The Role of Chiggers As Human Pathogens
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A Case Study of the Cuban Iguana (Cyclura Nubila)
Animal Conservation (1998) 1, 165–172 © 1998 The Zoological Society of London Printed in the United Kingdom The need for pre-release health screening in animal translocations: a case study of the Cuban iguana (Cyclura nubila) Allison C. Alberts1, Marcie L. Oliva2, Michael B. Worley1, Sam R. Telford, Jr3, Patrick J. Morris4 and Donald L. Janssen4 1 Center for Reproduction of Endangered Species, Zoological Society of San Diego, P.O. Box 551, San Diego, CA 92112, USA 2 Department of Pathology, Zoological Society of San Diego, P.O. Box 551, San Diego, CA 92112, USA 3 Florida Museum of Natural History, University of Florida, Gainesville, FL 32611, USA 4 Department of Veterinary Services, San Diego Zoo, P.O. Box 551, San Diego, CA 92112, USA (Received 21 October 1997; accepted 23 February 1998) Abstract A serious concern with the increasing use of translocation and reintroduction in animal conservation programs is the potential for disease transmission between captive and free-ranging populations. As part of an experimental headstarting program, 45 juvenile Cuban iguanas, Cyclura nubila, were artificially incubated, maintained in captivity for six to 18 months, and subsequently released into natural areas on the US Naval Base at Guantánamo Bay, Cuba. Prior to release, all animals under- went physical examinations, hematological analyses, plasma biochemical determinations, and blood and fecal parasite screening. Comparable data were collected from free-ranging juveniles to establish normal baseline values. Although all hematological parameters were within expected ranges for healthy reptiles, captive juveniles exhibited higher total leukocyte counts and percent lymphocytes, but lower percent heterophils, than free-ranging juveniles. -
SIP Newsletter 2015 June V4.Pages
Society for Invertebrate Pathology Newsletter Volume 48 Issue 2 June, 2015 Downtown Vancouver at Sunset. Photo Credit: Magnus3D Meeting Events: Saturday Tuesday Registration (2 pm - 8 pm) Concurrent Sessions Sunday Excursions and 5K Race BBQ at the Cheakamus Center SIP Council Meeting OECD Satellite Symposium Wednesday Bacteria Workshop Concurrent Sessions Opening Mixer Posters Monday Division Business Meetings Founders’ Lecture Thursday Plenary Symposium Concurrent Sessions Concurrent Sessions SIP Annual & Student Business Division Business Meetings Meetings Award Ceremonies and Banquet !1 From the President Dear SIP Colleagues, This communiqué is threefold. First, I would like to encourage those of you President who have yet to do so to register for the Peter Krell, Canada 2015 SIP in Vancouver Canada, second, convince those with a flair for Vice President writing to step up to replace Eric Haas Johannes Jehle, Germany Stapleton as SIP Newsletter Editor and Past President third, inform you about our Golden Jørgen Eilenberg, Denmark Jubilee Committee. The 48th SIP meeting is just around Secretary the corner, August 9 to 13, all in the Mary Barbercheck, USA newly opened “The Nest” at the beautiful University of British Treasurer Columbia campus, overlooking the Strait of Georgia between Stefan Jaronski, USA Vancouver and Vancouver Island, and only a short bicycle ride of about 90 miles (150 km) north of Seattle. There are many reasons Trustees to attend, just check out the meeting’s website on the SIP home Surendra Dara, USA Albrecht Koppenhofer, USA page. Famous for its natural beauty with great opportunities for Ed Lewis, USA hiking, canoeing and nature photography, along with both classical Monique van Oers, The Netherlands and aboriginal culture with a mixed east/west cuisine. -
Androgens and Ectoparasites As Proximate Factors
ANDROGENS AND ECTOPARASITES AS PROXIMATE FACTORS INFLUENCING GROWTH IN THE SEXUALLY DIMORPHIC LIZARD, SCELOPORUS UNDULATUS By NICHOLAS POLLOCK A dissertation submitted to the Graduate School-New Brunswick Rutgers, The State University of New Jersey In partial fulfillment of the requirements For the degree of Doctor of Philosophy Graduate Program in Ecology & Evolution Written under the direction of Dr. Henry B. John-Alder And approved by ____________________________________ ____________________________________ ____________________________________ New Brunswick, New Jersey October 2016 ABSTRACT OF THE DISSERTATION Androgens and ectoparasites as proximate factors influencing growth in the sexually dimorphic lizard, Sceloporus undulatus By NICHOLAS POLLOCK Dissertation Director: Dr. Henry B. John-Alder A growing body of evidence indicates that testosterone (T) plays an important role in regulating patterns of