Miscellaneous Ways to Repel, Treat and Avoid Being Bitten by Sand Flies (Diptera: Pschodidae: Phlebotominae) on Human
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Vectorborne Transmission of Leishmania Infantum from Hounds, United States
Vectorborne Transmission of Leishmania infantum from Hounds, United States Robert G. Schaut, Maricela Robles-Murguia, and Missouri (total range 21 states) (12). During 2010–2013, Rachel Juelsgaard, Kevin J. Esch, we assessed whether L. infantum circulating among hunting Lyric C. Bartholomay, Marcelo Ramalho-Ortigao, dogs in the United States can fully develop within sandflies Christine A. Petersen and be transmitted to a susceptible vertebrate host. Leishmaniasis is a zoonotic disease caused by predomi- The Study nantly vectorborne Leishmania spp. In the United States, A total of 300 laboratory-reared female Lu. longipalpis canine visceral leishmaniasis is common among hounds, sandflies were allowed to feed on 2 hounds naturally in- and L. infantum vertical transmission among hounds has been confirmed. We found thatL. infantum from hounds re- fected with L. infantum, strain MCAN/US/2001/FOXY- mains infective in sandflies, underscoring the risk for human MO1 or a closely related strain. During 2007–2011, the exposure by vectorborne transmission. hounds had been tested for infection with Leishmania spp. by ELISA, PCR, and Dual Path Platform Test (Chembio Diagnostic Systems, Inc. Medford, NY, USA (Table 1). L. eishmaniasis is endemic to 98 countries (1). Canids are infantum development in these sandflies was assessed by Lthe reservoir for zoonotic human visceral leishmani- dissecting flies starting at 72 hours after feeding and every asis (VL) (2), and canine VL was detected in the United other day thereafter. Migration and attachment of parasites States in 1980 (3). Subsequent investigation demonstrated to the stomodeal valve of the sandfly and formation of a that many US hounds were infected with Leishmania infan- gel-like plug were evident at 10 days after feeding (Figure tum (4). -
5226.Full.Pdf
Sandfly Maxadilan Exacerbates Infection with Leishmania major and Vaccinating Against It Protects Against L. major Infection This information is current as Robin V. Morris, Charles B. Shoemaker, John R. David, of October 2, 2021. Gregory C. Lanzaro and Richard G. Titus J Immunol 2001; 167:5226-5230; ; doi: 10.4049/jimmunol.167.9.5226 http://www.jimmunol.org/content/167/9/5226 Downloaded from References This article cites 36 articles, 20 of which you can access for free at: http://www.jimmunol.org/content/167/9/5226.full#ref-list-1 http://www.jimmunol.org/ Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication *average by guest on October 2, 2021 Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2001 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. Sandfly Maxadilan Exacerbates Infection with Leishmania major and Vaccinating Against It Protects Against L. major Infection1 Robin V. Morris,* Charles B. Shoemaker,† John R. David,† Gregory C. Lanzaro,‡ and Richard G. Titus2* Bloodfeeding arthropods transmit many of the world’s most serious infectious diseases. -
Stuck in The
WNV entry to the brain. This was confirmed by comparing the per- meability of the BBB in wild-type and Tlr3–/– mice: following WNV infection or stimulation with the viral mimic poly (I:C), the perme- ability was increased in wild-type mice but not in Tlr3–/– mice. A fur- ther insight into the pathogenesis of severe disease was provided by results suggesting that TNF-α receptor 1 signalling downstream of Tlr3 promotes WNV entry into the A female sandfly (Phlebotomus species), which is the vector of Leishmania major. The females are blood suckers and transmit parasites to humans. brain. Image courtesy of the WHO © (1975). Sporadic outbreaks of WNV infection of humans have become PARASITOLOGY increasingly common over the past 5 years, particularly in North America and Europe. This new work identifying Tlr3 as the receptor Stuck in the gut allowing WNV to enter the brain can hopefully be exploited for the Cutaneous leishmaniasis, caused by infection with papatasi and identified a galactose-binding protein development of new therapeutics. Leishmania major,is the most common Old World named PpGalec. PpGalec is a tandem-repeat Sheilagh Molloy leishmanial disease and is transmitted by the galectin with two CRDs separated by a linker and sandfly. To devise new methods of parasite control it was specifically expressed in the midgut and References and links is imperative to understand the biology of infection upregulated in adult females. Moreover, PpGalec ORIGINAL RESEARCH PAPER Wang, T. et al. Toll-like receptor 3 mediates West Nile virus entry in both the host and the vector. In a recent report in was only found in P. -
Top Tips How to Avoid Vector Borne Diseases (Eng)
