Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains
Background: Xanthomonas citri, a causal agent of citrus canker, has been a well-studied model system due to recent availability of whole genome sequences of multiple strains from different geographical regions. Major limitations in our understanding of the evolution of pathogenicity factors in X. citri strains sequenced by short-read sequencing methods have been tracking plasmid reshuffling among strains due to inability to accurately assign reads to plasmids, and analyzing repeat regions among strains. X. citri harbors major pathogenicity determinants, including variable DNA-binding repeat region containing Transcription Activator-like Effectors (TALEs) on plasmids. The long-read sequencing method, PacBio, has allowed the ability to obtain complete and accurate sequences of TALEs in xanthomonads. We recently sequenced Xanthomonas citri str. Xc-03-1638-1-1, a copper tolerant A group strain isolated from grapefruit in 2003 from Argentina using PacBio RS II chemistry. We analyzed plasmid profiles, copy number and location of TALEs in complete genome sequences of X. citri strains. Results: We utilized the power of long reads obtained by PacBio sequencing to enable assembly of a complete genome sequence of strain Xc-03-1638-1-1, including sequences of two plasmids, 249 kb (plasmid harboring copper resistance genes) and 99 kb (pathogenicity plasmid containing TALEs). The pathogenicity plasmid in this strain is a hybrid plasmid containing four TALEs. Due to the intriguing nature of this pathogenicity plasmid with Tn3-like transposon association, repetitive elements and multiple putative sites for origins of replication, we might expect alternative structures of this plasmid in nature, illustrating the strong adaptive potential of X. citri strains. Analysis of the pathogenicity plasmid among completely sequenced X. citri strains, coupled with Southern hybridization of the pathogenicity plasmids, revealed clues to rearrangements of plasmids and resulting reshuffling of TALEs among strains. Conclusions: We demonstrate in this study the importance of long-read sequencing for obtaining intact sequences of TALEs and plasmids, as well as for identifying rearrangement events including plasmid reshuffling. Rearrangement events, such as the hybrid plasmid in this case, could be a frequent phenomenon in the evolution of X. citri strains, although so far it is undetected due to the inability to obtain complete plasmid sequences with short-read sequencing methods.
Main Authors: | , , , , , , , , , , |
---|---|
Format: | info:ar-repo/semantics/artículo biblioteca |
Language: | eng |
Published: |
BioMed Central
2018
|
Subjects: | Xanthomonas Campestris Citri, Cobre, Patogenicidad, Plasmidios, Copper, Pathogenicity, Plasmids, Citrus Canker, pthA, PacBio, Generation Sequencing NGS, Cancrosis de los Citrus, |
Online Access: | http://hdl.handle.net/20.500.12123/3537 https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-017-4408-9 https://doi.org/10.1186/s12864-017-4408-9 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
oai:localhost:20.500.12123-3537 |
---|---|
record_format |
koha |
institution |
INTA AR |
collection |
DSpace |
country |
Argentina |
countrycode |
AR |
component |
Bibliográfico |
access |
En linea |
databasecode |
dig-inta-ar |
tag |
biblioteca |
region |
America del Sur |
libraryname |
Biblioteca Central del INTA Argentina |
language |
eng |
topic |
Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus |
spellingShingle |
Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus Gochez, Alberto Martin Huguet-Tapia, Jose Carlos Minsavage, Gerald V. Shantharaj, Deepak Jalan, Neha Strauß, Annett Lahaye, Thomas Wang, Nian Canteros, Blanca Isabel Jones, Jeffrey B. Potnis, Neha Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
description |
Background:
Xanthomonas citri, a causal agent of citrus canker, has been a well-studied model system due to recent availability of whole genome sequences of multiple strains from different geographical regions. Major limitations in our understanding of the evolution of pathogenicity factors in X. citri strains sequenced by short-read sequencing methods have been tracking plasmid reshuffling among strains due to inability to accurately assign reads to plasmids, and analyzing repeat regions among strains. X. citri harbors major pathogenicity determinants, including variable DNA-binding repeat region containing Transcription Activator-like Effectors (TALEs) on plasmids. The long-read sequencing method, PacBio, has allowed the ability to obtain complete and accurate sequences of TALEs in xanthomonads. We recently sequenced Xanthomonas citri str. Xc-03-1638-1-1, a copper tolerant A group strain isolated from grapefruit in 2003 from Argentina using PacBio RS II chemistry. We analyzed plasmid profiles, copy number and location of TALEs in complete genome sequences of X. citri strains.
