Analysis of pir gene expression across the Plasmodium life cycle
Abstract Background Plasmodium interspersed repeat (pir) is the largest multigene family in the genomes of most Plasmodium species. A variety of functions for the PIR proteins which they encode have been proposed, including antigenic variation, immune evasion, sequestration and rosetting. However, d...
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oai:doaj.org-article:9efaea334f8249f48589d96afa34ed432021-11-28T12:30:48ZAnalysis of pir gene expression across the Plasmodium life cycle10.1186/s12936-021-03979-61475-2875https://doaj.org/article/9efaea334f8249f48589d96afa34ed432021-11-01T00:00:00Zhttps://doi.org/10.1186/s12936-021-03979-6https://doaj.org/toc/1475-2875Abstract Background Plasmodium interspersed repeat (pir) is the largest multigene family in the genomes of most Plasmodium species. A variety of functions for the PIR proteins which they encode have been proposed, including antigenic variation, immune evasion, sequestration and rosetting. However, direct evidence for these is lacking. The repetitive nature of the family has made it difficult to determine function experimentally. However, there has been some success in using gene expression studies to suggest roles for some members in virulence and chronic infection. Methods Here pir gene expression was examined across the life cycle of Plasmodium berghei using publicly available RNAseq data-sets, and at high resolution in the intraerythrocytic development cycle using new data from Plasmodium chabaudi. Results Expression of pir genes is greatest in stages of the parasite which invade and reside in red blood cells. The marked exception is that liver merozoites and male gametocytes produce a very large number of pir gene transcripts, notably compared to female gametocytes, which produce relatively few. Within the asexual blood stages different subfamilies peak at different times, suggesting further functional distinctions. Representing a subfamily of its own, the highly conserved ancestral pir gene warrants further investigation due to its potential tractability for functional investigation. It is highly transcribed in multiple life cycle stages and across most studied Plasmodium species and thus is likely to play an important role in parasite biology. Conclusions The identification of distinct expression patterns for different pir genes and subfamilies is likely to provide a basis for the design of future experiments to uncover their function.Timothy S. LittleDeirdre A. CunninghamAudrey VandommeCarlos Talavera LopezSarah AmisChristopher AlderJohn W. G. AddySarah McLaughlinCaroline HoskingGeorge ChristophidesAdam J. ReidJean LanghorneBMCarticleArctic medicine. Tropical medicineRC955-962Infectious and parasitic diseasesRC109-216ENMalaria Journal, Vol 20, Iss 1, Pp 1-14 (2021) |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 Timothy S. Little Deirdre A. Cunningham Audrey Vandomme Carlos Talavera Lopez Sarah Amis Christopher Alder John W. G. Addy Sarah McLaughlin Caroline Hosking George Christophides Adam J. Reid Jean Langhorne Analysis of pir gene expression across the Plasmodium life cycle |
description |
Abstract Background Plasmodium interspersed repeat (pir) is the largest multigene family in the genomes of most Plasmodium species. A variety of functions for the PIR proteins which they encode have been proposed, including antigenic variation, immune evasion, sequestration and rosetting. However, direct evidence for these is lacking. The repetitive nature of the family has made it difficult to determine function experimentally. However, there has been some success in using gene expression studies to suggest roles for some members in virulence and chronic infection. Methods Here pir gene expression was examined across the life cycle of Plasmodium berghei using publicly available RNAseq data-sets, and at high resolution in the intraerythrocytic development cycle using new data from Plasmodium chabaudi. Results Expression of pir genes is greatest in stages of the parasite which invade and reside in red blood cells. The marked exception is that liver merozoites and male gametocytes produce a very large number of pir gene transcripts, notably compared to female gametocytes, which produce relatively few. Within the asexual blood stages different subfamilies peak at different times, suggesting further functional distinctions. Representing a subfamily of its own, the highly conserved ancestral pir gene warrants further investigation due to its potential tractability for functional investigation. It is highly transcribed in multiple life cycle stages and across most studied Plasmodium species and thus is likely to play an important role in parasite biology. Conclusions The identification of distinct expression patterns for different pir genes and subfamilies is likely to provide a basis for the design of future experiments to uncover their function. |
format |
article |
author |
Timothy S. Little Deirdre A. Cunningham Audrey Vandomme Carlos Talavera Lopez Sarah Amis Christopher Alder John W. G. Addy Sarah McLaughlin Caroline Hosking George Christophides Adam J. Reid Jean Langhorne |
author_facet |
Timothy S. Little Deirdre A. Cunningham Audrey Vandomme Carlos Talavera Lopez Sarah Amis Christopher Alder John W. G. Addy Sarah McLaughlin Caroline Hosking George Christophides Adam J. Reid Jean Langhorne |
author_sort |
Timothy S. Little |
title |
Analysis of pir gene expression across the Plasmodium life cycle |
title_short |
Analysis of pir gene expression across the Plasmodium life cycle |
title_full |
Analysis of pir gene expression across the Plasmodium life cycle |
title_fullStr |
Analysis of pir gene expression across the Plasmodium life cycle |
title_full_unstemmed |
Analysis of pir gene expression across the Plasmodium life cycle |
title_sort |
analysis of pir gene expression across the plasmodium life cycle |
publisher |
BMC |
publishDate |
2021 |
url |
https://doaj.org/article/9efaea334f8249f48589d96afa34ed43 |
work_keys_str_mv |
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