Tr a a v r e i ljl s k in a g r e to a Vectors such as mosquitoes, sandflies and HOW tO AvOid ticks can transmit serious infectious diseases both in vEctOR-BORnE the WHO European Region disEAsEs – tOp tips and globally. Many of these vectors are blood sucking and transfer diseases to Take simple measures to protect yourself and your family. human beings through their bites. 1. Before you travel, be vaccinated against diseases prevalent at your destination. vaccines exist for yellow fever, Japanese encephalitis and tick- Avoid being bitten by a borne encephalitis. mosquito, sandfly or tick. 2. consult your doctor, 4–6 weeks before departure if possible, to discuss how you can protect yourself (for example, what antimalarial medicines you Be prepared. should take if malaria is endemic at your destination). 3. Wear light-coloured, long-sleeved shirts and long trousers, tucked into socks or boots, and use insect repellent on exposed skin and clothing to protect yourself from being bitten by mosquitoes, sandflies or ticks. temperature, humidity and the time of day affect the likelihood of being bitten, so know when you need extra protective clothing and insect repellent. 4. Use window screens, if available, to keep mosquitoes outside the place where you are staying. 5. sleep under an insecticide-treated bed net, requesting one if necessary, if you are staying in an area with malaria risk. 6. check your body regularly for ticks. if you find one, remove it with tweezers and apply a skin disinfectant. in tick-infested areas, examine your clothing, luggage and other belongings thoroughly before entering the place where you are staying. -
Comprehensive Guidelines for Prevention and Control of Dengue and Dengue Haemorrhagic Fever
C o m p r e h e n s Dengue fever (DF) is the fastest emerging arboviral infection spread by Aedes aegypti i v mosquitoes with major public health consequences for millions of people around the e G world, and in particular the South-East Asia and Asia-Pacific Regions of the World u i Health Organization (WHO). Of the 2.5 billion people globally at risk of DF and its d e severe forms dengue haemorrhagic fever (DHF) and dengue shock syndrome (DSS) l i n South-East Asia accounts for approximately 1.3 billion or 52%. e s f As the disease spreads to new geographical areas, the frequency of the o r outbreaks has increased along with a rapidly changing disease epidemiology. In P r response to resolution of the Forty-sixth World Health Assembly urging Member e v States to strengthen national programmes for control of DF/DHF, several documents e n were developed by regional offices of WHO, including South-East Asia. t i o In 1999 the WHO Regional Office for South-East Asia published the Regional n a Comprehensive Guidelines for Guidelines for the Prevention and Control of DF/DHF. Since then new strategies and n d developments in the control of dengue fever, DHF and DSS have come to light. The C Regional Guidelines were extensively revised, updated and expanded with the focus o n Prevention and Control of on new and additional topics of current relevance to the populations of Member t r o States of the Region. They were then rechristened the Comprehensive Guidelines for l o the Prevention and Control of Dengue and Dengue Haemmorhagic Fever. -
Guide Yellow Fever Outbreak 2016
© World Health Organization 2016 All rights reserved. Publications of the World Health Organization are available on the WHO website (www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications –whether for sale or for non-commercial distribution– should be addressed to WHO Press through the WHO website (www.who.int/about/licensing/copyright_form/en/index.html). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader. -
Leishmania Species
APPENDIX 2 Leishmania Species • Fewer than 15 probable or confirmed cases of trans- mission by blood transfusion and 10 reported cases of Disease Agent: congenital transmission worldwide • Leishmania species At-Risk Populations: Disease Agent Characteristics: • Residents of and travelers to endemic areas Vector and Reservoir Involved: • Protozoan, 2.5 ¥ 5.0 mm • Order: Kinetoplastida • Phlebotomine sandflies: Phlebotomus genus (Old • Family: Trypanosomatidae World) and Lutzomyia genus (New World) • Intracellular pathogen of macrophages/monocytes • Only the amastigote stage is found in humans. Blood Phase: • Leishmania parasites survive and multiply in mono- Disease Name: nuclear phagocytes. Parasite circulation in peripheral • Leishmaniasis blood has been reported in asymptomatic L. dono- • Visceral leishmaniasis is called kala-azar in India and vani, L. tropica, and L. infantum infections, and in various names elsewhere. treated and inapparent L. braziliensis infections. • Cutaneous forms have a variety of colloquial names Survival/Persistence in Blood Products: around the world. • Leishmania species are known to survive in human Priority Level: RBCs under blood bank storage conditions for as long as 15 days and longer in experimental animal models. • Scientific/Epidemiologic evidence regarding blood safety: Low Transmission by Blood Transfusion: • Public perception and/or regulatory concern regard- ing blood safety: Low • Transfusion transmission has been documented in at • Public concern regarding disease agent: Low, but least three cases -
How Can We Use Genetic Engineering to Get Rid of Malaria for Good?
