Development of Brugia Malayi in Mongolian Gerbils Previously Infected with 100 Third-Stage Larvae of Wuchereria Bancrofti
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The Functional Parasitic Worm Secretome: Mapping the Place of Onchocerca Volvulus Excretory Secretory Products
pathogens Review The Functional Parasitic Worm Secretome: Mapping the Place of Onchocerca volvulus Excretory Secretory Products Luc Vanhamme 1,*, Jacob Souopgui 1 , Stephen Ghogomu 2 and Ferdinand Ngale Njume 1,2 1 Department of Molecular Biology, Institute of Biology and Molecular Medicine, IBMM, Université Libre de Bruxelles, Rue des Professeurs Jeener et Brachet 12, 6041 Gosselies, Belgium; [email protected] (J.S.); [email protected] (F.N.N.) 2 Molecular and Cell Biology Laboratory, Biotechnology Unit, University of Buea, Buea P.O Box 63, Cameroon; [email protected] * Correspondence: [email protected] Received: 28 October 2020; Accepted: 18 November 2020; Published: 23 November 2020 Abstract: Nematodes constitute a very successful phylum, especially in terms of parasitism. Inside their mammalian hosts, parasitic nematodes mainly dwell in the digestive tract (geohelminths) or in the vascular system (filariae). One of their main characteristics is their long sojourn inside the body where they are accessible to the immune system. Several strategies are used by parasites in order to counteract the immune attacks. One of them is the expression of molecules interfering with the function of the immune system. Excretory-secretory products (ESPs) pertain to this category. This is, however, not their only biological function, as they seem also involved in other mechanisms such as pathogenicity or parasitic cycle (molting, for example). Wewill mainly focus on filariae ESPs with an emphasis on data available regarding Onchocerca volvulus, but we will also refer to a few relevant/illustrative examples related to other worm categories when necessary (geohelminth nematodes, trematodes or cestodes). -
"Structure, Function and Evolution of the Nematode Genome"
Structure, Function and Advanced article Evolution of The Article Contents . Introduction Nematode Genome . Main Text Online posting date: 15th February 2013 Christian Ro¨delsperger, Max Planck Institute for Developmental Biology, Tuebingen, Germany Adrian Streit, Max Planck Institute for Developmental Biology, Tuebingen, Germany Ralf J Sommer, Max Planck Institute for Developmental Biology, Tuebingen, Germany In the past few years, an increasing number of draft gen- numerous variations. In some instances, multiple alter- ome sequences of multiple free-living and parasitic native forms for particular developmental stages exist, nematodes have been published. Although nematode most notably dauer juveniles, an alternative third juvenile genomes vary in size within an order of magnitude, com- stage capable of surviving long periods of starvation and other adverse conditions. Some or all stages can be para- pared with mammalian genomes, they are all very small. sitic (Anderson, 2000; Community; Eckert et al., 2005; Nevertheless, nematodes possess only marginally fewer Riddle et al., 1997). The minimal generation times and the genes than mammals do. Nematode genomes are very life expectancies vary greatly among nematodes and range compact and therefore form a highly attractive system for from a few days to several years. comparative studies of genome structure and evolution. Among the nematodes, numerous parasites of plants and Strikingly, approximately one-third of the genes in every animals, including man are of great medical and economic sequenced nematode genome has no recognisable importance (Lee, 2002). From phylogenetic analyses, it can homologues outside their genus. One observes high rates be concluded that parasitic life styles evolved at least seven of gene losses and gains, among them numerous examples times independently within the nematodes (four times with of gene acquisition by horizontal gene transfer. -
Molecular Phylogenetic Studies of the Genus Brugia Hong Xie Yale Medical School
