Cat Flea, Ctenocephalides Felis (Bouché)1 D
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Species List 02/11/2017
1 of 27 Kelvingrove Park - species list 02/11/2017 Group Taxon Common Name Earliest Latest Records acarine Hydracarina 2004 2004 1 amphibian Bufo bufo Common Toad 2014 2014 2 amphibian Lissotriton helveticus Palmate Newt 2006 2006 1 amphibian Lissotriton vulgaris Smooth Newt 1997 1997 1 amphibian Rana temporaria Common Frog 2009 2017 6 annelid Alboglossiphonia heteroclita 2003 2004 2 annelid Erpobdella testacea 2003 2003 1 annelid Glossiphonia complanata 2003 2003 1 annelid Helobdella stagnalis 2003 2014 3 annelid Lumbricus terrestris Common Earthworm 1996 2000 1 annelid Naididae 2004 2004 1 annelid Tubificidae Tubificid Worm Sp. 2003 2004 2 bird Acanthis flammea Common (Mealy) Redpoll 1991 1991 1 bird Accipiter nisus Sparrowhawk 1983 2008 7 bird Aegithalos caudatus Long-tailed Tit 1991 2017 16 bird Aix galericulata Mandarin Duck 1969 1969 1 bird Alcedo atthis Kingfisher 1988 2017 27 bird Anas penelope Wigeon 1994 1994 1 bird Anas platyrhynchos Mallard 1968 2014 246 bird Anser anser Greylag Goose 1973 1973 1 bird Apus apus Swift 2008 2014 4 bird Ardea cinerea Grey Heron 1991 2014 28 bird Aythya ferina Pochard 1939 1994 10 bird Aythya fuligula Tufted Duck 1992 2004 16 bird Bucephala clangula Goldeneye 1991 2006 59 bird Carduelis carduelis Goldfinch 1998 2014 12 bird Certhia familiaris Treecreeper 1995 2017 11 bird Chloris chloris Greenfinch 1988 2016 7 bird Chroicocephalus ridibundus Black-headed Gull 1961 2014 16 bird Cinclus cinclus Dipper 1991 2014 8 bird Columba livia Feral Pigeon 1958 2015 21 bird Columba oenas Stock Dove 2014 2015 2 bird Columba palumbus Woodpigeon 2014 2014 7 bird Corvus corone Carrion Crow 2014 2014 1 2 of 27 Kelvingrove Park - species list 02/11/2017 Group Taxon Common Name Earliest Latest Records bird Corvus corone agg. -
Fleas, Hosts and Habitat: What Can We Predict About the Spread of Vector-Borne Zoonotic Diseases?
2010 Fleas, Hosts and Habitat: What can we predict about the spread of vector-borne zoonotic diseases? Ph.D. Dissertation Megan M. Friggens School of Forestry I I I \, l " FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? by Megan M. Friggens A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Forest Science Northern Arizona University May 2010 ?Jii@~-~-u-_- Robert R. Parmenter, Ph. D. ~",l(*~ l.~ Paulette L. Ford, Ph. D. --=z:r-J'l1jU~ David M. Wagner, Ph. D. ABSTRACT FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? MEGAN M. FRIGGENS Vector-borne diseases of humans and wildlife are experiencing resurgence across the globe. I examine the dynamics of flea borne diseases through a comparative analysis of flea literature and analyses of field data collected from three sites in New Mexico: The Sevilleta National Wildlife Refuge, the Sandia Mountains and the Valles Caldera National Preserve (VCNP). My objectives were to use these analyses to better predict and manage for the spread of diseases such as plague (Yersinia pestis). To assess the impact of anthropogenic disturbance on flea communities, I compiled and analyzed data from 63 published empirical studies. Anthropogenic disturbance is associated with conditions conducive to increased transmission of flea-borne diseases. Most measures of flea infestation increased with increasing disturbance or peaked at intermediate levels of disturbance. Future trends of habitat and climate change will probably favor the spread of flea-borne disease. -
Fleas and Flea-Borne Diseases
International Journal of Infectious Diseases 14 (2010) e667–e676 Contents lists available at ScienceDirect International Journal of Infectious Diseases journal homepage: www.elsevier.com/locate/ijid Review Fleas and flea-borne diseases Idir Bitam a, Katharina Dittmar b, Philippe Parola a, Michael F. Whiting c, Didier Raoult a,* a Unite´ de Recherche en Maladies Infectieuses Tropicales Emergentes, CNRS-IRD UMR 6236, Faculte´ de Me´decine, Universite´ de la Me´diterrane´e, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France b Department of Biological Sciences, SUNY at Buffalo, Buffalo, NY, USA c Department of Biology, Brigham Young University, Provo, Utah, USA ARTICLE INFO SUMMARY Article history: Flea-borne infections are emerging or re-emerging throughout the world, and their incidence is on the Received 3 February 2009 rise. Furthermore, their distribution and that of their vectors