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Comparative genomics of Leishmania (Mundinia)

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Comparative genomics of Leishmania (Mundinia). / Butenko, A.; Kostygov, A.Y.; Sádlová, J. et al.
In: BMC Genomics, Vol. 20, No. 1, 726, 11.10.2019.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Butenko, A, Kostygov, AY, Sádlová, J, Kleschenko, Y, Bečvář, T, Podešvová, L, Macedo, DH, Žihala, D, Lukeš, J, Bates, PA, Volf, P, Opperdoes, FR & Yurchenko, V 2019, 'Comparative genomics of Leishmania (Mundinia)', BMC Genomics, vol. 20, no. 1, 726. https://doi.org/10.1186/s12864-019-6126-y

APA

Butenko, A., Kostygov, A. Y., Sádlová, J., Kleschenko, Y., Bečvář, T., Podešvová, L., Macedo, D. H., Žihala, D., Lukeš, J., Bates, P. A., Volf, P., Opperdoes, F. R., & Yurchenko, V. (2019). Comparative genomics of Leishmania (Mundinia). BMC Genomics, 20(1), Article 726. https://doi.org/10.1186/s12864-019-6126-y

Vancouver

Butenko A, Kostygov AY, Sádlová J, Kleschenko Y, Bečvář T, Podešvová L et al. Comparative genomics of Leishmania (Mundinia). BMC Genomics. 2019 Oct 11;20(1):726. doi: 10.1186/s12864-019-6126-y

Author

Butenko, A. ; Kostygov, A.Y. ; Sádlová, J. et al. / Comparative genomics of Leishmania (Mundinia). In: BMC Genomics. 2019 ; Vol. 20, No. 1.

Bibtex

@article{270487b45e9d422bb2d18dea38449ca9,
title = "Comparative genomics of Leishmania (Mundinia)",
abstract = "BackgroundTrypanosomatids of the genus Leishmania are parasites of mammals or reptiles transmitted by bloodsucking dipterans. Many species of these flagellates cause important human diseases with clinical symptoms ranging from skin sores to life-threatening damage of visceral organs. The genus Leishmania contains four subgenera: Leishmania, Sauroleishmania, Viannia, and Mundinia. The last subgenus has been established recently and remains understudied, although Mundinia contains human-infecting species. In addition, it is interesting from the evolutionary viewpoint, representing the earliest branch within the genus and possibly with a different type of vector. Here we analyzed the genomes of L. (M.) martiniquensis, L. (M.) enriettii and L. (M.) macropodum to better understand the biology and evolution of these parasites.ResultsAll three genomes analyzed were approximately of the same size (~ 30 Mb) and similar to that of L. (Sauroleishmania) tarentolae, but smaller than those of the members of subgenera Leishmania and Viannia, or the genus Endotrypanum (~ 32 Mb). This difference was explained by domination of gene losses over gains and contractions over expansions at the Mundinia node, although only a few of these genes could be identified. The analysis predicts significant changes in the Mundinia cell surface architecture, with the most important ones relating to losses of LPG-modifying side chain galactosyltransferases and arabinosyltransferases, as well as β-amastins. Among other important changes were gene family contractions for the oxygen-sensing adenylate cyclases and FYVE zinc finger-containing proteins.ConclusionsWe suggest that adaptation of Mundinia to different vectors and hosts has led to alternative host-parasite relationships and, thereby, made some proteins redundant. Thus, the evolution of genomes in the genus Leishmania and, in particular, in the subgenus Mundinia was mainly shaped by host (or vector) switches.",
keywords = "Whole genome sequencing, Leishmania (Mundinia) enriettii, L. (M.) macropodum, L. (M.) martiniquensis",
author = "A. Butenko and A.Y. Kostygov and J. S{\'a}dlov{\'a} and Y. Kleschenko and T. Be{\v c}v{\'a}{\v r} and L. Pode{\v s}vov{\'a} and D.H. Macedo and D. {\v Z}ihala and J. Luke{\v s} and P.A. Bates and P. Volf and F.R. Opperdoes and V. Yurchenko",
year = "2019",
month = oct,
day = "11",
doi = "10.1186/s12864-019-6126-y",
language = "English",
volume = "20",
journal = "BMC Genomics",
issn = "1471-2164",
publisher = "BioMed Central",
number = "1",

}

RIS

TY - JOUR

T1 - Comparative genomics of Leishmania (Mundinia)

AU - Butenko, A.