Smith ScholarWorks Biological Sciences: Faculty Publications Biological Sciences 1994 Molecular Phylogenetic Studies of the Genus Brugia Hong Xie Yale Medical School O. Bain Biologie Parasitaire, Protistologie, Helminthologie, Museum d’Histoire Naturelle Steven A. Williams Smith College, [email protected] Follow this and additional works at: https://scholarworks.smith.edu/bio_facpubs Part of the Biology Commons Recommended Citation Xie, Hong; Bain, O.; and Williams, Steven A., "Molecular Phylogenetic Studies of the Genus Brugia" (1994). Biological Sciences: Faculty Publications, Smith College, Northampton, MA. https://scholarworks.smith.edu/bio_facpubs/37 This Article has been accepted for inclusion in Biological Sciences: Faculty Publications by an authorized administrator of Smith ScholarWorks. For more information, please contact [email protected] Article available at http://www.parasite-journal.org or http://dx.doi.org/10.1051/parasite/1994013255 MOLECULAR PHYLOGENETIC STUDIES ON BRUGIA FILARIAE USING HHA I REPEAT SEQUENCES XIE H.*, BAIN 0.** and WILLIAMS S. A.*,*** Summary : Résumé : ETUDES PHYLOGÉNÉTIQUES MOLÉCULAIRES DES FILAIRES DU GENRE BRUGIA À L'AIDE DE: LA SÉQUENCE RÉPÉTÉE HHA I This paper is the first molecular phylogenetic study on Brugia para• sites (family Onchocercidae) which includes 6 of the 10 species Cet article est la première étude plylogénétique moléculaire sur les of this genus : B. beaveri Ash et Little, 1964; B. buckleyi filaires du genre Brugia (Onchocercidae); elle inclut six des 10 Dissanaike et Paramananthan, 1961 ; B. malayi (Brug,1927) espèces du genre : B. beaveri Ash et Little, 1964; B. buckleyi Buckley, 1960 ; B. pohangi, (Buckley et Edeson, 1956) Buckley, Dissanaike et Paramananthan, 1961; B. malayi (Brug, 1927) 1960; B. patei (Buckley, Nelson et Heisch,1958) Buckley, 1960 Buckley, 1960; B. -
Filarial Genomics Steven A
Smith ScholarWorks Biological Sciences: Faculty Publications Biological Sciences 11-2004 Filarial Genomics Steven A. Williams Smith College, [email protected] Follow this and additional works at: https://scholarworks.smith.edu/bio_facpubs Part of the Biology Commons Recommended Citation Williams, Steven A., "Filarial Genomics" (2004). Biological Sciences: Faculty Publications, Smith College, Northampton, MA. https://scholarworks.smith.edu/bio_facpubs/45 This Article has been accepted for inclusion in Biological Sciences: Faculty Publications by an authorized administrator of Smith ScholarWorks. For more information, please contact [email protected] GLOBAL PROGRAM TO ELIMINATE LF 37 3.3 FILARIAL GENOMICS Steven A. Williams Summary of Prioritized Research Needs but few genes were cloned and identified. By the end of 1994, only 60 Brugia genes had been submitted to the Genbank 1) Collecting materials database. It was clear that a new approach for studying the a) Before the opportunity is lost to preserve their ge- filarial genome was needed to make rapid progress in under- nomes, collect geographically representative isolates of standing the biology and biochemistry of these parasites. The the various species and strains of the human filarial genome project approach represented a complete departure parasites, from the way parasite genes had been studied in the past. 2) Constructing libraries Genome projects are typically not directed at the identifica- a) Construct updated and additional genomic and cDNA tion of individual genes, but instead at the identification, clon- libraries to represent completely the different stages ing, and sequencing of all the organism’s genes. and species of filarial parasites, At the first meeting of the Filarial Genome Project (1994), 3) Sequencing B. -
Genomics of Loa Loa, a Wolbachia-Free Filarial Parasite of Humans
ARTICLES OPEN Genomics of Loa loa, a Wolbachia-free filarial parasite of humans Christopher A Desjardins1, Gustavo C Cerqueira1, Jonathan M Goldberg1, Julie C Dunning Hotopp2, Brian J Haas1, Jeremy Zucker1, José M C Ribeiro3, Sakina Saif1, Joshua Z Levin1, Lin Fan1, Qiandong Zeng1, Carsten Russ1, Jennifer R Wortman1, Doran L Fink4,5, Bruce W Birren1 & Thomas B Nutman4 Loa loa, the African eyeworm, is a major filarial pathogen of humans. Unlike most filariae, L. loa does not contain the obligate intracellular Wolbachia endosymbiont. We describe the 91.4-Mb genome of L. loa and that of the related filarial parasite Wuchereria bancrofti and predict 14,907 L. loa genes on the basis of microfilarial RNA sequencing. By comparing these genomes to that of another filarial parasite, Brugia malayi, and to those of several other nematodes, we demonstrate synteny among filariae but not with nonparasitic nematodes. The L. loa genome encodes many immunologically relevant genes, as well as protein kinases targeted by drugs currently approved for use in humans. Despite lacking Wolbachia, L. loa shows no new metabolic synthesis or transport capabilities compared to other filariae. These results suggest that the role of Wolbachia in filarial biology is more subtle All rights reserved. than previously thought and reveal marked differences between parasitic and nonparasitic nematodes. Filarial nematodes dwell within the lymphatics and subcutaneous (but not the worm itself) have shown efficacy in treating humans tissues of up to 170 million people worldwide and are responsible with these infections4,5. Through genomic analysis, Wolbachia have for notable morbidity, disability and socioeconomic loss1. -