is shifting and expanding. This publication Received in revised form 2 June 2009 reviews general flea biology and the distribution of the flea-borne diseases of public health importance Accepted 4 November 2009 throughout the world, their principal flea vectors, and the extent of their public health burden. Such an Corresponding Editor: William Cameron, overall review is necessary to understand the importance of this group of infections and the resources Ottawa, Canada that must be allocated to their control by public health authorities to ensure their timely diagnosis and treatment. Keywords: ß 2010 International Society for Infectious Diseases. Published by Elsevier Ltd. All rights reserved. Flea Siphonaptera Plague Yersinia pestis Rickettsia Bartonella Introduction to 16 families and 238 genera have been described, but only a minority is synanthropic, that is they live in close association with The past decades have seen a dramatic change in the geographic humans (Table 1).4,5 and host ranges of many vector-borne pathogens, and their diseases. -
Arthropod Parasites in Domestic Animals
ARTHROPOD PARASITES IN DOMESTIC ANIMALS Abbreviations KINGDOM PHYLUM CLASS ORDER CODE Metazoa Arthropoda Insecta Siphonaptera INS:Sip Mallophaga INS:Mal Anoplura INS:Ano Diptera INS:Dip Arachnida Ixodida ARA:Ixo Mesostigmata ARA:Mes Prostigmata ARA:Pro Astigmata ARA:Ast Crustacea Pentastomata CRU:Pen References Ashford, R.W. & Crewe, W. 2003. The parasites of Homo sapiens: an annotated checklist of the protozoa, helminths and arthropods for which we are home. Taylor & Francis. Taylor, M.A., Coop, R.L. & Wall, R.L. 2007. Veterinary Parasitology. 3rd edition, Blackwell Pub. HOST-PARASITE CHECKLIST Class: MAMMALIA [mammals] Subclass: EUTHERIA [placental mammals] Order: PRIMATES [prosimians and simians] Suborder: SIMIAE [monkeys, apes, man] Family: HOMINIDAE [man] Homo sapiens Linnaeus, 1758 [man] ARA:Ast Sarcoptes bovis, ectoparasite (‘milker’s itch’)(mange mite) ARA:Ast Sarcoptes equi, ectoparasite (‘cavalryman’s itch’)(mange mite) ARA:Ast Sarcoptes scabiei, skin (mange mite) ARA:Ixo Ixodes cornuatus, ectoparasite (scrub tick) ARA:Ixo Ixodes holocyclus, ectoparasite (scrub tick, paralysis tick) ARA:Ixo Ornithodoros gurneyi, ectoparasite (kangaroo tick) ARA:Pro Cheyletiella blakei, ectoparasite (mite) ARA:Pro Cheyletiella parasitivorax, ectoparasite (rabbit fur mite) ARA:Pro Demodex brevis, sebacceous glands (mange mite) ARA:Pro Demodex folliculorum, hair follicles (mange mite) ARA:Pro Trombicula sarcina, ectoparasite (black soil itch mite) INS:Ano Pediculus capitis, ectoparasite (head louse) INS:Ano Pediculus humanus, ectoparasite (body -
Ctenocephalides Felis Infesting Outdoor Dogs in Spain Rosa Gálvez1, Vicenzo Musella2, Miguel A
Gálvez et al. Parasites & Vectors (2017) 10:428 DOI 10.1186/s13071-017-2357-4 RESEARCH Open Access Modelling the current distribution and predicted spread of the flea species Ctenocephalides felis infesting outdoor dogs in Spain Rosa Gálvez1, Vicenzo Musella2, Miguel A. Descalzo3, Ana Montoya1, Rocío Checa1, Valentina Marino1, Oihane Martín1, Giuseppe Cringoli4, Laura Rinaldi4 and Guadalupe Miró1* Abstract Background: The cat flea, Ctenocephalides felis, is the most prevalent flea species detected on dogs and cats in Europe and other world regions. The status of flea infestation today is an evident public health concern because of their cosmopolitan distribution and the flea-borne diseases transmission. This study determines the spatial distribution of the cat flea C. felis infesting dogs in Spain. Using geospatial tools, models were constructed based on entomological data collected from dogs during the period 2013–2015. Bioclimatic zones, covering broad climate and vegetation ranges, were surveyed in relation to their size. Results: The models builded were obtained by negative binomial regression of several environmental variables to show impacts on C. felis infestation prevalence: land cover, bioclimatic zone, mean summer and autumn temperature, mean summer rainfall, distance to urban settlement and normalized difference vegetation index. In the face of climate change, we also simulated the future distributions of C. felis for the global climate model (GCM) “GFDL-CM3” and for the representative concentration pathway RCP45, which predicts their spread in the country. Conclusions: Predictive models for current climate conditions indicated the widespread distribution of C. felis throughout Spain, mainly across the central northernmost zone of the mainland. Under predicted conditions of climate change, the risk of spread was slightly greater, especially in the north and central peninsula, than for the current situation. -
