You are a graduate student working to construct a single gene knockout library of Leptospiria kirschneri, one the causative agents of leptospirosis. You are looking for single gene mutants which disrupt the bacterium’s spirillum shape to determine what role this rare cellular morphology may play in disease development and progression. Using an appropriate donor strain, you introduce the plasmid shown into L. kirschneri. L. kirschneri is not able to replicate the plasmid. The repeat regions are denoted on the plasmid map as vertical black lines, the transposase is denoted as tnp, and kanamycin kinase is denoted as aph. The larger of the two regions is transposed. Following selection and counter-selection, you isolate several non-spirillum colonies, which you use to infect juvenile piglets. Most of the infected piglets develop leptospirosis. Isolating L. kirschneri from these animals reveals that it has regained its spirillum morphology. What is a likely explanation for this reversion of morphology?' A. The bacterium acquired a mutation which inactivated the transposon B. The genes regulating cellular morphology are only expressed during active infection C. The transposon excised from its original site of integration and integrated into a different position in the chromosome. D.   The transposon was lost when the plasmid failed to replicate E. The bacterium never integrated the transposon

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You are a graduate student working to construct a single gene knockout library of Leptospiria kirschneri, one the causative agents of leptospirosis. You are looking for single gene mutants which disrupt the bacterium’s spirillum shape to determine what role this rare cellular morphology may play in disease development and progression. Using an appropriate donor strain, you introduce the plasmid shown into L. kirschneriL. kirschneri is not able to replicate the plasmid. The repeat regions are denoted on the plasmid map as vertical black lines, the transposase is denoted as tnp, and kanamycin kinase is denoted as aph. The larger of the two regions is transposed. Following selection and counter-selection, you isolate several non-spirillum colonies, which you use to infect juvenile piglets. Most of the infected piglets develop leptospirosis. Isolating L. kirschneri from these animals reveals that it has regained its spirillum morphology. What is a likely explanation for this reversion of morphology?'

A. The bacterium acquired a mutation which inactivated the transposon

B. The genes regulating cellular morphology are only expressed during active infection

C. The transposon excised from its original site of integration and integrated into a different position in the chromosome.

D.   The transposon was lost when the plasmid failed to replicate

E. The bacterium never integrated the transposon

You are a graduate student working to construct a single gene knockout library of Leptospiria kirschneri, one the causative agents of leptospirosis. You are looking for single
gene mutants which disrupt the bacterium's spirillum shape to determine what role this rare cellular morphology may play in disease development and progression. Using an
appropriate donor strain, you introduce the plasmid shown into L. kirschneri. L. kirschneri is not able to replicate the plasmid. The repeat regions are denoted on the plasmid
map as vertical black lines, the transposase is denoted as tnp, and kanamycin kinase is denoted as aph. The larger of the two regions is transposed. Following selection and
counter-selection, you isolate several non-spirillum colonies, which you use to infect juvenile piglets. Most of the infected piglets develop leptospirosis. Isolating L. kirschneri
from these animals reveals that it has regained its spirillum morphology. What is a likely explanation for this reversion of morphology?
orit
oriR6k
tetAP
tnp
aph
The bacterium acquired a mutation which inactivated the transposon
The genes regulating cellular morphology are only expressed during active infection
The transposon excised from its original site of integration and integrated into a different position in the chromosome.
The transposon was lost when the plasmid failed to replicate
The bacterium never integrated the transposon
Submit Answer
Tries 0/99
Transcribed Image Text:You are a graduate student working to construct a single gene knockout library of Leptospiria kirschneri, one the causative agents of leptospirosis. You are looking for single gene mutants which disrupt the bacterium's spirillum shape to determine what role this rare cellular morphology may play in disease development and progression. Using an appropriate donor strain, you introduce the plasmid shown into L. kirschneri. L. kirschneri is not able to replicate the plasmid. The repeat regions are denoted on the plasmid map as vertical black lines, the transposase is denoted as tnp, and kanamycin kinase is denoted as aph. The larger of the two regions is transposed. Following selection and counter-selection, you isolate several non-spirillum colonies, which you use to infect juvenile piglets. Most of the infected piglets develop leptospirosis. Isolating L. kirschneri from these animals reveals that it has regained its spirillum morphology. What is a likely explanation for this reversion of morphology? orit oriR6k tetAP tnp aph The bacterium acquired a mutation which inactivated the transposon The genes regulating cellular morphology are only expressed during active infection The transposon excised from its original site of integration and integrated into a different position in the chromosome. The transposon was lost when the plasmid failed to replicate The bacterium never integrated the transposon Submit Answer Tries 0/99
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