DECEMBERMARCH 20172020 How can we use genetic engineering to get rid of malaria for good? Authors: Susan Crow, Meghan Pawlowski, Manyowa Meki, LaraAuthors: LaDage, Timothy Roth II, Cynthia Downs, BarryKyros SinervoKyrou, Andrew and Vladimir Hammond, Pravosudov Andrea Crisanti & others Associate Editors: LindseySeda Dawson Hall and and Gogi Madeleine Kalka Corcoran Abstract Nobody likes the buzzing sound or itchy bite of mosquitoes. What if we used genetic engineering? Here we modified But mosquito bites (only females bite, by the way!) are not the genetic makeup of Anopheles gambiae mosquitoes (the just irritating: they can carry and spread deadly diseases main carriers of malaria). The mutation prevented females such as malaria, dengue, yellow fever and many more. Every from biting and laying eggs. It spread through our caged year, millions of people die from mosquito-borne diseases and populations quickly and drove them extinct. Our results pave most of them are young children. There are ways to get rid the way for lowering mosquito populations in the wild and of mosquitoes and prevent such diseases, but they are not as getting rid of malaria in the future. effective as we would like. EDITING GENES WITH CRISPR A tool used by scientists to precisely edit genes inside cells. Introduction It consists of two parts… Cas9 Guide RNA (An enzyme that (Directs the Cas9 You may have heard about malaria and the devastation it cuts DNA) + to the target DNA) causes in Africa. But did you know that a child dies of malaria every two minutes? Despite global efforts, malaria remains one of the world’s deadliest diseases. -
Best Management Practices for Mosquito Control ______
Best Management Practices for Mosquito Control ___________________________________________________ Washington State Department of Ecology Water Quality Program May 2004 Publication 03-10-023 revised Best Management Practices for Mosquito Control ___________________________________________________ Washington State Department of Ecology Water Quality Program May 2004 Publication 03-10-023 revised For additional copies of this document contact: Department of Ecology Publications Distribution Center P.O. Box 47600 Olympia, WA 98504-7600 Telephone: (360) 407-7472 Headquarters (Lacey) 360-407-6000 If you are speech or hearing impaired, call 711 or 1-800-833-6388 for TTY Re gional Whatcom Pend San Juan Office Oreille location Skagit Okanogan Stevens Island Northwest Central Ferry 425-649-7000 Clallam Snohomish 509-575-2490 Chelan Jefferson Spokane K Douglas i Bellevue Lincoln ts Spokane ap Grays King Eastern Harbor Mason Kittitas Grant 509-329-3400 Pierce Adams Lacey Whitman Thurston Southwest Pacific Lewis 360-407-6300 Yakima Franklin Garfield Wahkiakum Yakima Columbia Walla Cowlitz Benton Asotin Skamania Walla Klickitat Clark If you need this publication in an alternate format, please contact us at 360-407-6404. Call TTY (for the speech and hearing impaired) at 711 or 1-800-833-6388. Table of Contents Table of Contents...................................................................................................................i Tables ...................................................................................................................................ii -
Sandfly Lutzomyia Longipalpis in a Cutaneous Leishmaniasis Focus In
Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 91(4): 415-419, Jul./Aug. 1996 415 Sandfly Lutzomyia longipalpis in a Cutaneous Leishmaniasis Focus in Central Colombia Yolanda López+, Lisardo Osorio, Gilberto Alvarez, Jaime Rojas*, Fernando Jiménez*, Carmen Gómez*, Cristina Ferro** Grupo de Entomología, Laboratorio Departamental de Salud Pública, Dirección Seccional de Salud de Antioquia, Carrera 51A No 62-42, Medellín, Colombia *Servicio Seccional de Salud de Antioquia (Hospitales de Puerto Triunfo y Rionegro) **Laboratorio de Entomología, Instituto Nacional de Salud, Avenida el Dorado con Carrera 50, Santafé de Bogotá, Colombia Lutzomyia longipalpis, 15 other species of the genus Lutzomyia, and one species of Brumptomyia were collected in an endemic focus of cutaneous leishmaniasis in a river canyon 450 m above sea-level, in Rio Claro, Antioquia, Colombia. The presence of Lu. longipalpis is associated with the destruction of the primary forest and the development of new farmland and rural settlement in this region. The compo- sition of species identified a different habitat for Lu. longipalpis in Colombia. Lu. yuilli and