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Nycteria Parasites of Afrotropical Insectivorous Bats Q ⇑ Juliane Schaer A,B, , Deeann M
International Journal for Parasitology xxx (2015) xxx–xxx Contents lists available at ScienceDirect International Journal for Parasitology journal homepage: www.elsevier.com/locate/ijpara Nycteria parasites of Afrotropical insectivorous bats q ⇑ Juliane Schaer a,b, , DeeAnn M. Reeder c, Megan E. Vodzak c, Kevin J. Olival d, Natalie Weber e, Frieder Mayer b, Kai Matuschewski a,f, Susan L. Perkins g a Max Planck Institute for Infection Biology, Parasitology Unit, 10117 Berlin, Germany b Museum für Naturkunde – Leibniz Institute for Research on Evolution and Biodiversity, 10115 Berlin, Germany c Department of Biology, Bucknell University, Lewisburg, PA 17837, USA d EcoHealth Alliance, New York, NY 10001, USA e Institute of Experimental Ecology, University of Ulm, 89069 Ulm, Germany f Institute of Biology, Humboldt University, 10117 Berlin, Germany g Sackler Institute for Comparative Genomics, American Museum of Natural History, New York, NY 10024, USA article info abstract Article history: Parasitic protozoan parasites have evolved many co-evolutionary paths towards stable transmission to Received 12 October 2014 their host population. Plasmodium spp., the causative agents of malaria, and related haemosporidian Received in revised form 13 January 2015 parasites are dipteran-borne eukaryotic pathogens that actively invade and use vertebrate erythrocytes Accepted 17 January 2015 for gametogenesis and asexual development, often resulting in substantial morbidity and mortality of Available online xxxx the infected hosts. Here, we present results of a survey of insectivorous bats from tropical Africa, includ- ing new isolates of species of the haemosporidian genus Nycteria. A hallmark of these parasites is their Keywords: capacity to infect bat species of distinct families of the two evolutionary distant chiropteran suborders. -
Plasmodium Asexual Growth and Sexual Development in the Haematopoietic Niche of the Host
REVIEWS Plasmodium asexual growth and sexual development in the haematopoietic niche of the host Kannan Venugopal 1, Franziska Hentzschel1, Gediminas Valkiūnas2 and Matthias Marti 1* Abstract | Plasmodium spp. parasites are the causative agents of malaria in humans and animals, and they are exceptionally diverse in their morphology and life cycles. They grow and develop in a wide range of host environments, both within blood- feeding mosquitoes, their definitive hosts, and in vertebrates, which are intermediate hosts. This diversity is testament to their exceptional adaptability and poses a major challenge for developing effective strategies to reduce the disease burden and transmission. Following one asexual amplification cycle in the liver, parasites reach high burdens by rounds of asexual replication within red blood cells. A few of these blood- stage parasites make a developmental switch into the sexual stage (or gametocyte), which is essential for transmission. The bone marrow, in particular the haematopoietic niche (in rodents, also the spleen), is a major site of parasite growth and sexual development. This Review focuses on our current understanding of blood-stage parasite development and vascular and tissue sequestration, which is responsible for disease symptoms and complications, and when involving the bone marrow, provides a niche for asexual replication and gametocyte development. Understanding these processes provides an opportunity for novel therapies and interventions. Gametogenesis Malaria is one of the major life- threatening infectious Malaria parasites have a complex life cycle marked Maturation of male and female diseases in humans and is particularly prevalent in trop- by successive rounds of asexual replication across gametes. ical and subtropical low- income regions of the world. -
Highly Rearranged Mitochondrial Genome in Nycteria Parasites (Haemosporidia) from Bats
Highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats Gregory Karadjiana,1,2, Alexandre Hassaninb,1, Benjamin Saintpierrec, Guy-Crispin Gembu Tungalunad, Frederic Arieye, Francisco J. Ayalaf,3, Irene Landaua, and Linda Duvala,3 aUnité Molécules de Communication et Adaptation des Microorganismes (UMR 7245), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, CP52, 75005 Paris, France; bInstitut de Systématique, Evolution, Biodiversité (UMR 7205), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, Université Pierre et Marie Curie, CP51, 75005 Paris, France; cUnité de Génétique et Génomique des Insectes Vecteurs (CNRS URA3012), Département de Parasites et Insectes Vecteurs, Institut Pasteur, 75015 Paris, France; dFaculté des Sciences, Université de Kisangani, BP 2012 Kisangani, Democratic Republic of Congo; eLaboratoire de Biologie Cellulaire Comparative des Apicomplexes, Faculté de Médicine, Université Paris Descartes, Inserm U1016, CNRS UMR 8104, Cochin Institute, 75014 Paris, France; and fDepartment of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697 Contributed by Francisco J. Ayala, July 6, 2016 (sent for review March 18, 2016; reviewed by Sargis Aghayan and Georges Snounou) Haemosporidia parasites have mostly and abundantly been de- and this lack of knowledge limits the understanding of the scribed using mitochondrial genes, and in particular cytochrome evolutionary history of Haemosporidia, in particular their b (cytb). Failure to amplify the mitochondrial cytb gene of Nycteria basal diversification. parasites isolated from Nycteridae bats has been recently reported. Nycteria parasites have been primarily described, based on Bats are hosts to a diverse and profuse array of Haemosporidia traditional taxonomy, in African insectivorous bats of two fami- parasites that remain largely unstudied. -
A Highly Rearranged Mitochondrial Genome in Nycteria Parasites
A highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats Gregory Karadjian, Alexandre Hassanin, Benjamin Saintpierre, Guy-Crispin Gembu Tungaluna, Frederic Ariey, Francisco J. Ayala, Irene Landau, Linda Duval To cite this version: Gregory Karadjian, Alexandre Hassanin, Benjamin Saintpierre, Guy-Crispin Gembu Tungaluna, Fred- eric Ariey, et al.. A highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2016, 113 (35), pp.9834 - 9839. 10.1073/pnas.1610643113. hal-01395176 HAL Id: hal-01395176 https://hal.sorbonne-universite.fr/hal-01395176 Submitted on 10 Nov 2016 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - NonCommercial| 4.0 International License A highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats Gregory Karadjian a, b, 1, Alexandre Hassaninc, 1, Benjamin Saintpierred, Guy-Crispin Gembu -
Endoparasites
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications from the Harold W. Manter Laboratory of Parasitology Parasitology, Harold W. Manter Laboratory of 1979 Endoparasites John E. Ubelaker Southern Methodist University, [email protected] Robert D. Specian Louisiana State University Health Sciences Center - Shreveport, [email protected] Donald W. Duszynski University of New Mexico, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/parasitologyfacpubs Part of the Parasitology Commons Ubelaker, John E.; Specian, Robert D.; and Duszynski, Donald W., "Endoparasites" (1979). Faculty Publications from the Harold W. Manter Laboratory of Parasitology. 677. https://digitalcommons.unl.edu/parasitologyfacpubs/677 This Article is brought to you for free and open access by the Parasitology, Harold W. Manter Laboratory of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications from the Harold W. Manter Laboratory of Parasitology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Published in Biology of bats of the New World family Phyllostomatidae, Part III (Robert J. Baker, J. Knox Jones, Jr., and Dilford C. Carter eds.), Special Publications of the Museum, Texas Tech University, 16:1-441, January 12, 1979. ENDOP ARASITES JOHN E. UBELAKER, ROBERT D. SPECIAN, AND DONALD W. DUSZYNSKI The leaf-nosed bats of the New World family Phyllostomatidae occur from the southwestern United States through tropical Central and South America. Mem bers of this family are also found throughout the Antilles. The ecological associa tions of the species in this family seem to be rather broad; species are found in humid tropical to semiarid and arid subtropical environments. -
AMNH-Scientific-Publications-2014