Zoonotic Diseases Associated with Free-Roaming Cats R
Zoonoses and Public Health REVIEW ARTICLE Zoonotic Diseases Associated with Free-Roaming Cats R. W. Gerhold1 and D. A. Jessup2 1 Center for Wildlife Health, Department of Forestry, Wildlife, and Fisheries, The University of Tennessee, Knoxville, TN, USA 2 California Department of Fish and Game (retired), Santa Cruz, CA, USA Impacts • Free-roaming cats are an important source of zoonotic diseases including rabies, Toxoplasma gondii, cutaneous larval migrans, tularemia and plague. • Free-roaming cats account for the most cases of human rabies exposure among domestic animals and account for approximately 1/3 of rabies post- exposure prophylaxis treatments in humans in the United States. • Trap–neuter–release (TNR) programmes may lead to increased naı¨ve populations of cats that can serve as a source of zoonotic diseases. Keywords: Summary Cutaneous larval migrans; free-roaming cats; rabies; toxoplasmosis; zoonoses Free-roaming cat populations have been identified as a significant public health threat and are a source for several zoonotic diseases including rabies, Correspondence: toxoplasmosis, cutaneous larval migrans because of various nematode parasites, R. Gerhold. Center for Wildlife Health, plague, tularemia and murine typhus. Several of these diseases are reported to Department of Forestry, Wildlife, and cause mortality in humans and can cause other important health issues includ- Fisheries, The University of Tennessee, ing abortion, blindness, pruritic skin rashes and other various symptoms. A Knoxville, TN 37996-4563, USA. Tel.: 865 974 0465; Fax: 865-974-0465; E-mail: recent case of rabies in a young girl from California that likely was transmitted [email protected] by a free-roaming cat underscores that free-roaming cats can be a source of zoonotic diseases. -
Flea Control in Cats Where Did My Cat Get Fleas? the Most Common Flea
Flea Control in Cats Where did my cat get fleas? The most common flea found on cats and dogs is the cat flea (Ctenocephalides felis), although any species of fleas, including fleas from rabbits, squirrels or other wildlife, can be found on cats. The most important source of cat fleas is newly emerged adult fleas from flea pupae in your house or yard. Adult fleas live, feed and mate on our pets; the female flea lays eggs that fall off into the environment where they hatch into larvae. The larvae eat organic debris until they mature into pupae. The pupae are encased in a sticky cocoon, helping them to camouflage in the environment and making them difficult to eradicate. Adult fleas will not emerge from the pupae until they sense an animal nearby to feed on. Newly hatched adult fleas jump onto a host animal to complete their life cycle. Two days after eating a blood meal from the host, the female flea begins to lay eggs. Under ideal conditions, the flea can complete its entire life cycle in as little as two weeks; in adverse conditions, the fleas within the pupae remain dormant, and can wait as much as a year to hatch, when conditions are more desirable. Homes with carpets and central heating provide ideal conditions for the year-round development of fleas. The highest numbers of flea eggs, larvae and pupae will be found in areas of the house where pets spend the most time, such as their beds and furniture. Even though fleas may be in your house, you probably won't see them. -
The Biology and Ecology of Cat Fleas and Advancements in Their Pest Management: a Review
insects Review The Biology and Ecology of Cat Fleas and Advancements in Their Pest Management: A Review Michael K. Rust ID Department of Entomology, University of California Riverside, Riverside, CA 92521, USA; [email protected]; Tel.: +1-951-827-5327 Academic Editors: Changlu Wang and Chow-Yang Lee Received: 7 August 2017; Accepted: 18 October 2017; Published: 27 October 2017 Abstract: The cat flea Ctenocephalides felis felis (Bouché) is the most important ectoparasite of domestic cats and dogs worldwide. It has been two decades since the last comprehensive review concerning the biology and ecology of C. f. felis and its management. Since then there have been major advances in