Identification of Protective Immune Responses and the Immunomodulatory Capacity of Litomosoides Sigmodontis
Identification of protective immune responses and the immunomodulatory capacity of Litomosoides sigmodontis Dissertation zur Erlangung des Doktorgrades (Dr. rer. nat.) der Mathematisch-Naturwissenschaftlichen Fakultät der Rheinischen Friedrich-Wilhelms-Universität Bonn vorgelegt von JESUTHAS AJENDRA aus Dillingen/Saar Bonn 2016 i Angefertigt mit Genehmigung der Mathematisch-Naturwissenschaftlichen Fakultät der Rheinischen Friedrich-Wilhelms-Universität Bonn 1. Gutachter: Prof. Dr. Achim Hörauf 2. Gutachter: Prof. Dr. Waldemar Kolanus Tag der Promotion: 25.08.2016 ii Erscheinungsjahr: 2016 Erklärung Die hier vorgelegte Dissertation habe ich eigenständig und ohne unerlaubte Hilfsmittel angefertigt. Die Dissertation wurde in der vorgelegten oder in ähnlicher Form noch bei keiner anderen Institution eingereicht. Es wurden keine vorherigen oder erfolglosen Promotionsversuche unternommen. Bonn, 23.03.2016 Teile dieser Arbeit wurden vorab veröffentlicht in folgenden Publikationen: “ST2 deficiency does not impair type 2 immune responses during chronic filarial infection but leads to an increased microfilaremia due to an impaired splenic microfilarial clearance.” Ajendra J, Specht S, Neumann AL, Gondorf F, Schmidt D, Gentil K, Hoffmann WH, Taylor MJ, Hoerauf A, Hübner MP. PLoS One. 2014 Mar 24;9(3):e93072. doi: 10.1371/journal.pone.0093072. eCollection 2014. “Development of patent Litomosoides sigmodontis infections in semi-susceptible C57BL/6 mice in the absence of adaptive immune responses.” Layland LE, Ajendra J, Ritter M, Wiszniewsky A, Hoerauf A, Hübner MP. Parasit Vectors. 2015 Jul 25;8:396. doi: 10.1186/s13071-015-1011-2. “Combination of worm antigen and proinsulin prevents type 1 diabetes in NOD mice after the onset of insulitis.” Ajendra J, Berbudi A, Hoerauf A, Hübner MP. Clin Immunol. 2016 Feb 16; 164:119- 122. -
DNA of Brugia Malayi Detected in Several Mosquito Species Collected from Balangan District, South Borneo Province, Indonesia
Veterinary World, EISSN: 2231-0916 RESEARCH ARTICLE Available at www.veterinaryworld.org/Vol.13/May-2020/24.pdf Open Access DNA of Brugia malayi detected in several mosquito species collected from Balangan District, South Borneo Province, Indonesia Supriyono Supriyono1 and Suriyani Tan2 1. Division of Parasitology and Medical Entomology, Faculty of Veterinary Medicine, IPB University, Bogor 16680, West Java, Indonesia; 2. Department of Parasitology, Faculty of Medicine, Trisakti University, Jakarta, Indonesia. Corresponding author: Suriyani Tan, e-mail: [email protected] Co-author: SS: [email protected] Received: 17-01-2020, Accepted: 21-04-2020, Published online: 30-05-2020 doi: www.doi.org/10.14202/vetworld.2020.996-1000 How to cite this article: Supriyono S, Tan S (2020) DNA of Brugia malayi detected in several mosquito species collected from Balangan District, South Borneo Province, Indonesia, Veterinary World, 13(5): 996-1000. Abstract Background and Aim: Lymphatic filariasis (LF) is a lesser-known parasitic disease, which contributes to significant decreases in overall health. This study investigated the presence of Brugia malayi in mosquitoes collected in the South Borneo Province, Indonesia. Materials and Methods: Mosquitoes were collected through bare leg collection methods after sunset in several areas of the Hukai and Gulinggang villages in the Balangan District. The collected mosquitoes were identified based on morphological features and dissected to find microfilaria and then pooled through species for polymerase chain reaction (PCR) microfilaria detection. Results: A total of 837 female mosquitoes consisting of at least 14 species were selected; they were dissected, and no microfilariae were found. Mosquitoes were divided into 69 pools for PCR analysis. -