Lu. longipalpis were predominant (68.26%) followed by Lu. trapidoi, Lu. hartmani, Lu. triramula, Lu. panamensis, Lu. gomezi. Key words: Lutzomyia longipalpis - sand fly - ecology - leishmaniasis - Colombia Lutzomyia longipalpis (Lutz & Neiva) is the perspective, this is one of the most important main vector of Leishmania (L.) chagasi, the emerging parasitic diseases (Tesh 1995). aetiologic agent of American visceral leishmaniasis In Colombia, the geographic distribution of (Ward 1985, Shaw & Lainson 1987, Momen et al. visceral leishmaniasis and Lu. longipalpis coincide 1987, Grimaldi et al. 1989, Cupolillo et al. 1994, in the upper and middle Magdalena River Valley, Tesh 1995). -
Insights Into Leishmania Molecules and Their Potential Contribution to the Virulence of the Parasite
veterinary sciences Review Insights into Leishmania Molecules and Their Potential Contribution to the Virulence of the Parasite Ehab Kotb Elmahallawy 1,* and Abdulsalam A. M. Alkhaldi 2,* 1 Department of Zoonoses, Faculty of Veterinary Medicine, Sohag University, Sohag 82524, Egypt 2 Biology Department, College of Science, Jouf University, Sakaka, Aljouf 2014, Saudi Arabia * Correspondence: [email protected] (E.K.E.); [email protected] (A.A.M.A.) Abstract: Neglected parasitic diseases affect millions of people worldwide, resulting in high mor- bidity and mortality. Among other parasitic diseases, leishmaniasis remains an important public health problem caused by the protozoa of the genus Leishmania, transmitted by the bite of the female sand fly. The disease has also been linked to tropical and subtropical regions, in addition to being an endemic disease in many areas around the world, including the Mediterranean basin and South America. Although recent years have witnessed marked advances in Leishmania-related research in various directions, many issues have yet to be elucidated. The intention of the present review is to give an overview of the major virulence factors contributing to the pathogenicity of the parasite. We aimed to provide a concise picture of the factors influencing the reaction of the parasite in its host that might help to develop novel chemotherapeutic and vaccine strategies. Keywords: Leishmania; parasite; virulence; factors Citation: Elmahallawy, E.K.; Alkhaldi, A.A.M. Insights into 1. Introduction Leishmania Molecules and Their Leishmaniasis is a group of neglected tropical diseases caused by an opportunistic Potential Contribution to the intracellular protozoan organism of the genus Leishmania that affects people, domestic Virulence of the Parasite. -
How Can We Use Genetic Engineering to Get Rid of Malaria for Good? Teacher’S Key
How can we use genetic engineering to get rid of malaria for good? TEACher’s key Check your understanding 1 Anopheles gambiae mosquitoes are a vector species for malaria. What is a vector species? Can you find out about some other vector species and the diseases they transmit? A vector is an organism that does not cause disease itself but which spreads infection by transmitting pathogens (virus, bacteria, parasites, etc.) from one host to another. Mosquitoes are vector species of many infectious diseases including malaria, dengue, yellow fever, Zika, and West Nile virus. Some other vector species are ticks (Lyme Answer disease), fleas (bubonic plague), raccoons, bats, foxes, skunks (rabies). Scientists genetically engineered Anopheles gambiae mosquitoes. What were the characteristics of engineered 2 mosquitoes that drove the lab populations to extinction? Male mosquitoes with one or both copies of the mutated gene had no physical differences but they were carriers of the mutated gene and passed it onto their offspring. Female mosquitoes with one copy of the mutated gene were healthy but they had reduced fertility. They passed the mutated gene on to the next generation. Females with two copies of the mutated gene had male body parts (a mouth that is not structured to bite, claspers, and hairy Answer antennae). Most importantly, they were infertile - they couldn’t lay eggs. So once all females carried two copies of the mutated gene, the population collapsed. 3 Scientists used a new approach that made this study so successful at wiping out mosquito populations: CRISPR/Cas9 gene drive. What is the purpose of a gene drive? How does it speed up the spread of a useful genetic mutation? In sexual reproduction, half of the genes come from the male organism and the other half come from the female organism.