Results:
We utilized the power of long reads obtained by PacBio sequencing to enable assembly of a complete genome sequence of strain Xc-03-1638-1-1, including sequences of two plasmids, 249 kb (plasmid harboring copper resistance genes) and 99 kb (pathogenicity plasmid containing TALEs). The pathogenicity plasmid in this strain is a hybrid plasmid containing four TALEs. Due to the intriguing nature of this pathogenicity plasmid with Tn3-like transposon association, repetitive elements and multiple putative sites for origins of replication, we might expect alternative structures of this plasmid in nature, illustrating the strong adaptive potential of X. citri strains. Analysis of the pathogenicity plasmid among completely sequenced X. citri strains, coupled with Southern hybridization of the pathogenicity plasmids, revealed clues to rearrangements of plasmids and resulting reshuffling of TALEs among strains.
Conclusions:
We demonstrate in this study the importance of long-read sequencing for obtaining intact sequences of TALEs and plasmids, as well as for identifying rearrangement events including plasmid reshuffling. Rearrangement events, such as the hybrid plasmid in this case, could be a frequent phenomenon in the evolution of X. citri strains, although so far it is undetected due to the inability to obtain complete plasmid sequences with short-read sequencing methods. |
format |
info:ar-repo/semantics/artículo |
topic_facet |
Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus |
author |
Gochez, Alberto Martin Huguet-Tapia, Jose Carlos Minsavage, Gerald V. Shantharaj, Deepak Jalan, Neha Strauß, Annett Lahaye, Thomas Wang, Nian Canteros, Blanca Isabel Jones, Jeffrey B. Potnis, Neha |
author_facet |
Gochez, Alberto Martin Huguet-Tapia, Jose Carlos Minsavage, Gerald V. Shantharaj, Deepak Jalan, Neha Strauß, Annett Lahaye, Thomas Wang, Nian Canteros, Blanca Isabel Jones, Jeffrey B. Potnis, Neha |
author_sort |
Gochez, Alberto Martin |
title |
Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
title_short |
Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
title_full |
Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
title_fullStr |
Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
title_full_unstemmed |
Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains |
title_sort |
pacbio sequencing of copper-tolerant xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among x. citri strains |
publisher |
BioMed Central |
publishDate |
2018 |
url |
http://hdl.handle.net/20.500.12123/3537 https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-017-4408-9 https://doi.org/10.1186/s12864-017-4408-9 |
work_keys_str_mv |
AT gochezalbertomartin pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT huguettapiajosecarlos pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT minsavagegeraldv pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT shantharajdeepak pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT jalanneha pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT straußannett pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT lahayethomas pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT wangnian pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT canterosblancaisabel pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT jonesjeffreyb pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains AT potnisneha pacbiosequencingofcoppertolerantxanthomonascitrirevealspresenceofachimericplasmidstructureandprovidesinsightsintoreassortmentandshufflingoftranscriptionactivatorlikeeffectorsamongxcitristrains |
_version_ |
1756007268861607936 |
spelling |