our understanding of the diseases associated with C. f. felis and their implications for humans and their pets. Two rickettsial diseases, flea-borne spotted fever and murine typhus, have been identified in domestic animal populations and cat fleas. Cat fleas are the primary vector of Bartonella henselae (cat scratch fever) with the spread of the bacteria when flea feces are scratched in to bites or wounds. Flea allergic dermatitis (FAD) common in dogs and cats has been successfully treated and tapeworm infestations prevented with a number of new products being used to control fleas. There has been a continuous development of new products with novel chemistries that have focused on increased convenience and the control of fleas and other arthropod ectoparasites. The possibility of feral animals serving as potential reservoirs for flea infestations has taken on additional importance because of the lack of effective environmental controls in recent years. Physiological insecticide resistance in C. -
Domestic Dogs Are Mammalian Reservoirs for the Emerging
www.nature.com/scientificreports OPEN Domestic dogs are mammalian reservoirs for the emerging zoonosis fea-borne spotted fever, caused by Rickettsia felis Dinh Ng-Nguyen 1*, Sze-Fui Hii2, Minh-Trang Thi Hoang3, Van-Anh Thi Nguyen1, Robert Rees4,5, John Stenos2 & Rebecca Justine Traub4 Rickettsia felis is an obligate intracellular bacterium that is being increasingly recognized as an etiological agent of human rickettsial disease globally. The agent is transmitted through the bite of an infected vector, the cat fea, Ctenocephalides felis, however there is to date, no consensus on the pathogen’s vertebrate reservoir, required for the maintenance of this agent in nature. This study for the frst time, demonstrates the role of the domestic dog (Canis familiaris) as a vertebrate reservoir of R. felis. The ability of dogs to sustain prolonged periods of rickettsemia, ability to remain asymptomatically infected with normal haematological parameters and ability to act as biological vehicles for the horizontal transmission of R. felis between infected and uninfected feas provides indication of their status as a mammalian reservoir of this emerging zoonosis. Rickettsiae are obligate intracellular alpha-proteobacteria, maintained in nature through arthropod vectors and the vertebrate hosts they infect. Vertebrate hosts capable of developing rickettsemias, termed reservoir hosts, in turn, allow new lines of arthropod vectors to acquire infection. Except for epidemic typhus caused by Rickettsia prowazekii and transmitted by the human body louse, humans represent accidental or end-stage hosts for these agents and play no role in their life cycle. Rickettsia felis URRWXCal2 is being increasingly implicated as an important cause of non-specifc febrile illness in humans globally1–3. -
Holistic Understanding of Contemporary Ecosystems Requires Integration of Data on Domesticated, Captive and Cultivated Organisms
Biodiversity Data Journal 9: e65371 doi: 10.3897/BDJ.9.e65371 Forum Paper Holistic understanding of contemporary ecosystems requires integration of data on domesticated, captive and cultivated organisms Quentin Groom‡,§, Tim Adriaens |, Sandro Bertolino¶#, Kendra Phelps , Jorrit H Poelen¤, DeeAnn Marie Reeder«, David M Richardson§, Nancy B Simmons»,˄ Nathan Upham ‡ Meise Botanic Garden, Meise, Belgium § Centre for Invasion Biology, Department of Botany and Zoology, Stellenbosch University, Stellenbosch, South Africa | Research Inst. for Nature and Forest (INBO), Brussels, Belgium ¶ Department of Life Sciences and Systems Biology, University of Turin, Torino, Italy # EcoHealth Alliance, New York, United States of America ¤ Ronin Institute for Independent Scholarship, Montclair, United States of America « Bucknell University, Lewisburg, United States of America » Department of Mammalogy, Division of Vertebrate Zoology, American Museum of Natural History, New York, United States of America ˄ Arizona State University, Tempe, United States of America Corresponding author: Quentin Groom ([email protected]) Academic editor: Vincent Smith Received: 02 Mar 2021 | Accepted: 13 May 2021 | Published: 15 Jun 2021 Citation: Groom Q, Adriaens T, Bertolino S, Phelps K, Poelen JH, Reeder DM, Richardson DM, Simmons NB, Upham N (2021) Holistic understanding of contemporary ecosystems requires integration of data on domesticated, captive and cultivated organisms . Biodiversity Data Journal 9: e65371. https://doi.org/10.3897/BDJ.9.e65371 Abstract Domestic and captive animals and cultivated plants should be recognised as integral components in contemporary ecosystems. They interact with wild organisms through such mechanisms as hybridization, predation, herbivory, competition and disease transmission and, in many cases, define ecosystem properties. Nevertheless, it is widespread practice for data on domestic, captive and cultivated organisms to be excluded from biodiversity repositories, such as natural history collections. -
