• 제목/요약/키워드: Infectivity

검색결과 268건 처리시간 0.025초

염소에 의한 bacteriophage f2의 살균작용 (Inactivation of Bacteriophage f2 with Chlorine)

  • Chi Kyung KIM;Kyung Hee MIN
    • 미생물학회지
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    • 제16권2호
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    • pp.62-70
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    • 1978
  • Chlorine was used for inactivation of bacteriophage f2 at pH 5.5, 7.5, and 10.0 at $10^{\circ}C$. The inactivation rate phage with chlorine varied depending on the pH value and reaction time. Hypochlorous acid appeared to be the major species of free chlorine for the inactivation. Suevival of the phage treated with chlorine and infectivity of the RNA extracted from the chlorinated phage were examined. The RNA extracted from untreatd phage was chlorinated and its infectivity was assayed. All three samples showed similar rates of inactivation at pH 5.5 and 7.5, but the naked RNA was more susceptible to chlorine at pH 10.0. The rate of inactivation was compared naked RNA was more susceptible to chlorine at pH 10.0. The rate of inactivation was compared with specific and non-specific attachment of the phasge f2. The specific attachment of the phage increased after the phage had been inactivated by extended chlorination. Chlorine may penetrate to the becteriophage f2 by altering the structural integrity of the protein coat, but the main target of free chlorine for inactivation of the phage appeared to be the phage RNA.

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Resistance of Cryptosporidium parvum oocysts following commercial bleach treatment

  • Surl, Chan-gu;Jung, Bae-Dong;Park, Bae-Keun;Kim, Hyeon-cheol
    • 대한수의학회지
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    • 제51권2호
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    • pp.101-105
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    • 2011
  • We investigate the resistance of Cryptosporidium (C.) parvum oocysts to commercial bleach treatment. The viability and infectivity of C. parvum oocysts suspended in 100, 50, 25, 12.5, 6.3 or 3.2% aqueous commercial bleach for 10, 30, 60, 120 or 180 min at room temperature were assessed by nucleic acid Syto-9 staining, histologic examination of ileum and infectivity to immunosuppressed neonatal C57BL/6N mice. Although the viability was decreased compared with normal oocysts, all oocysts in contact with serially diluted commercial bleach for 180 min were alive by nucleic acid dye Syto-9 staining. And, microscopic examination of ileum sections revealed developmental stages of C. parvum in all mice. The oocyst shedding patterns between mice infected with oocysts contacted with commercial bleach and normal control mice were not significantly different each other. Although commercial bleach is widely used as a bacterial and viral disinfectant, the present findings indicate that it is not an effective disinfectant for C. parvum oocysts under practical conditions. Authors conclude that, therefore, it is undesirable to recommend commercial bleach as a disinfectant for C. parvum oocysts.

Viability of preserved Cryptosporidium baileyi oocysts

  • Surl, Chan-Gu;Kim, Se-Min;Kim, Hyeon-Cheol
    • Parasites, Hosts and Diseases
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    • 제41권4호
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    • pp.197-201
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    • 2003
  • The present study was undertaken to determine the viability and infectivity of oocysts of Cryptosporidium baileyi that had been stored from 1 to 40 months at $4^{\circ}C$ preserved in 2.5% potassium dichromate solution. Oocysts of C. baileyi were purified from the feces of experimentally infected chickens using discontinuous sucrose gradients. Subsequently, the purified oocysts were suspended in 2.5% potassium dichromate solution at a concentration of $1{\;}{\times}10^7$ organism/ml, and their viabilities were assessed by nucleic acid staining, histologic examination, and infectivity to 2-day-old chickens. All chickens inoculated with oocysts that had been stored for 1-18 months developed patent infections, while chickens infected with older oocysts remained uninfected. Between 5.8% and 82.2% of the oocysts, stored at $4^{\circ}C$ in 2.5% potassium dichromate solution, were found to be viable, as determined by nucleic acid staining. Parasite colonization in the bursa of Fabricius was detected in the microvillus border of bursal epithelium. The finding that C. baileyi oocysts remain infective to chickens for at least 18 months offers important time-saving advantages to investigators who frequently require large numbers of oocysts.

