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MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii...
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| Zeitschriftentitel: | mSphere |
|---|---|
| Personen und Körperschaften: | , |
| In: | mSphere, 4, 2019, 1 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
American Society for Microbiology
|
| Schlagwörter: |
| author_facet |
Adams, Felise G. Brown, Melissa H. Adams, Felise G. Brown, Melissa H. |
|---|---|
| author |
Adams, Felise G. Brown, Melissa H. |
| spellingShingle |
Adams, Felise G. Brown, Melissa H. mSphere MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family Molecular Biology Microbiology |
| author_sort |
adams, felise g. |
| spelling |
Adams, Felise G. Brown, Melissa H. 2379-5042 American Society for Microbiology Molecular Biology Microbiology http://dx.doi.org/10.1128/mspheredirect.00028-19 <jats:p> One of the most important weapons in the armory of <jats:italic>Acinetobacter</jats:italic> is its impressive genetic plasticity, facilitating rapid genetic mutations and rearrangements as well as integration of foreign determinants carried by mobile genetic elements. Of these, IS are considered one of the key forces shaping bacterial genomes and ultimately evolution. We report the identification of a novel nonautonomous IS-derived element present in multiple bacterial species from the <jats:italic>Moraxellaceae</jats:italic> family and its recent translocation into the <jats:italic>hns</jats:italic> locus in the <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> ATCC 17978 genome. The latter finding adds new knowledge to only a limited number of documented examples of MITEs in the literature and underscores the plastic nature of the <jats:italic>hns</jats:italic> locus in <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> . MITE <jats:italic> <jats:sub>Aba12</jats:sub> </jats:italic> , and its predicted parent(s), may be a source of substantial adaptive evolution within environmental and clinically relevant bacterial pathogens and, thus, have broad implications for niche-specific adaptation. </jats:p> MITE <i> <sub>Aba12</sub> </i> , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in <i>Acinetobacter baumannii</i> ATCC 17978 and Its Prevalence across the <i>Moraxellaceae</i> Family mSphere |
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American Society for Microbiology, 2019 |
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| title |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_unstemmed |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_full |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_fullStr |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_full_unstemmed |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_short |
MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_sort |
mite
<i>
<sub>aba12</sub>
</i>
, a novel mobile miniature inverted-repeat transposable element identified in
<i>acinetobacter baumannii</i>
atcc 17978 and its prevalence across the
<i>moraxellaceae</i>
family |
| topic |
Molecular Biology Microbiology |
| url |
http://dx.doi.org/10.1128/mspheredirect.00028-19 |
| publishDate |
2019 |
| physical |
|
| description |
<jats:p>
One of the most important weapons in the armory of
<jats:italic>Acinetobacter</jats:italic>
is its impressive genetic plasticity, facilitating rapid genetic mutations and rearrangements as well as integration of foreign determinants carried by mobile genetic elements. Of these, IS are considered one of the key forces shaping bacterial genomes and ultimately evolution. We report the identification of a novel nonautonomous IS-derived element present in multiple bacterial species from the
<jats:italic>Moraxellaceae</jats:italic>
family and its recent translocation into the
<jats:italic>hns</jats:italic>
locus in the
<jats:named-content content-type="genus-species">A. baumannii</jats:named-content>
ATCC 17978 genome. The latter finding adds new knowledge to only a limited number of documented examples of MITEs in the literature and underscores the plastic nature of the
<jats:italic>hns</jats:italic>
locus in
<jats:named-content content-type="genus-species">A. baumannii</jats:named-content>
. MITE
<jats:italic>
<jats:sub>Aba12</jats:sub>
</jats:italic>
, and its predicted parent(s), may be a source of substantial adaptive evolution within environmental and clinically relevant bacterial pathogens and, thus, have broad implications for niche-specific adaptation.
</jats:p> |
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| author | Adams, Felise G., Brown, Melissa H. |
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| author_sort | adams, felise g. |
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| description | <jats:p> One of the most important weapons in the armory of <jats:italic>Acinetobacter</jats:italic> is its impressive genetic plasticity, facilitating rapid genetic mutations and rearrangements as well as integration of foreign determinants carried by mobile genetic elements. Of these, IS are considered one of the key forces shaping bacterial genomes and ultimately evolution. We report the identification of a novel nonautonomous IS-derived element present in multiple bacterial species from the <jats:italic>Moraxellaceae</jats:italic> family and its recent translocation into the <jats:italic>hns</jats:italic> locus in the <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> ATCC 17978 genome. The latter finding adds new knowledge to only a limited number of documented examples of MITEs in the literature and underscores the plastic nature of the <jats:italic>hns</jats:italic> locus in <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> . MITE <jats:italic> <jats:sub>Aba12</jats:sub> </jats:italic> , and its predicted parent(s), may be a source of substantial adaptive evolution within environmental and clinically relevant bacterial pathogens and, thus, have broad implications for niche-specific adaptation. </jats:p> |
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| spelling | Adams, Felise G. Brown, Melissa H. 2379-5042 American Society for Microbiology Molecular Biology Microbiology http://dx.doi.org/10.1128/mspheredirect.00028-19 <jats:p> One of the most important weapons in the armory of <jats:italic>Acinetobacter</jats:italic> is its impressive genetic plasticity, facilitating rapid genetic mutations and rearrangements as well as integration of foreign determinants carried by mobile genetic elements. Of these, IS are considered one of the key forces shaping bacterial genomes and ultimately evolution. We report the identification of a novel nonautonomous IS-derived element present in multiple bacterial species from the <jats:italic>Moraxellaceae</jats:italic> family and its recent translocation into the <jats:italic>hns</jats:italic> locus in the <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> ATCC 17978 genome. The latter finding adds new knowledge to only a limited number of documented examples of MITEs in the literature and underscores the plastic nature of the <jats:italic>hns</jats:italic> locus in <jats:named-content content-type="genus-species">A. baumannii</jats:named-content> . MITE <jats:italic> <jats:sub>Aba12</jats:sub> </jats:italic> , and its predicted parent(s), may be a source of substantial adaptive evolution within environmental and clinically relevant bacterial pathogens and, thus, have broad implications for niche-specific adaptation. </jats:p> MITE <i> <sub>Aba12</sub> </i> , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in <i>Acinetobacter baumannii</i> ATCC 17978 and Its Prevalence across the <i>Moraxellaceae</i> Family mSphere |
| spellingShingle | Adams, Felise G., Brown, Melissa H., mSphere, MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family, Molecular Biology, Microbiology |
| title | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_full | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_fullStr | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_full_unstemmed | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_short | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| title_sort | mite <i> <sub>aba12</sub> </i> , a novel mobile miniature inverted-repeat transposable element identified in <i>acinetobacter baumannii</i> atcc 17978 and its prevalence across the <i>moraxellaceae</i> family |
| title_unstemmed | MITE Aba12 , a Novel Mobile Miniature Inverted-Repeat Transposable Element Identified in Acinetobacter baumannii ATCC 17978 and Its Prevalence across the Moraxellaceae Family |
| topic | Molecular Biology, Microbiology |
| url | http://dx.doi.org/10.1128/mspheredirect.00028-19 |