Host Plant Preference of Mansonia Mosquitoes
J. Aquat. Plant Manage. 44: 142-144 Host Plant Preference of Mansonia Mosquitoes GOUTAM CHANDRA1, A. GHOSH, D. BISWAS1 AND S. N. CHATTERJEE1 INTRODUCTION Mansonioides were obtained from a laboratory colony main- tained in the Mosquito Research Unit, Department of. Zool- Human brugian filariasis, which is caused by Brugia malayi ogy, The University of Burdwan. The colony was maintained and B. timori, affects 13 million people in the oriental region at 25 to 30°C, a pH of 6.95 to 7.03 and dissolved oxygen from (WHO 2002) and is most common in India and China (Otte- 5.5 to 6.1 mg/l in the laboratory and was kept free from ex- sen et al. 1997). The most important vectors of B. malayi, in posure to pathogens, insecticides, or repellents. Mosquito the endemic countries of South-east Asia, are different Man- larvae were fed on a fine-ground dog biscuit. The adult colo- sonia species in the subgenus Mansonioides. The vectors of the ny was provided with 10% sucrose and 10% multivitamin syr- parasite causing brugian filariasis in the Western Pacific and up, and was periodically blood-fed on restrained rats. South-east Asian regions were reviewed by Chow in 1973 and During the lab based experiment, pond water (500 ml) Ramaliangam in 1975, while Ma. annulifera was reported by was placed in each of 5 enamel bowls (bowl No. 1-5). Pond Iyengar in 1938, as an agent for transmission of B. malayi in water was sieved through a net (>500 mesh) to exclude lar- Travancore, India. -
Investigations of Filarial Nematode Motility, Response to Drug Treatment, and Pathology
Western Michigan University ScholarWorks at WMU Dissertations Graduate College 8-2015 Investigations of Filarial Nematode Motility, Response to Drug Treatment, and Pathology Charles Nutting Western Michigan University, [email protected] Follow this and additional works at: https://scholarworks.wmich.edu/dissertations Part of the Biochemistry Commons, Biology Commons, and the Pathogenic Microbiology Commons Recommended Citation Nutting, Charles, "Investigations of Filarial Nematode Motility, Response to Drug Treatment, and Pathology" (2015). Dissertations. 745. https://scholarworks.wmich.edu/dissertations/745 This Dissertation-Open Access is brought to you for free and open access by the Graduate College at ScholarWorks at WMU. It has been accepted for inclusion in Dissertations by an authorized administrator of ScholarWorks at WMU. For more information, please contact [email protected]. INVESTIGATIONS OF FILARIAL NEMATODE MOTILITY, RESPONSE TO DRUG TREATMENT, AND PATHOLOGY by Charles S. Nutting A dissertation submitted to the Graduate College in partial fulfillment of the requirements for the degree of Doctor of Philosophy Biological Sciences Western Michigan University August 2015 Doctoral Committee: Rob Eversole, Ph.D., Chair Charles Mackenzie, Ph.D. Pamela Hoppe, Ph.D. Charles Ide, Ph.D. INVESTIGATIONS OF FILARIAL NEMATODE MOTILITY, RESPONSE TO DRUG TREATMENT, AND PATHOLOGY Charles S. Nutting, Ph.D. Western Michigan University, 2015 More than a billion people live at risk of chronic diseases caused by parasitic filarial nematodes. These diseases: lymphatic filariasis, onchocerciasis, and loaisis cause significant morbidity, degrading the health, quality of life, and economic productivity of those who suffer from them. Though treatable, there is no cure to rid those infected of adult parasites. The parasites can modulate the immune system and live for 10-15 years. -
PDF 290 Kb) Roberts Et Al
Uni et al. Parasites & Vectors (2017) 10:194 DOI 10.1186/s13071-017-2105-9 RESEARCH Open Access Morphological and molecular characteristics of Malayfilaria sofiani Uni, Mat Udin & Takaoka n. g., n. sp. (Nematoda: Filarioidea) from the common treeshrew Tupaia glis Diard & Duvaucel (Mammalia: Scandentia) in Peninsular Malaysia Shigehiko Uni1,2*, Ahmad Syihan Mat Udin1, Takeshi Agatsuma3, Weerachai Saijuntha3,4, Kerstin Junker5, Rosli Ramli1, Hasmahzaiti Omar1, Yvonne Ai-Lian Lim6, Sinnadurai Sivanandam6, Emilie Lefoulon7, Coralie Martin7, Daicus Martin Belabut1, Saharul Kasim1, Muhammad Rasul Abdullah Halim1, Nur Afiqah Zainuri1, Subha Bhassu1, Masako Fukuda8, Makoto Matsubayashi9, Masashi Harada10, Van Lun Low11, Chee Dhang Chen1, Narifumi Suganuma3, Rosli Hashim1, Hiroyuki Takaoka1 and Mohd Sofian Azirun1 Abstract Background: The filarial nematodes Wuchereria bancrofti (Cobbold, 1877), Brugia malayi (Brug, 1927) and B. timori