Kinetics of virus-induced hemolysis measured for single erythrocytes
Virology, ISSN: 0042-6822, Vol: 174, Issue: 2, Page: 593-598
1990
- 6Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations6
- Citation Indexes6
- CrossRef5
- Captures4
- Readers4
Article Description
Individual erythrocytes are visible in bright-field microscopy because their enclosed hemoglobin provides a high degree of contrast against a glass slide. Lysis of these cells is detected as the loss of contrast of individual cells caused by the leakage of cell contents. Using these optical properties of erythrocytes, we have developed a new technique to examine the time course of hemolysis induced by Sendai virus at neutral pH and by influenza virus at acidic pH. Viruses were allowed to aggregate erythrocytes at 4° and the temperature was raised to allow hemolysis. Influenza-induced hemolysis at low pH, as determined by this method, occurred at a faster rate than that induced by Sendai at neutral pH. As the lysis of individual cells is detected by this method, we have discerned a cooperative “cluster” effect: Once an erythrocyte within an aggregate lyses, the likelihood of lysis of another erythrocyte in that aggregate is increased.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0042682290901125; http://dx.doi.org/10.1016/0042-6822(90)90112-5; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0025191186&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/2154891; https://linkinghub.elsevier.com/retrieve/pii/0042682290901125; http://dx.doi.org/10.1016/0042-6822%2890%2990112-5; https://dx.doi.org/10.1016/0042-6822%2890%2990112-5
Elsevier BV
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