An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity

Bacteriophage are among the most diverse and numerous microbes inhabiting our planet. Yet many laboratory activities fail to engage students in meaningful exploration of their diversity, unique characteristics, and abundance. In this curriculum activity students use a standard plaque assay to enumer...

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Autores principales: Mary E. Allen, Ruth A. Gyure
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Lenguaje:EN
Publicado: American Society for Microbiology 2013
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Acceso en línea:https://doaj.org/article/f42b7a2cd78d4c1dba9871b940a8ec60
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spelling oai:doaj.org-article:f42b7a2cd78d4c1dba9871b940a8ec602021-11-15T15:03:51ZAn Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity10.1128/jmbe.v14i1.5341935-78851935-7877https://doaj.org/article/f42b7a2cd78d4c1dba9871b940a8ec602013-01-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/jmbe.v14i1.534https://doaj.org/toc/1935-7877https://doaj.org/toc/1935-7885Bacteriophage are among the most diverse and numerous microbes inhabiting our planet. Yet many laboratory activities fail to engage students in meaningful exploration of their diversity, unique characteristics, and abundance. In this curriculum activity students use a standard plaque assay to enumerate bacteriophage particles from a natural sample and use the scientific method to address questions about host specificity and diversity. A raw primary sewage sample is enriched for bacteriophage using hosts in the family Enterobacteriaceae. Students hypothesize about host specificity and use quantitative data (serial dilution and plaque assay) to test their hypotheses. Combined class data also help them answer questions about phage diversity. The exercise was field tested with a class of 47 students using pre- and posttests. For all learning outcomes posttest scores were higher than pretest scores at or below p = 0.01. Average individualized learning gain (G) was also calculated for each learning outcome. Students’ use of scientific language in reference to bacteriophage and host interaction significantly improved (p = 0.002; G = 0.50). Improved means of expression helped students construct better hypotheses on phage host specificity (G = 0.31, p = 0.01) and to explain the plaque assay method (G = 0.33, p = 0.002). At the end of the exercise students also demonstrated improved knowledge and understanding of phage specificity as related to phage therapy in humans (p < 0.001; G = 51).Mary E. AllenRuth A. GyureAmerican Society for MicrobiologyarticleSpecial aspects of educationLC8-6691Biology (General)QH301-705.5ENJournal of Microbiology & Biology Education, Vol 14, Iss 1, Pp 84-92 (2013)
institution DOAJ
collection DOAJ
language EN
topic Special aspects of education
LC8-6691
Biology (General)
QH301-705.5
spellingShingle Special aspects of education
LC8-6691
Biology (General)
QH301-705.5
Mary E. Allen
Ruth A. Gyure
An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
description Bacteriophage are among the most diverse and numerous microbes inhabiting our planet. Yet many laboratory activities fail to engage students in meaningful exploration of their diversity, unique characteristics, and abundance. In this curriculum activity students use a standard plaque assay to enumerate bacteriophage particles from a natural sample and use the scientific method to address questions about host specificity and diversity. A raw primary sewage sample is enriched for bacteriophage using hosts in the family Enterobacteriaceae. Students hypothesize about host specificity and use quantitative data (serial dilution and plaque assay) to test their hypotheses. Combined class data also help them answer questions about phage diversity. The exercise was field tested with a class of 47 students using pre- and posttests. For all learning outcomes posttest scores were higher than pretest scores at or below p = 0.01. Average individualized learning gain (G) was also calculated for each learning outcome. Students’ use of scientific language in reference to bacteriophage and host interaction significantly improved (p = 0.002; G = 0.50). Improved means of expression helped students construct better hypotheses on phage host specificity (G = 0.31, p = 0.01) and to explain the plaque assay method (G = 0.33, p = 0.002). At the end of the exercise students also demonstrated improved knowledge and understanding of phage specificity as related to phage therapy in humans (p < 0.001; G = 51).
format article
author Mary E. Allen
Ruth A. Gyure
author_facet Mary E. Allen
Ruth A. Gyure
author_sort Mary E. Allen
title An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
title_short An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
title_full An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
title_fullStr An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
title_full_unstemmed An Undergraduate Laboratory Activity Demonstrating Bacteriophage Specificity
title_sort undergraduate laboratory activity demonstrating bacteriophage specificity
publisher American Society for Microbiology
publishDate 2013
url https://doaj.org/article/f42b7a2cd78d4c1dba9871b940a8ec60
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