Summary
We present two new methods to quantify the attraction and repulsion ofParamecium aurelia by chemicals. These are a T-maze assay and a countercurrent separation assay.
In the T-maze assay, cells were placed in one arm of a three-way stopcock. The cells were then allowed to enter the other two arms, one of which contained an attractant or repellent. The ratio of cells collected from these two arms was an index of chemotaxis. The reproducibility of this method was demonstrated, using potassium acetate to study attraction (positive chemotaxis), and quinine-HCl to study repulsion (negative chemotaxis). This method is rapid and convenient.
The countercurrent separation assay was adapted from the method of Dusenbery (1973), originally used to study behavior in nematodes. Animals were injected into the center of a slanted tube through which two solutions of different densities were pumped in opposite directions. One solution contained an attractant or repellent. Animals emerging from the tube in each of the two solutions were counted. These counts were used to measure the extent of chemotaxis. This method is useful for studying attraction in populations of over 104 paramecia and for isolating mutants defective in chemotaxis.
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The authors are grateful to S.-Y. Chang and P. Foletta for their very capable technical assistance. This work was supported in part by grants from the U.S. Public Health Service and National Science Foundation to C.K.
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Van Houten, J., Hansma, H. & Kung, C. Two quantitative assays for chemotaxis inParamecium . J. Comp. Physiol. 104, 211–223 (1975). https://doi.org/10.1007/BF01379461
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DOI: https://doi.org/10.1007/BF01379461