oai:localhost:20.500.12123-35372018-10-02T14:41:41Z Pacbio sequencing of copper-tolerant Xanthomonas citri reveals presence of a chimeric plasmid structure and provides insights into reassortment and shuffling of transcription activator-like effectors among X. citri strains Gochez, Alberto Martin Huguet-Tapia, Jose Carlos Minsavage, Gerald V. Shantharaj, Deepak Jalan, Neha Strauß, Annett Lahaye, Thomas Wang, Nian Canteros, Blanca Isabel Jones, Jeffrey B. Potnis, Neha Xanthomonas Campestris Citri Cobre Patogenicidad Plasmidios Copper Pathogenicity Plasmids Citrus Canker pthA PacBio Generation Sequencing NGS Cancrosis de los Citrus Background: Xanthomonas citri, a causal agent of citrus canker, has been a well-studied model system due to recent availability of whole genome sequences of multiple strains from different geographical regions. Major limitations in our understanding of the evolution of pathogenicity factors in X. citri strains sequenced by short-read sequencing methods have been tracking plasmid reshuffling among strains due to inability to accurately assign reads to plasmids, and analyzing repeat regions among strains. X. citri harbors major pathogenicity determinants, including variable DNA-binding repeat region containing Transcription Activator-like Effectors (TALEs) on plasmids. The long-read sequencing method, PacBio, has allowed the ability to obtain complete and accurate sequences of TALEs in xanthomonads. We recently sequenced Xanthomonas citri str. Xc-03-1638-1-1, a copper tolerant A group strain isolated from grapefruit in 2003 from Argentina using PacBio RS II chemistry. We analyzed plasmid profiles, copy number and location of TALEs in complete genome sequences of X. citri strains. Results: We utilized the power of long reads obtained by PacBio sequencing to enable assembly of a complete genome sequence of strain Xc-03-1638-1-1, including sequences of two plasmids, 249 kb (plasmid harboring copper resistance genes) and 99 kb (pathogenicity plasmid containing TALEs). The pathogenicity plasmid in this strain is a hybrid plasmid containing four TALEs. Due to the intriguing nature of this pathogenicity plasmid with Tn3-like transposon association, repetitive elements and multiple putative sites for origins of replication, we might expect alternative structures of this plasmid in nature, illustrating the strong adaptive potential of X. citri strains. Analysis of the pathogenicity plasmid among completely sequenced X. citri strains, coupled with Southern hybridization of the pathogenicity plasmids, revealed clues to rearrangements of plasmids and resulting reshuffling of TALEs among strains. Conclusions: We demonstrate in this study the importance of long-read sequencing for obtaining intact sequences of TALEs and plasmids, as well as for identifying rearrangement events including plasmid reshuffling. Rearrangement events, such as the hybrid plasmid in this case, could be a frequent phenomenon in the evolution of X. citri strains, although so far it is undetected due to the inability to obtain complete plasmid sequences with short-read sequencing methods. EEA Bella Vista Fil: Gochez, Alberto Martin. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Bella Vista; Argentina Fil: Huguet-Tapia, Jose Carlos. University of Florida. Department of Plant Pathology; Estados Unidos Fil: Minsavage, Gerald V. University of Florida. Department of Plant Pathology; Estados Unidos Fil: Shantharaj, Deepak. University of Florida. Department of Plant Pathology; Estados Unidos Fil: Jalan, Neha. University of Florida. Department of Microbiology and Cell Science. Citrus Research and Education Center; Estados Unidos Fil: Strauß, Annett. University of Tübingen; Alemania Fil: Lahaye, Thomas. University of Tübingen; Alemania Fil: Wang, Nian. University of Florida. Department of Microbiology and Cell Science. Citrus Research and Education Center; Estados Unidos Fil: Canteros, Blanca Isabel. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Bella Vista; Argentina Fil: Jones, Jeffrey B. University of Florida. Department of Plant Pathology; Estados Unidos Fil: Potnis, Neha. Auburn University. Department of Entomology and Plant Pathology; Estados Unidos 2018-10-02T14:35:32Z 2018-10-02T14:35:32Z 2018 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://hdl.handle.net/20.500.12123/3537 https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-017-4408-9 1471-2164 https://doi.org/10.1186/s12864-017-4408-9 eng info:eu-repo/semantics/openAccess application/pdf BioMed Central BMC Genomics 19:16. (2018) |