AMERICAN MUSEUM OF NATURAL HISTORY Fiscal Year 2014 Scientific Publications Division of Anthropology 2 Division of Invertebrate Zoology 11 Division of Paleontology 28 Division of Physical Sciences 39 Department of Earth and Planetary Sciences and Department of Astrophysics Division of Vertebrate Zoology Department of Herpetology 58 Department of Ichthyology 62 Department of Mammalogy 65 Department of Ornithology 78 Center for Biodiversity and Conservation 91 Sackler Institute for Comparative Genomics 99 DIVISION OF ANTHROPOLOGY Berwick, R.C., M.D. Hauser, and I. Tattersall. 2013. Neanderthal language? Just-so stories take center stage. Frontiers in Psychology 4, article 671. Blair, E.H., and Thomas, D.H. 2014. The Guale uprising of 1597: an archaeological perspective from Mission Santa Catalina de Guale (Georgia). In L.M. Panich and T.D. Schneider (editors), Indigenous Landscapes and Spanish Missions: New Perspectives from Archaeology and Ethnohistory: 25–40. Tucson: University of Arizona Press. Charpentier, V., A.J. de Voogt, R. Crassard, J.-F. Berger, F. Borgi, and A. Al- Ma’shani. 2014. Games on the seashore of Salalah: the discovery of mancala games in Dhofar, Sultanate of Oman. Arabian Archaeology and Epigraphy 25: 115– 120. Chowns, T.M., A.H. Ivester, R.L. Kath, B.K. Meyer, D.H. Thomas, and P.R. Hanson. 2014. A New Hypothesis for the Formation of the Georgia Sea Islands through the Breaching of the Silver Bluff Barrier and Dissection of the Ancestral Altamaha-Ogeechee Drainage. Abstract, 63rd Annual Meeting, Geological Society of America, Southeastern Section, April 10–11, 2014. 2 DeSalle, R., and I. Tattersall. 2014. Mr. Murray, you lose the bet. -
Highly Rearranged Mitochondrial Genome in Nycteria Parasites (Haemosporidia) from Bats
Highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats Gregory Karadjiana,1,2, Alexandre Hassaninb,1, Benjamin Saintpierrec, Guy-Crispin Gembu Tungalunad, Frederic Arieye, Francisco J. Ayalaf,3, Irene Landaua, and Linda Duvala,3 aUnité Molécules de Communication et Adaptation des Microorganismes (UMR 7245), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, CP52, 75005 Paris, France; bInstitut de Systématique, Evolution, Biodiversité (UMR 7205), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, Université Pierre et Marie Curie, CP51, 75005 Paris, France; cUnité de Génétique et Génomique des Insectes Vecteurs (CNRS URA3012), Département de Parasites et Insectes Vecteurs, Institut Pasteur, 75015 Paris, France; dFaculté des Sciences, Université de Kisangani, BP 2012 Kisangani, Democratic Republic of Congo; eLaboratoire de Biologie Cellulaire Comparative des Apicomplexes, Faculté de Médicine, Université Paris Descartes, Inserm U1016, CNRS UMR 8104, Cochin Institute, 75014 Paris, France; and fDepartment of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697 Contributed by Francisco J. Ayala, July 6, 2016 (sent for review March 18, 2016; reviewed by Sargis Aghayan and Georges Snounou) Haemosporidia parasites have mostly and abundantly been de- and this lack of knowledge limits the understanding of the scribed using mitochondrial genes, and in particular cytochrome evolutionary history of Haemosporidia, in particular their b (cytb). Failure to amplify the mitochondrial cytb gene of Nycteria basal diversification. parasites isolated from Nycteridae bats has been recently reported. Nycteria parasites have been primarily described, based on Bats are hosts to a diverse and profuse array of Haemosporidia traditional taxonomy, in African insectivorous bats of two fami- parasites that remain largely unstudied. -
Parasitaemia Data and Molecular Characterization of Haemoproteus Catharti from New World Vultures (Cathartidae) Reveals a Novel Clade of Haemosporida
Faculty Scholarship 2018 Parasitaemia data and molecular characterization of Haemoproteus catharti from New World vultures (Cathartidae) reveals a novel clade of Haemosporida Michael J. Yabsley Ralph E.T. Vanstreels Ellen S. Martinsen Alexandra G. Wickson Amanda E. Holland See next page for additional authors Follow this and additional works at: https://researchrepository.wvu.edu/faculty_publications Part of the Agriculture Commons, Biology Commons, Ecology and Evolutionary Biology Commons, Forest Sciences Commons, and the Marine Biology Commons Authors Michael J. Yabsley, Ralph E.T. Vanstreels, Ellen S. Martinsen, Alexandra G. Wickson, Amanda E. Holland, Sonia M. Hernandez, Alec T. Thompson, Susan L. Perkins, Christopher A. Lawrence Bryan, Christopher A. Cleveland, Emily Jolly, Justin D. Brown, Dave McRuer, Shannon Behmke, and James C. Beasley