Partono, Purnomo, Dennis, Atmosoedjono, Oemijati & Cross, 1977 cause lymphatic diseases in humans in the tropics, while B. pahangi (Buckley & Edeson, 1956) infects carnivores and causes zoonotic diseases in humans in Malaysia. Wuchereria bancrofti, W. kalimantani Palmieri, Pulnomo, Dennis & Marwoto, 1980 and six out of ten Brugia spp. have been described from Australia, Southeast Asia, Sri Lanka and India. However, the origin and evolution of the species in the Wuchereria-Brugia clade remain unclear. While investigating the diversity of filarial parasites in Malaysia, we discovered an undescribed species in the common treeshrew Tupaia glis Diard & Duvaucel (Mammalia: Scandentia). Methods: We examined 81 common treeshrews from 14 areas in nine states and the Federal Territory of Peninsular Malaysia for filarial parasites. Once any filariae that were found had been isolated, we examined their morphological characteristics and determined the partial sequences of their mitochondrial cytochrome c oxidase subunit 1 (cox1) and 12S rRNA genes. -
Brugia Rapid
v.1.0 (November 2012) Brugia Rapid Test for diagnosis of Brugian filariasis The Brugia Rapid test has been shown to be a useful and sensitive tool for the detection of Brugia malayi and Brugia timori antibodies and is being used widely by lymphatic filariasis elimination programs in Brugia spp. endemic areas. Although the test is relatively simple to use, adequate training is necessary to reduce inter- observer variability and to reduce the misreading of cassettes. Basic Guidelines i. Cassettes are currently known to have a limited shelf life at ambient temperatures (18 months at 25°C) but longer shelf life when stored at 4°C (approximately 24 months). Cassettes and buffer solution should NOT be frozen. ii. Thirty-five microliters of blood should be collected by finger prick into a calibrated capillary tube coated with an anticoagulant (EDTA or heparin). Alternatively, finger prick blood can be collected into a microcentrifuge blood collection tube coated with either EDTA or heparin. iii. Although not required, transporting cassettes for use in the field in a cool box is recommended. Care should be taken not to expose cassettes to extreme heat for prolonged periods of time. iv. Cassettes must be read using adequate lighting. Faint lines can be difficult to see when lighting is not adequate. Test Procedure 1 Bring test cassette and chase buffer to room temperature. Remove cassette from foil pouch just prior to use. Label the cassette with sample information. Collect 35µL blood by finger prick using a calibrated capillary tube OR 2 measure 35µL of blood from a microcentrifuge tube using a micropipettor. -
A Transcriptomic Analysis of the Phylum Nematoda
There are amendments to this paper ARTICLES A transcriptomic analysis of the phylum Nematoda John Parkinson1,2, Makedonka Mitreva3, Claire Whitton2, Marian Thomson2, Jennifer Daub2, John Martin3, Ralf Schmid2, Neil Hall4,6, Bart Barrell4, Robert H Waterston3,6, James P McCarter3,5 & Mark L Blaxter2 The phylum Nematoda occupies a huge range of ecological niches, from free-living microbivores to human parasites. We analyzed the genomic biology of the phylum using 265,494 expressed-sequence tag sequences, corresponding to 93,645 putative genes, from 30 species, including 28 parasites. From 35% to 70% of each species’ genes had significant similarity to proteins from the model nematode Caenorhabditis elegans. More than half of the putative genes were unique to the phylum, and 23% were unique to the species from which they were derived. We have not yet come close to exhausting the genomic diversity of the phylum. We identified more than 2,600 different known protein domains, some of which had differential abundances between major taxonomic groups of nematodes. We also defined 4,228 nematode-specific protein families from nematode-restricted genes: http://www.nature.com/naturegenetics this class of genes probably underpins species- and higher-level taxonomic disparity. Nematode-specific families are particularly interesting as drug and vaccine targets. Nematodes, or roundworms, are a highly diverse group of organisms1. Much of what we know about the molecular and developmental What nematodes lack in obvious morphological disparity, they make biology of nematodes stems from the study of the free-living soil up for in abundance, accounting for 80% of all individual animals on rhabditine nematode Caenorhabditis elegans (Fig.