Loss of infectivity of Neospora caninum oocysts maintained for a prolonged time

  • Uzeda, Rosangela Soares;Costa, Kattyanne De Souza;Santos, Sara Lima;Pinheiro, Alexandre Moraes;Almeida, Maria Angela Ornelas De;McAllister, Milton M.;Gondim, Luis Fernando Pita
    • Parasites, Hosts and Diseases
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    • 제45권4호
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    • pp.295-299
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    • 2007
  • The purpose of this study was to investigate whether sporulated Neospora caninum oocysts, which had been stored for 46 mo in a 2% sulfuric acid solution at $4^{\circ}C$, remain morphologically viable and infective to gerbils (Meriones unguiculatus). Six gerbils were orally inoculated with doses of 400 or 1,200 oocysts. Two mo after inoculation, the animals did not show any clinical signs, had no histological lesions, and were seronegative for N. caninum at 1:50 in an immunofluorescent antibody test. PCR using the brain from each gerbil did not reveal N. caninum specific DNA. We conclude that oocysts preserved for 46 mo are not infective, despite being morphologically intact.

Infection of marine diatom Coscinodiscus wailesii(Bacillariophyceae) by the parasitic nanoflagellate Pirsonia diadema(Stramenopiles) from Yongho Bay in Korea

  • Yoo, Jiae;Kim, Sunju
    • 환경생물
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    • 제38권4호
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    • pp.567-577
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    • 2020
  • The infection of marine diatom Coscinodiscus wailesii by a parasitic protist from the Yongho Bay of Busan, Korea was observed during the diatom bloom events in 2017 through 2018. The morphological and molecular features suggested that the parasitic nanoflagellate Pirsonia diadema was responsible for the infection. During the study period, the parasite prevalence ranged from 0.3% to 3.3%, and infected C. wailesii cells were observed only at surface seawater temperatures ranging between 10.9 and 19.9℃, although the host population appeared at temperatures above 25℃. The parasite and host system was successfully established as cultures. Using the cultures, we determined the morphological features over the infection cycle, parasite generation time, parasite prevalence as a function of inoculum size, and zoospore infectivity and survival time. The diatom C. wailesii was readily infected by the parasite P. diadema, with a parasite prevalence reaching up to 100% and a zoospore to host inoculum ratio above 20:1. The survival and infectivity of the parasite zoospores decreased with age. While the zoospores could survive up to 88 hours, they quickly lost their ability to infect after 48 hours. These results could lead to a better understanding of the biology and ecology of the parasitoid infecting the giant-sized diatoms in coastal waters.

뇌염(腦炎)바이러스의 적혈구응집력가(赤血球凝集力價)와 보체결합력가(補體結合力價) 및 감염력(感染力)에 관한 연구(硏究) (Studies on the Haemagglutinating and Complement Fixing Activities, and Infectivity of Murray Valley Encephalitis Virus)

  • 정영석
    • 대한수의학회지
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    • 제12권1호
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    • pp.77-84
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    • 1972
  • 이 실험(實驗)은 뇌염(腦炎)바이러스(MVE virus)들 acetone, Tween-ether 그리고 Tween-ether-protamine-sulphate 로 처리한 후 그 바이러스가 지니고 있는 적혈구응집력가(赤血球凝集力價), 보체결합력가(補體結合力價) 그리고 감염력가(感染力價)의 변화 여부를 관찰함과 아울러 초원심분리법(超遠心分離法)에 의하여 이 바이러스가 지니고 있는 위의 세 가지 활성물질(活性物質)의 분획(分劃) 가능성(可能性)을 검토한 결과 다음과 같은 결과를 얻었다. 1) Acetone, Tween-ether 그리고 Tween-ether protamine-sulphate 처리에 의하여 MVE virus가 지니는 적혈구응집력가(赤血球凝集力價)는 8~16 배(倍)로 증가 하였다. 2) Acetone 및 Tween-ether 처리로 보체결합력가(補體結合力價)는 4 배(倍)로 증가 되었으나 Tween-ether protamine-sulphate 처리로는 저하되는 경향이 있었다. 3) Tween-ether로 처리하면 감염력가(感染力價)는 완전히 상실 되나 acetone으로 처리하면 $TCID50/log_{10}$ 3이 감퇴 되었다. 4) 위의 화학제의 처리와 관계없이 바이러스의 적혈구응집력가(赤血球凝集力價)는 $37^{\circ}C$ 에서 10 분간 가열(加熱)됨으로써 완전 소실 되었으나 보체결합력가(補體結合力價)는 상승 하였으며 이 활성도(活性度)는 $65^{\circ}C$ 에서 20 분간 까지도 계속 유지되었다. 5) 처리되지 않은 바이러스와 acetone 처리된 바이러스의 보체결합력가(補體結合力價)나 적혈구응집력가(赤血球凝集力價)는 Tween-ether 나 Tween-ether-protamine-sulphate 로 처리한 바이러스의 그것보다 열(熱)에 대해서 더 안정(安定)하였다. 6) 적혈구응집억제반응용(赤血球凝集抑制反應用) 항원제조(抗原製造)에 있어서 Tween-ether 로 처리하거나 acetone 으로 처리하여 만든 두가지 항원(抗原)은 모두 동일(同一)한 역가(力價)를 보였다. 7) 10~60%의 sucrose gradient centrifugation 에서 처리되지 않은 바이러스는 두개의 보체결합(補體結合)피크가 저농도(低濃渡)와 고농도(高濃渡)에서 각각 나타났으며 저농도(低濃渡)에서 얻은 재료는 적혈구응집력(赤血球凝集力)과 감염력(感染力)을 동반하고 있었다. 8) Acetone 으로 처리된 바이러스의 초원심분리(超遠心分離)에서는 위에 말한 두 보체결합(補體結合)피크 중 고농도부(高濃渡部)의 것은 감소 되었으나 다른 하나는 영향을 받지 않았다. 그리고 적혈구응집력가(赤血球凝集力價)가 증가된 반면 감염최고력가(感染最高力價)는 감퇴 되었으며 이 세 가지 활성(活性)은 acetone 처리 후에는 명확히 분획(分劃)되지 않았다. Tween-ether 로 처리된 바이러스는 초원심분리(超遠心分離)에 의하여 고농도부(高濃渡部)에 있는 보체결합(補體結合)피크는 완전 소실된 반면 저농도부(低濃渡部)에 있는 보체결합최고력가(補體結合最高力價)는 영향을 받지 아니 하였으며 이 피크는 감염력(感染力)을 동반하지 않는 적혈구응집소(赤血球凝集素)와 분획(分劃)이 가능 하였다.