Yabsley et al. Malar J (2018) 17:12 https://doi.org/10.1186/s12936-017-2165-5 Malaria Journal RESEARCH Open Access Parasitaemia data and molecular characterization of Haemoproteus catharti from New World vultures (Cathartidae) reveals a novel clade of Haemosporida Michael J. Yabsley1,2* , Ralph E. T. Vanstreels3,4, Ellen S. Martinsen5,6, Alexandra G. Wickson1, Amanda E. Holland1,7, Sonia M. Hernandez1,2, Alec T. Thompson1, Susan L. Perkins8, Christopher J. West9, A. Lawrence Bryan7, Christopher A. Cleveland1,2, Emily Jolly1, Justin D. Brown10, Dave McRuer11, Shannon Behmke12 and James C. Beasley1,7 Abstract Background: New World vultures (Cathartiformes: Cathartidae) are obligate scavengers comprised of seven species in fve genera throughout the Americas. Of these, turkey vultures (Cathartes aura) and black vultures (Coragyps atratus) are the most widespread and, although ecologically similar, have evolved diferences in morphology, physiology, and behaviour. -
The Genome of Haemoproteus Tartakovskyi and Its Relationship To
GBE TheGenomeofHaemoproteus tartakovskyi and Its Relationship to Human Malaria Parasites Staffan Bensch1,*,Bjo¨ rn Canba¨ck1, Jeremy D. DeBarry2, Tomas Johansson1, Olof Hellgren1, Jessica C. Kissinger2,3, Vaidas Palinauskas4, Elin Videvall1, and Gediminas Valkiu¯ nas4 1Department of Biology, Lund University, Sweden 2The Center for Tropical and Emerging Global Diseases, Athens, Georgia, USA 3Department of Genetics and Institute of Bioinformatics, University of Georgia Downloaded from https://academic.oup.com/gbe/article/8/5/1361/2939581 by guest on 02 October 2021 4Nature Research Centre, Vilnius, Lithuania *Corresponding author: E-mail: [email protected]. Data deposition: Haemoproteus tartakovskyi: The Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under the accession LSRZ00000000. The version described in this paper is version LSRZ01000000. The genome assembly with predicted genes are available for download at http://mbio-serv2.mbioekol.lu.se/Malavi/Downloads. Plasmodium ashfordi: This project has been deposited at: the NCBI Sequence Read Archive under the accession number PRJNA311546. The assembled transcripts are available for download at http://mbio-serv2.mbioekol.lu.se/Malavi/Downloads. Accepted: April 4, 2016 Abstract The phylogenetic relationships among hemosporidian parasites, including the origin of Plasmodium falciparum,themostvirulent malaria parasite of humans, have been heavily debated for decades. Studies based on multiple-gene sequences have helped settle many of these controversial phylogenetic issues. However, denser taxon sampling and genome-wide analyses are needed to con- fidently resolve the evolutionay relationships among hemosporidian parasites. Genome sequences of several Plasmodium parasites are available but only for species infecting primates and rodents. To root the phylogenetic tree of Plasmodium, genomic data from related parasites of birds or reptiles are required. -
The Evolutionary Host Switches of Polychromophilus: a Multi-Gene
Witsenburg et al. Malaria Journal 2012, 11:53 http://www.malariajournal.com/content/11/1/53 RESEARCH Open Access The evolutionary host switches of Polychromophilus: a multi-gene phylogeny of the bat malaria genus suggests a second invasion of mammals by a haemosporidian parasite Fardo Witsenburg1*, Nicolas Salamin1,2 and Philippe Christe1 Abstract Background: The majority of Haemosporida species infect birds or reptiles, but many important genera, including Plasmodium, infect mammals. Dipteran vectors shared by avian, reptilian and mammalian Haemosporida, suggest multiple invasions of Mammalia during haemosporidian evolution; yet, phylogenetic analyses have detected only a single invasion event. Until now, several important mammal-infecting genera have been absent in these analyses. This study focuses on the evolutionary origin of Polychromophilus, a unique malaria genus that only infects bats (Microchiroptera) and is transmitted by bat flies (Nycteribiidae). Methods: Two species of Polychromophilus were obtained from wild bats caught in Switzerland. These were molecularly characterized using four genes (asl, clpc, coI, cytb) from the three different genomes (nucleus, apicoplast, mitochondrion). These data were then combined with data of 60 taxa of Haemosporida available in GenBank. Bayesian inference, maximum