AU - Kostygov, A.Y.

AU - Sádlová, J.

AU - Kleschenko, Y.

AU - Bečvář, T.

AU - Podešvová, L.

AU - Macedo, D.H.

AU - Žihala, D.

AU - Lukeš, J.

AU - Bates, P.A.

AU - Volf, P.

AU - Opperdoes, F.R.

AU - Yurchenko, V.

PY - 2019/10/11

Y1 - 2019/10/11

N2 - BackgroundTrypanosomatids of the genus Leishmania are parasites of mammals or reptiles transmitted by bloodsucking dipterans. Many species of these flagellates cause important human diseases with clinical symptoms ranging from skin sores to life-threatening damage of visceral organs. The genus Leishmania contains four subgenera: Leishmania, Sauroleishmania, Viannia, and Mundinia. The last subgenus has been established recently and remains understudied, although Mundinia contains human-infecting species. In addition, it is interesting from the evolutionary viewpoint, representing the earliest branch within the genus and possibly with a different type of vector. Here we analyzed the genomes of L. (M.) martiniquensis, L. (M.) enriettii and L. (M.) macropodum to better understand the biology and evolution of these parasites.ResultsAll three genomes analyzed were approximately of the same size (~ 30 Mb) and similar to that of L. (Sauroleishmania) tarentolae, but smaller than those of the members of subgenera Leishmania and Viannia, or the genus Endotrypanum (~ 32 Mb). This difference was explained by domination of gene losses over gains and contractions over expansions at the Mundinia node, although only a few of these genes could be identified. The analysis predicts significant changes in the Mundinia cell surface architecture, with the most important ones relating to losses of LPG-modifying side chain galactosyltransferases and arabinosyltransferases, as well as β-amastins. Among other important changes were gene family contractions for the oxygen-sensing adenylate cyclases and FYVE zinc finger-containing proteins.ConclusionsWe suggest that adaptation of Mundinia to different vectors and hosts has led to alternative host-parasite relationships and, thereby, made some proteins redundant. Thus, the evolution of genomes in the genus Leishmania and, in particular, in the subgenus Mundinia was mainly shaped by host (or vector) switches.

AB - BackgroundTrypanosomatids of the genus Leishmania are parasites of mammals or reptiles transmitted by bloodsucking dipterans. Many species of these flagellates cause important human diseases with clinical symptoms ranging from skin sores to life-threatening damage of visceral organs. The genus Leishmania contains four subgenera: Leishmania, Sauroleishmania, Viannia, and Mundinia. The last subgenus has been established recently and remains understudied, although Mundinia contains human-infecting species. In addition, it is interesting from the evolutionary viewpoint, representing the earliest branch within the genus and possibly with a different type of vector. Here we analyzed the genomes of L. (M.) martiniquensis, L. (M.) enriettii and L. (M.) macropodum to better understand the biology and evolution of these parasites.ResultsAll three genomes analyzed were approximately of the same size (~ 30 Mb) and similar to that of L. (Sauroleishmania) tarentolae, but smaller than those of the members of subgenera Leishmania and Viannia, or the genus Endotrypanum (~ 32 Mb). This difference was explained by domination of gene losses over gains and contractions over expansions at the Mundinia node, although only a few of these genes could be identified. The analysis predicts significant changes in the Mundinia cell surface architecture, with the most important ones relating to losses of LPG-modifying side chain galactosyltransferases and arabinosyltransferases, as well as β-amastins. Among other important changes were gene family contractions for the oxygen-sensing adenylate cyclases and FYVE zinc finger-containing proteins.ConclusionsWe suggest that adaptation of Mundinia to different vectors and hosts has led to alternative host-parasite relationships and, thereby, made some proteins redundant. Thus, the evolution of genomes in the genus Leishmania and, in particular, in the subgenus Mundinia was mainly shaped by host (or vector) switches.

KW - Whole genome sequencing

KW - Leishmania (Mundinia) enriettii

KW - L. (M.) macropodum

KW - L. (M.) martiniquensis

U2 - 10.1186/s12864-019-6126-y

DO - 10.1186/s12864-019-6126-y

M3 - Journal article

VL - 20

JO - BMC Genomics

JF - BMC Genomics

SN - 1471-2164

IS - 1

M1 - 726

ER -