sergenti in Korean cattle, T sergenti schizonts in the cells of parotid lymph nodes from 10 adult Korean cattle were examined. Lymphoid cells which were separated from these lymph nodes were cytocentrifuged to observe the parasites in the cells. T sergenti schizonts were detected in the cells of lymph nodes of 6 cattle out of them by IFA(Indirect Fluorescent Antibody) test and Giemsa stain. By peroxidase stain, the cells which contain schizonts were proved lymphoid cells. T sergenti schizonts identified by IFA test were able to be restained by Giemsa stain. Also, merozoites were observed in peripheral blood of the same 6 cattle that had schizonts, by giemsa stain, but not observed in the 4 cattle that had not been detected schizonts. As a part of life cycle of T sergenti, schizonts were observed in the lymphoid cells of Korean cattle.

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말라리아 진단을 위한 Acridine Orange 염색법과 Giemsa 염색법의 효율성 비교 (Comparison of acridine orange and giemsa stains for malaria diagnosis)

  • 공현희;정동일
    • Parasites, Hosts and Diseases
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    • 제33권4호
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    • pp.391-394
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    • 1995
  • 말라리아의 진단 방법으로 흔히 사용되고 있는 Giemsa 염색법과 형광염색법중 Acridine orange(AO) 염색법을 비교하였다. 말라리아 환자의 혈액을 채취하여 Giemsa와 AO로 염색하여 각각 광학현미경 및 형광현미경으로 관찰하였다. AO 염색법은 Giemsa 염색법에 비해 저배율에서도 쉽게 말라리아 원충을 찾을 수 있어 빠르고 정확한 말라리아의 진단을 위해 Acridineorange 염색법이 더 효과적이라고 생각된다.

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신생 송아지에 있어서 Theileria sergenti의 감염에 관한 연구 (Study on Infection of Theileria Sergenti in Neonatal Calves)

  • 이우종;이성식;이재구;백병걸
    • 한국동물위생학회지
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    • 제17권1호
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    • pp.37-43
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    • 1994
  • The rate of 58 neonatal calves in infection of Theileria sergenti was investigated in random samples on the farms located in Kyunggi, Chonbuk districts of Korea. 1. The criteria used in veryfying infection with T. sergenti included the detection of parasites by giemsa stain and acridine orange stain in the blood smear slides. 2. Further evidence of current or previous exposure to T. sergenti was based on demonstration of T. sergenti specific antibody and antigen by the western immunoblot and the directed immunofluorescent antibody test in the peripherial blood of the calves. 3. The prevalence rates were 35%, 50% in Kyunggi, Chonbuk provinces respectively and the overall prevalence in all the farms was 43.2% by means of acridine orange stain. 4. The parasites that were observed in the peripherial blood of calves was showen surely by the western immunoblot to the characteristic 34KD antigen among the proteins of T. sergenti (Korean isolate). 5. And the antigen of the neonatal calves reacted at the very highest titer(1 : 2, 560) 6. These data highlight the significances of T. sergenti in the neonatal calf disease in Korea.

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Argyrophilic nucleolar organizer region(AgNOR) 염색을 이용한 림프구의 미세핵분석법의 개선 (Improvement of micronucleus assay in the lymphocytes using Argyrophilic nucleolor organizer region(AgNOR) staining)

  • 김성호;한동운;강문일;임정택
    • 대한수의학회지
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    • 제36권2호
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    • pp.277-281
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    • 1996
  • A technique to improve the analysis of micronuclei(MN) in lymphocytes as a cytogenetic indicator is reported. For the purpose of diminishing the variation of the result from individual reader and making it easier to distinguish accurately a cytokinesis blicked(CB) lymphocyte and micronuclei, we tried a modified one-step silver staining technique as a method for detection of the argyrophilic nucleolar organizer region(AgNOR) with or without conventional Giemsa stain in the slide from CB method. Compared with the conventional Giemsa stain, the preparation processed with this method are especially useful for the accurate analysis of MN of cultured lymphocyte with cytochalasin B. This method will be a useful technique for automated calculation of MN.

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Prevalence of Babesia spp. in dogs of Seogwipo-si, Jeju-do, South Korea

  • Oh, Seung-Tae;Woo, Ho-Choon
    • 한국동물위생학회지
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    • 제32권4호
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    • pp.377-380
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    • 2009
  • Dogs with canine babesiosis may present with wide variation in the severity of clinical signs, ranging from a hyperacute, shock-associated, hemolytic crisis to an inapparent, subclinical infection. Dogs typically present with the acute form of babesiosis, which is characterized by general findings such as pyrexia, weakness, mucous membrane pallor, depression, hemorrhagic anemia. This study was conducted to investigate the prevalence of babesia spp. infection in dogs of Seogwipo-si. A survey of canine babesia spp. infections among 173 dogs in Seogwipo-si was performed from July 2008 to August 2008. Blood samples were collected from dogs raised outdoors through cephalic or jugular vein and Babesia spp. was diagnosed by examination of blood smear stained with Giemsa stain. Of 173 dogs, 9 dogs (5.2%) were infected with the babesia spp. This result was a little lower than the prevalence of Babesia spp. in dogs of other areas.

개의 바베세아병 1예 (A case of Canine Babesiasis)

  • 서동일
    • 대한수의사회지
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    • 제13권3호
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    • pp.167-168
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    • 1977
  • A case of canine babesiasis in a about 2 years old male Retriever dog was presented. The diagnosis was comfirmed by the examination of blood smear with Giemsa stain. The patient was completly recovered with the intramuscular injection of $7{\%}$

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어류 혈액 염색에 Diff-Quick kit의 적용 가능성 검토 (Application of a Commercial Diff-Quick Kit for Fish Hematology)

  • 박성우;김동완;최민순
    • 한국어병학회지
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    • 제17권2호
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    • pp.151-157
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    • 2004
  • 수산 혈액학에 시판의 Diff-Quick kit를 사용할 수 있는지의 여부를 검토하였다. 제조사의 지시에 따라 뱀장어의 말초혈액의 도말표본을 염색하였을 때는 핵의 염색성이 불량하여 핵 내에 미염색의 부분도 남아 있고, 또한 세포질의 호염기성도 저하되었으며, 백혈구 과립의 염색도 불량하여 상법으로 사용하는 May-Glunward Giemsa염색에 비해 염색성이 나빴다. 그러나 염색 시간을 변경하여 solution I에 5초, solution II에 10초 염색 후 이온교환수로 세척하였을 때 양호한 결과를 얻었으며, 혈구의 분류도 가능한 것으로 나타났다. 이러한 염색 조건을 다른 어종인 메기를 비롯한 3종의 어류의 말초혈액의 도말표본에 적용해본 결과 이들 어류의 혈액 염색에도 적용 가능한 것으로 나타났다.