likelihood and a range of rooting methods were used to test specific hypotheses concerning the phylogenetic relationships between Polychromophilus and the other haemosporidian genera. Results: The Polychromophilus melanipherus and Polychromophilus murinus samples show genetically distinct patterns and group according to species. The Bayesian tree topology suggests that the monophyletic clade of Polychromophilus falls within the avian/saurian clade of Plasmodium and directed hypothesis testing confirms the Plasmodium origin. Conclusion: Polychromophilus’ ancestor was most likely a bird- or reptile-infecting Plasmodium before it switched to bats. -
First Molecular Detection of Polychromophilus Parasites in Brazilian Bat Species
microorganisms Article First Molecular Detection of Polychromophilus Parasites in Brazilian Bat Species Guilherme Augusto Minozzo 1,† , Bruno da Silva Mathias 2,† , Irina Nastassja Riediger 1, Lilian de Oliveira Guimarães 3 , Carolina Clares dos Anjos 2 , Eliana Ferreira Monteiro 2 , Andrea Pires dos Santos 4 , Alexander Welker Biondo 5 and Karin Kirchgatter 2,3,* 1 Laboratório Central de Saúde Pública do Paraná,São José dos Pinhais 83060-500, PR, Brazil; [email protected] (G.A.M.); [email protected] (I.N.R.) 2 Programa de Pós-Graduação em Medicina Tropical, Instituto de Medicina Tropical, Faculdade de Medicina, Universidade de São Paulo, São Paulo 05403-000, SP, Brazil; [email protected] (B.d.S.M.); [email protected] (C.C.d.A.); [email protected] (E.F.M.) 3 Laboratório de Bioquímica e Biologia Molecular, Superintendência de Controle de Endemias, São Paulo 01027-000b, SP, Brazil; [email protected] 4 Department of Comparative Pathobiology, Purdue University, West Lafayette, IN 47907, USA; [email protected] 5 Departamento de Medicina Veterinária, Universidade Federal do Paraná, Curitiba 80035-050, PR, Brazil; [email protected] * Correspondence: [email protected] † These authors contributed equally to this work. Abstract: Blood parasites of the Haemosporida order, such as the Plasmodium spp. responsible for Citation: Minozzo, G.A.; da Silva malaria, have become the focus of many studies in evolutionary biology. However, there is a lack of Mathias, B.; Riediger, I.N.; de Oliveira molecular investigation of haemosporidian parasites of wildlife, such as the genus Polychromophilus. Guimarães, L.; dos Anjos, C.C.; Species of this neglected genus exclusively have been described in bats, mainly in Europe, Asia, and Monteiro, E.F.; dos Santos, A.P.; Africa, but little is known about its presence and genetic diversity on the American continent. -
Publications Molecular Parasitology 2018 Aebischer A., Matuschewski K
Publications Molecular Parasitology 2018 Aebischer A., Matuschewski K., Hartmann S. (2018) Editorial: Parasite Infections: from experimental models to natural systems. Front. Cell. Infect. Microbiol. 8: 12. [Editorial] Arroyo-Olarte R.D., Thurow L., Kozjak-Pavlovic V., Gupta N. (2018). Illuminating pathogen-host intimacy through optogenetics. PLoS Pathog. 14: e1007046. [Review] Braun K., Stach T. Morphology and evolution of the central nervous system in adult tunicates. J. Zool. Syst Evol. Res., in press. Braun K., Stach T. (2018) Distribution and evolution of serotonin-like immunoreactive cells in Thaliacea (Tunicata). Zoomorphology 137: 565-578. Erler H., Ren B., Gupta N., Beitz E. (2018) The intracellular parasite Toxoplasma gondii harbors three druggable FNT-type formate and L-lactate transporters in the plasma membrane. J. Biol. Chem. 293, 17622-17630. Galen S.C., Borner J., Martinsen E.S., Schaer J., Austin C.C., West C.J., Perkins S.L. (2018) The polyphyly of Plasmodium: comprehensive phylogenetic analyses of the malaria parasites (order Haemosporida) reveal widespread taxonomic conflict. R. Soc. Open Sci. 5: 171780. Hillebrand A., Matz J.M., Almendinger M., Müller K., Matuschewski K., Schmitz-Linneweber C. (2018) Identification of clustered organelle short (cos) RNAs and of a conserved family of organellar RNA-binding proteins, the heptatricopeptide repeat proteins, in the malaria parasite. Nucleic Acids Res. 46: 10417- 10431. Huang G., Zhang S., Zhou C., Tang X., Li C., Wang C., Tang X., Suo J., Jia Y., El-Ashram S., Yu Z., Cai J., Gupta N., Suo X., Liu X. (2018) Influence of Eimeria falciformis infection on gut microbiota and metabolic pathways in mice.