Molecular Investigations of Cat Fleas (Ctenocephalides Felis) Provide the First Evidence of Rickettsia Felis in Malta and Candidatus Rickettsia Senegalensis in Israel
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2018 Molecular investigations of cat fleas (Ctenocephalides felis) provide the first evidence of Rickettsia felis in Malta and Candidatus Rickettsia senegalensis in Israel Hornok, S ; Baneth, G ; Grima, A ; Takács, N ; Kontschán, J ; Meli, Marina L ; Suter, V ; Salant, H ; Farkas, R ; Hofmann-Lehmann, Regina Abstract: Rickettsia felis, the causative agent of flea-borne spotted fever, occurs on all continents except Antarctica, owing to the cosmopolitan distribution of its cat flea vector. In this study, cat fleas were collected in two countries where the occurrence of R. felis was either unknown (Malta) or where accurate prevalence data were lacking (Israel). Altogether 129 fleas were molecularly analysed for the presence of rickettsial DNA. On the basis of three genetic markers, R. felis was identified in 39.5% (15/38) of the cat fleas from Malta. Sequences showed 100% identity to each other and to relevant sequences inGenBank. Among the 91 cat fleas from Israel, two (2.2%) contained the DNA of Candidatus Rickettsia senegalen- sis. Phylogenetically, the R. felis and Candidatus R. senegalensis identified here clustered separately (with high support) but within one clade, which was a sister group to that formed by the typhus group and spotted fever group rickettsiae. This is the first record of R. felis in Malta and of Candidatus R. senegalensis outside its formerly reported geographical range including Africa, Asia and North America. DOI: https://doi.org/10.1016/j.nmni.2018.05.001 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-158200 Journal Article Published Version The following work is licensed under a Creative Commons: Attribution 4.0 International (CC BY 4.0) License. -
Development of Ctenocephalides Felis Felis (Siphonaptera: Pulicidae) in Different Substrates for Maintenance Under Laboratory Conditions
Short Communication ISSN 1984-2961 (Electronic) www.cbpv.org.br/rbpv Development of Ctenocephalides felis felis (Siphonaptera: Pulicidae) in different substrates for maintenance under laboratory conditions Desenvolvimento de Ctenocephalides felis felis (Siphonaptera: Pulicidae) em diferentes substratos para manutenção em condições laboratoriais Gabriela Pereira Salça de Almeida1; Diefrey Ribeiro Campos1; Barbara Rauta de Avelar1; Thalita Xavier de Araújo da Silva1; Monique Morais Lambert2; Mariana Silva Revoredo Alves2; Thaís Ribeiro Correia3* 1 Discente do Programa de Pós-graduação em Ciências Veterinárias, Universidade Federal Rural do Rio de Janeiro – UFRRJ, Seropédica, RJ, Brasil 2 Médico Veterinário Autônomo; Universidade Federal Rural do Rio de Janeiro – UFRRJ, Seropédica, RJ, Brasil 3 Departamento de Parasitologia Animal, Universidade Federal Rural do Rio de Janeiro – UFRRJ, Seropédica, RJ, Brasil How to cite: Almeida GPS, Campos DR, Avelar BR, Silva TXA, Lambert MM, Alves MSR, et al. Development of Ctenocephalides felis felis (Siphonaptera: Pulicidae) in different substrates for maintenance under laboratory conditions. Braz J Vet Parasitol 2020; 29(2): e022819. https://doi.org/10.1590/S1984-29612020047 Abstract The aim of this study was to evaluate the efficiency of different substrates for larval development of Ctenocephalides felis felis during its biological cycle. Eight hundred eggs of C. felis felis from a flea maintenance colony were used. Different diets were formulated, in which the main substrates were meat flour, powdered milk, sugar, lyophilized bovine blood, tick metabolites and lyophilized egg. The flea eggs were placed in test tubes (10 per tube) and approximately 2 g of the diet to be tested was added to each tube. There were 10 replicates for each substrate.