Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>

<p>Abstract</p> <p>Background</p> <p><it>Anaplasma phagocytophilum </it>strains often vary in Msp2 expression, a situation assumed to be related to immune evasion. However, Msp2 is also an adhesin, and little is known about the role of endogenous <it>m...

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Main Authors: Ogata Hiroyuki, Caspersen Karen, Scorpio Diana G, Park Jinho, Dumler J Stephen
Format: Article
Language:English
Published: BMC 2004-01-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/4/1
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spelling doaj-99ea1050fecb4edfa654fbb5e86b58482020-11-25T02:26:02ZengBMCBMC Microbiology1471-21802004-01-0141110.1186/1471-2180-4-1Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>Ogata HiroyukiCaspersen KarenScorpio Diana GPark JinhoDumler J Stephen<p>Abstract</p> <p>Background</p> <p><it>Anaplasma phagocytophilum </it>strains often vary in Msp2 expression, a situation assumed to be related to immune evasion. However, Msp2 is also an adhesin, and little is known about the role of endogenous <it>msp2 </it>transcriptional changes in the absence of immune selection. Thus, Msp2 profiles and <it>msp2 </it>transcripts of low passage <it>A. phagocytophilum </it>Webster strain, initially comprised of a single abundant <it>msp2 </it>transcript, were re-examined after ≥ 20 in vitro passages without immune selection.</p> <p>Results</p> <p>Using an Msp2 monoclonal antibody, immunoblots revealed an unchanged dominant band and several weak bands that appeared with passage. Similarly, <it>msp2 </it>transcript diversity changed, with a decrease in the initially abundant low passage transcript and appearance of a newly abundant and several minor <it>msp2 </it>transcripts with high passage. BLASTN search of the <it>A. phagocytophilum </it>HZ strain genome revealed ≥ 52 <it>msp2 </it>paralogs.</p> <p>Conclusions</p> <p>Msp2 expression and <it>msp2 </it>transcription modulate even without immune selective pressures. However, the limited diversity of <it>msp2 </it>transcripts in the absence of immune pressure suggests selection for Msp2 by specific functions beyond that of immune evasion, in spite of a large genomic reservoir for Msp2 diversity.</p> http://www.biomedcentral.com/1471-2180/4/1
collection DOAJ
language English
format Article
sources DOAJ
author Ogata Hiroyuki
Caspersen Karen
Scorpio Diana G
Park Jinho
Dumler J Stephen
spellingShingle Ogata Hiroyuki
Caspersen Karen
Scorpio Diana G
Park Jinho
Dumler J Stephen
Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
BMC Microbiology
author_facet Ogata Hiroyuki
Caspersen Karen
Scorpio Diana G
Park Jinho
Dumler J Stephen
author_sort Ogata Hiroyuki
title Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
title_short Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
title_full Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
title_fullStr Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
title_full_unstemmed Restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>Anaplasma phagocytophilum</it>
title_sort restricted changes in major surface protein-2 (<it>msp2</it>) transcription after prolonged in vitro passage of <it>anaplasma phagocytophilum</it>
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2004-01-01
description <p>Abstract</p> <p>Background</p> <p><it>Anaplasma phagocytophilum </it>strains often vary in Msp2 expression, a situation assumed to be related to immune evasion. However, Msp2 is also an adhesin, and little is known about the role of endogenous <it>msp2 </it>transcriptional changes in the absence of immune selection. Thus, Msp2 profiles and <it>msp2 </it>transcripts of low passage <it>A. phagocytophilum </it>Webster strain, initially comprised of a single abundant <it>msp2 </it>transcript, were re-examined after ≥ 20 in vitro passages without immune selection.</p> <p>Results</p> <p>Using an Msp2 monoclonal antibody, immunoblots revealed an unchanged dominant band and several weak bands that appeared with passage. Similarly, <it>msp2 </it>transcript diversity changed, with a decrease in the initially abundant low passage transcript and appearance of a newly abundant and several minor <it>msp2 </it>transcripts with high passage. BLASTN search of the <it>A. phagocytophilum </it>HZ strain genome revealed ≥ 52 <it>msp2 </it>paralogs.</p> <p>Conclusions</p> <p>Msp2 expression and <it>msp2 </it>transcription modulate even without immune selective pressures. However, the limited diversity of <it>msp2 </it>transcripts in the absence of immune pressure suggests selection for Msp2 by specific functions beyond that of immune evasion, in spite of a large genomic reservoir for Msp2 diversity.</p>
url http://www.biomedcentral.com/1471-2180/4/1
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