Strongyloides papillosus - PMC

Joel L. N. Barratt, Meredith Lane, Emir Talundzic, Travis Richins, Gemma Robertson, Fabio Formenti, Bobbi Pritt, Guilherme Verocai, Joelma Nascimento de Souza, Neci Mato Soares, Rebecca Traub, Dora Buonfrate, Richard S. Bradbury

PLoS Negl Trop Dis. 2019 Sep; 13(9): e0007609. Published online 2019 Sep 16. doi: 10.1371/journal.pntd.0007609

Correction in:: PLoS Negl Trop Dis. 2021 Jun; 15(6): e0009538.

PMCID:: PMC6762204

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Strongyloides RNA-seq Browser: a web-based software platform for on-demand bioinformatics analyses of Strongyloides species

Astra S Bryant, Stephanie F DeMarco, Elissa A Hallem

G3 (Bethesda) 2021 May; 11(5): jkab104. Published online 2021 Apr 6. doi: 10.1093/g3journal/jkab104

PMCID:: PMC8104939

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Using newly optimized genetic tools to probe Strongyloides sensory behaviors

Patricia Mendez, Breanna Walsh, Elissa A. Hallem

Mol Biochem Parasitol. 2022 Jul; 250: 111491. doi: 10.1016/j.molbiopara.2022.111491

PMCID:: PMC9339661

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The Impact of Acids Approved for Use in Foods on the Vitality of Haemonchus Contortus and Strongyloides Papillosus (Nematoda) Larvae

O. O. Boyko, V. V. Brygadyrenko

Helminthologia. 2019 Sep; 56(3): 202–210. Published online 2019 Sep 1. doi: 10.2478/helm-2019-0017

PMCID:: PMC6799582

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Strongyloides: omics to worm-free populations

Dora Buonfrate, Vicky L. Hunt, Peter Odermatt, Adrian Streit

Philos Trans R Soc Lond B Biol Sci. January 15, 2024; 379(1894): 20220448. Published online November 27, 2023. doi: 10.1098/rstb.2022.0448

PMCID:: PMC10676809

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Syntenic relationship of chromosomes in Strongyloides species and Rhabditophanes diutinus based on the chromosome-level genome assemblies

Asuka Kounosu, Simo Sun, Yasunobu Maeda, Mehmet Dayi, Akemi Yoshida, Haruhiko Maruyama, Vicky Hunt, Asako Sugimoto, Taisei Kikuchi

Philos Trans R Soc Lond B Biol Sci. January 15, 2024; 379(1894): 20220446. Published online November 27, 2023. doi: 10.1098/rstb.2022.0446

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Identification of miRNAs of Strongyloides stercoralis L1 and iL3 larvae isolated from human stool

Elena Pomari, Giovanni Malerba, Laura Veschetti, Alessandra Franceschi, Lucas Moron Dalla Tor, Michela Deiana, Monica Degani, Manuela Mistretta, Cristina Patuzzo, Andrea Ragusa, Antonio Mori, Zeno Bisoffi, Dora Buonfrate

Sci Rep. 2022; 12: 9957. Published online 2022 Jun 15. doi: 10.1038/s41598-022-14185-y

PMCID:: PMC9200769

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Karyotype and reproduction mode of the rodent parasite Strongyloides venezuelensis

AKINA HINO, TERUHISA TANAKA, MAHO TAKAISHI, YUMIKO FUJII, JUAN E. PALOMARES-RIUS, KOICHI HASEGAWA, HARUHIKO MARUYAMA, TAISEI KIKUCHI

Parasitology. 2014 Nov; 141(13): 1736–1745. Published online 2014 Aug 4. doi: 10.1017/S0031182014001036

PMCID:: PMC4183129

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The Genomic Basis of Parasitism in the Strongyloides Clade of Nematodes

Vicky L. Hunt, Isheng J. Tsai, Avril Coghlan, Adam J. Reid, Nancy Holroyd, Bernardo J. Foth, Alan Tracey, James A. Cotton, Eleanor J. Stanley, Helen Beasley, Hayley M. Bennett, Karen Brooks, Bhavana Harsha, Rei Kajitani, Arpita Kulkarni, Dorothee Harbecke, Eiji Nagayasu, Sarah Nichol, Yoshitoshi Ogura, Michael A. Quail, Nadine Randle, Dong Xia, Norbert W. Brattig, Hanns Soblik, Diogo M. Ribeiro, Alejandro Sanchez-Flores, Tetsuya Hayashi, Takehiko Itoh, Dee R. Denver, Warwick Grant, Jonathan D. Stoltzfus, James B. Lok, Haruhiko Murayama, Jonathan Wastling, Adrian Streit, Taisei Kikuchi, Mark Viney, Matthew Berriman

Nat Genet. Author manuscript; available in PMC 2016 Aug 10.