growth in lizards. Testosterone has also been found to facilitate the development of male-typical coloration and a suite of male behaviors that increase reproductive success. However, while T promotes male fitness through these characteristics, it appears to hinder fitness through direct molecular inhibition of growth and through indirect potential costs associated with increased parasitism. The relationship between T and ectoparasitism is complicated by seasonal variation in host circulating T levels and ectoparasite life cycles. It is unclear whether sex differences in ectoparasite loads are present year-round, are present only when circulating T is high in males, or are present only when ectoparasite abundances are high. Furthermore, it is often assumed that because ectoparasites feed by taking nutrients and energy from their hosts, then ectoparasites likely impact host growth. Effects of ectoparasitism on host growth may be particularly high in males if they have greater ectoparasite loads than females. -
Zoology Addition to the Mite Fauna in Human Habitation from South
Volume : 5 | Issue : 7 | July 2016 • ISSN No 2277 - 8179 | IF : 3.508 | IC Value : 69.48 Original Research Paper Original Research Paper Volume : 5 | Issue : 7 | July 2016 • ISSN No 2277 - 8179 | IF : 3.508 | IC Value : 69.48 Zoology Addition To The Mite Fauna in Human KEYWORDS : Human habitation, Prostigmata, Mesostigmata, Astigmata, Habitation From South Bengal South Bengal Post Graduate Department of Zoology, Vidyasagar College, Salt Lake City, CL Ananya Das Block, Kolkata 700 091 Post Graduate Department of Zoology, Vidyasagar College, Salt Lake City, CL S.K. Gupta Block, Kolkata 700 091 Post Graduate Department of Zoology, Vidyasagar College, Salt Lake City, CL N. Debnath Block, Kolkata 700 091 ABSTRACT The present paper reports the occurrence of 111 species of mites belonging to 69 genera,27 families under 3 orders collected from a total of 40 samples representing 5 different habitats viz. stored products, house dust, bird nests, cattle sheds and roof gardens from 5 districts of South Bengal. Among the 5 habitats, cattle shed provided richest diversity both in respect of species and genera followed by stored product habitat and the minimum was bird nest which represented only 11 species. The family level diversity was also highest in case of cattle sheds followed by stored products and the minimum was in roof garden. There was not a single species which could be collected from all the 5 habitats though; of course, there was 1 species which represented 4 out of 5 habitats. Therefore, cattle sheds proved to be habitat showing highest diversity. The order Prostigmata represented highest number of species followed by Astigmata. -
Sgienge Bulletin
THE UNIVERSITY OF KANSAS SGIENGE BULLETIN Vol. XXXVII, Px. II] June 29, 1956 [No. 19 of The Chigger Mites Kansas (Acarina, Trombiculidae ) BY Richard B. Loomis Abstract: Studies of the chigger mites in Kansas revealed 47 forms, con- sisting of 46 species in the following genera: Leeuwcnhoekia ( 1 ), Acomatacarus (3), Whartoraa (1), Hannemania (3), Trombicula (21), Speleocola (1), Euschbngastia (10), Pseudoschongastia (2), Cheladonta (1), Neoschongastia (2), and Walchia (1). Data were gathered in the period from 1947 to 1954. More than 14,000 mounted larvae were critically examined. All but one of the 47 forms were obtained from a total of 6,534 vertebrates of 194 species. Larvae of eight species of chiggers also were recovered from black plastic sampler plates placed on the substrate. Free-living nymphs and adults of all species seem to be active in warm weather. The time of oviposition differs in the different kinds, but there is little variation within a species. The exact time of emergence, abundance and disappearance of the larvae depends on the temperature of the environment. The species can be arranged according to their larval activity in two seasonal groups: the summer group (26 species) and the winter group (20 species). The seasonal overlap between these groups is slight. Rainfall and moisture content of the substrate affect the abundance of the larvae, but not the time of their emergence or disappearance. The summer species often have two genera- tions of larvae annually, but in the winter species no more than one generation is known. The larvae, normally parasitic on vertebrates, exhibit little host specificity. -
THE GENUS GUNTHERANA (Acarina, Trombiculidae)