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A New Cancer Cell Detection Method Using an Infectivity-enhanced Adenoviral Vector

  • Uchino, Junji;Takayama, Koichi;Nakagaki, Noriaki;Shuo, Wang;Hisasue, Junko;Nakatom, Keita;Ohta, Keiichi;Hirano, Ryosuke;Tashiro, Naoki;Miiru, Izumi;Fujita, Masaki;Watanabe, Kentaro;Nakanishi, Yoichi
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권11호
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    • pp.5551-5556
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    • 2012
  • Cytological examination is widely used as a diagnostic tool because of the ease of collecting cells from the involved area. However, the diagnostic yield of cytological examination is unsatisfactory; the reasons include sampling error, poorly prepared samples, small numbers of malignant cells, and low grades of cellular atypia. In this study, we focused on the high infectivity of adenovirus towards epithelial cells and applied the luciferase-expressing adenoviral vector to a new cancer cell detection tool. In addition, adenoviral infectivity was enhanced by modifying viral fiber proteins. The sensitivity of the diagnostic tool was tested using the NCI-H1299 lung cancer cell line, and validated in body fluid samples from cancer patients with a variety of etiology. Results showed that the adenovirus efficiently transfected NCI-H1299 with high sensitivity. Only 10 cancer cells were sufficient for detection of luciferase signals. In body fluid samples, the adenovirus confirmed the diagnosis for malignant and benign cancer, but not in non-epithelial cell derived samples. This study provides proof-of-concept for a more reliable and sensitive diagnostic tool for epithelium-derived cancer.

다양한 소독제에 의한 감염성 크립토스포리디움 불활성화율 평가 (Inactivation of Infectious Cryptosporidium parvum by Various Disinfectants)

  • 변승헌;이목영;조은주;윤태호;김태호;한선희
    • 대한환경공학회지
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    • 제29권5호
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    • pp.533-539
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    • 2007
  • 본 연구에서는 염소, 오존, UV에 의한 크립토스포리디움의 불활성화정도를 평가하기 위해 HCT-8세포를 사용하는 세포배양법과 최적확수기법을 결합하였다. 이 방법은 크립토스포리디움 감염성을 평가하는데 있어 "gold standard"라고 여겨지는 동물감염성 실험 만큼이나 민감하였고 소독제에 의한 크립토스포리디움의 불활성화를 측정할 수 있는 유용한 방법이었다. 실험실규모의 연구결과, $5^{\circ}C$, pH 7.0 조건에서 크립토스포리움을 약 1 log 불활성화시키기위한 염소와 오존 CT값은 각각 $1,250mg{\cdot}min/L,\;16mg{\cdot}min/L$ 이었다. 이는 오존을 사용하여 소독하였을 때 조차도 낮은 온도에서는 크립토스포리디움을 불활성화시키기 어렵다는 것을 보여주는 것이다. 염소와 오존과는 달리 UV는 온도에 상관없이 크립토스포리디움을 불활성화시키기에 매우 효과적이어서 UV가 2 $mJ/cm^2$ 조사되었을 때 크립토스포리디움이 3 log 이상 불활성화되었다.