Published in final edited form as: Nat Genet. 2016 Mar; 48(3): 299–307. Published online 2016 Feb 1. doi: 10.1038/ng.3495

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Efficiency of the Bioverm^® (Duddingtonia flagrans) fungal formulation to control in vivo and in vitro of Haemonchus contortus and Strongyloides papillosus in sheep

Fábio Ribeiro Braga, Carolina Magri Ferraz, Edir Nepomuceno da Silva, Jackson Victor de Araújo

3 Biotech. 2020 Feb; 10(2): 62. Published online 2020 Jan 23. doi: 10.1007/s13205-019-2042-8

PMCID:: PMC6977787

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Molecular detection of Strongyloides sp. in Australian Thoroughbred foals

Ghazanfar Abbas, Abdul Ghafar, Anson V. Koehler, Jenni Bauquier, Edwina J. A. Wilkes, Caroline Jacobson, Anne Beasley, John Hurley, Lucy Cudmore, Peter Carrigan, Brett Tennent-Brown, Charles El-Hage, Martin K. Nielsen, Charles G. Gauci, Kristopher J. Hughes, Ian Beveridge, Abdul Jabbar

Parasit Vectors. 2021; 14: 444. Published online 2021 Sep 3. doi: 10.1186/s13071-021-04966-1

PMCID:: PMC8414860

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Germline organization in Strongyloides nematodes reveals alternative differentiation and regulation mechanisms

Arpita Kulkarni, James W. Lightfoot, Adrian Streit

Chromosoma. 2016; 125(4): 725–745. Published online 2015 Dec 12. doi: 10.1007/s00412-015-0562-5

PMCID:: PMC5023735

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Strongyloides questions—a research agenda for the future

Reem Al-Jawabreh, Roy Anderson, Louise E. Atkinson, Jack Bickford-Smith, Richard S. Bradbury, Minka Breloer, Astra S. Bryant, Dora Buonfrate, Luke C. Cadd, Bethany Crooks, Michela Deiana, Warwick Grant, Elissa Hallem, Shannon M. Hedtke, Vicky Hunt, Virak Khieu, Taisei Kikuchi, Asuka Kounosu, Dominika Lastik, Lisette van Lieshout, Yuchen Liu, Henry J. McSorley, Paul McVeigh, Angela Mousley, Ben Murcott, William David Nevin, Eva Nosková, Elena Pomari, Kieran Reynolds, Kirstin Ross, Adrian Streit, Mona Suleiman, Natalia Tiberti, Mark Viney

Philos Trans R Soc Lond B Biol Sci. January 15, 2024; 379(1894): 20230004. Published online November 27, 2023. doi: 10.1098/rstb.2023.0004

PMCID:: PMC10676812

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Gene Silencing and Sex Determination by Programmed DNA Elimination in Parasitic Nematodes

Adrian Streit, Jianbin Wang, Yuanyuan Kang, Richard E. Davis

Curr Opin Microbiol. Author manuscript; available in PMC 2017 Aug 1.

Published in final edited form as: Curr Opin Microbiol. 2016 Aug; 32: 120–127. Published online 2016 Jun 14. doi: 10.1016/j.mib.2016.05.012

PMCID:: PMC4983467

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A Conserved Endocrine Mechanism Controls the Formation of Dauer and Infective Larvae in Nematodes

Akira Ogawa, Adrian Streit, Adam Antebi, Ralf J. Sommer

Curr Biol. Author manuscript; available in PMC 2010 Jan 13.

Published in final edited form as: Curr Biol. 2009 Jan 13; 19(1): 67–71. Published online 2008 Dec 24. doi: 10.1016/j.cub.2008.11.063

PMCID:: PMC2712670

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Figure-3

Strongyloides papillosus egg with larva inside (×400).

Prevalence of Cryptosporidia, Eimeria, Giardia, and Strongyloides in pre-weaned calves on smallholder dairy farms in Mukurwe-ini district, Kenya

Vet World. 2015 Sep;8(9):1118-1125.
F ig . 1.—

The life cycle of S. papillosus. (A) The life cycle of S. papillosus consists of free-living and parasitic stages. Parasitic worms are female only. Within the host, parasitic females reproduce clonally. Their female offspring can either develop directly into infective larvae (iL3) or develop into facultative free-living females that reproduce sexually with males (indirect cycle). Their progeny develops into iL3. Stages for which transcriptomes were sequenced are labeled with #. (B) The schematic tree shows the phylogenetic relationships between different Strongyloides species (). The species that are subject of this study are highlighted by a box.

Duplications and Positive Selection Drive the Evolution of Parasitism-Associated Gene Families in the Nematode Strongyloides papillosus

Genome Biol Evol. 2017 Mar;9(3):790-801.
Fig 1daf-12 homologs in four species of Strongyloides.

A) Schematic representation of the DAF-12 proteins. Amino acid identities with C. elegans are given for the DNA binding domain (DBD) and for the ligand binding domain (LBD). The species prefixes are Sra S. ratti, Spa S. papillosus, Sst S. stercoralis and Sve S. venezuelensis. B) Gene models of the daf-12 homologs in Strongyloides. spp. Notice that, daf-12 within S. ratti, S. stercoralis and S. venezuelensis all have a large intron between their first and second exons unlike S. papillosus which lacks this feature. However the size of the S. papillosus protein (719 amino acids) is still similar to that of S. ratti (749 amino acids). The labels are the gene identifiers according to WormBase ParaSite (https://parasite.wormbase.org/index.html) containing the species codes SRAE S. ratti, SPAL S. papillosus, SSTP S. stercoralis and SVE S. venezuelensis. Scale bar = 100bp.

RNAi-mediated knockdown of daf-12 in the model parasitic nematode Strongyloides ratti

PLoS Pathog. 2019 Mar;15(3):e1007705.
Fig. 5

a Stereomicroscopic observation set up. It is important that the illumination is from underneath. b Free-living adults of S. stercoralis under the stereo dissecting microscopy at low magnification. c Morphology of free-living adults and iL3 of Strongyloides (shown are differential interference contrast (DIC) images of S. papillosus)

From the feces to the genome: a guideline for the isolation and preservation of Strongyloides stercoralis in the field for genetic and genomic analysis of individual worms

Parasit Vectors. 2019;12:496.