Pacific Insects 2 (2) : 195-237 July 31, 1960 THE GENUS GUNTHERANA (Acarina, Trombiculidae) By Robert Domrow QUEENSLAND INSTITUTE OF MEDICAL RESEARCH, BRISBANE ABSTRACT The genus Guntherana is enlarged to include the chiggers from Australia and New Guinea previously assigned to Euschongastia s. 1. (except those of the subgenus Walchiel- la, which should be restored to generic rank). Two subgenera, Eerrickiella and Gun therana s. s., are recognized on both nymphal and larval characters, and each contains 2 species groups recognizable on larval characters alone. The subgeneric division by lar val characters parallels that by nymphal characters. Twenty-six species have been transferred, and 4 new species described, bringing the total to 33, including the 3 species already in the genus (kallipygos, tindalei, trans lucens'). Keys are given to the larval subgenera, species groups and species, but the nymphs are too alike morphologically to be profitably keyed, except at a subgeneric level. The following 26 larval names are combined for the first time with Guntherana: andromeda Womersley, antipodiana Hirst, cassiope Worn., coorongensis Hirst, dasycerci Hirst, derricki Worn., dumosa Worn., echymipera Worn. & Kohls, foliata Gunther, heaslipi Worn. & Heaslip, innisfailensis Worn. & Heas., mackerrasae Worn., mccullochi Worn., parva Worn., perameles Worn., peregrina Worn., Petrogale Worn., pseudomys Worn., queensland ica Worn., shieldsi Gun., similis Worn. & Heas., smithi Worn., trichosuri Worn., newmani Worn., womersleyi Gun., & wongabelensis Worn. Four new larval species are described from Queensland—G. (D.) petulans from Rattus assimilis, Melomys cervinipes and Hypsi prymnodon moschatus; G. (Z>.) rex from R. assimilis; G. (G.) emphyla from Isoodon macrourus, Perameles nasuta and M. cervinipes; and G. -
What's Eating You? Chiggers
CLOSE ENCOUNTERS WITH THE ENVIRONMENT What’s Eating You? Chiggers Dirk M. Elston, MD higger is the common name for the 6-legged larval form of a trombiculid mite. The larvae C suck blood and tissue fluid and may feed on a variety of animal hosts including birds, reptiles, and small mammals. The mite is fairly indiscrimi- nate; human hosts will suffice when the usual host is unavailable. Chiggers also may be referred to as harvest bugs, harvest lice, harvest mites, jiggers, and redbugs (Figure 1). The term jigger also is used for the burrowing chigoe flea, Tunga penetrans. Chiggers belong to the family Trombiculidae, order Acari, class Arachnida; many species exist. Trombiculid mites are oviparous; they deposit their eggs on leaves, blades of grass, or the open ground. After several days, the egg case opens, but the mite remains in a quiescent prelarval stage. Figure 1. Chigger mite. After this prelarval stage, the small 6-legged larvae become active and search for a host. During this larval 6-legged stage, the mite typically is found attaches at sites of constriction caused by clothing, attached to the host. After a prolonged meal, the where its forward progress has been impeded. Penile larvae drop off. Then they mature through the and scrotal lesions are not uncommon and may be 8-legged free-living nymph and adult stages. mistaken for scabies infestation. Seasonal penile Chiggers can be found throughout the world. In swelling, pruritus, and dysuria in children is referred the United States, they are particularly abundant in to as summer penile syndrome. -
Proceedings of the Indiana Academy of Science
Ectoparasites of Pine Voles, Microtus pinetorum, from Clark County, Illinois D. David Pascal, Jr. and John O. Whitaker, Jr. Department of Life Sciences Indiana State University Terre Haute, Indiana 47809 Introduction In studies on pine voles, only Hamilton (1938) and Benton (1955), both working in New York, attempted to collect and identify external parasites. Hamilton noted the mite, Laelaps kochi Oudemans, 1936 and lice of the genus Hoplopleura to be par- ticularly numerous. Benton reported Hoplopleura acanthopus (Burmeister, 1839) and Androlaelaps fahrenholzi (Berlese, 191 1) as the most abundant pine vole ectoparasites. Ferris (1921) reported H. acanthopus from pine voles in New York and Iowa. Another louse, Polyplax spinulosa (Burmeister, 1839), was found to infest pine voles in Georgia (Morlan, 1952), although Rattus norvegicus and R. rattus are the true hosts for this louse (Pratt and Karp, 1953; Wilson, 1961). The occurrence on pine voles was accidental. Mite records (other than chiggers) on Microtus pinetorum have been summarized by Whitaker and Wilson (1974), but include LAELAPIDAE: Androlaelaps fahrenholzi (Berlese, 1911), Laelaps kochi Oudemans, 1936, Haemogamasus longitarsus (Banks, 1910), H. liponyssoides Ewing, 1925, H. ambulans (Thorell, 1872), Laelaps alaskensis Grant, 1947, and Eulaelaps stabularis (Koch, 1836); GLYCYPHAGIDAE: Glycyphagus hypudaei (Koch, 1841) and Orycteroxenus soricis (Oudemans, 1915) LISTROPHORIDAE: Listrophorus pitymys Fain and Hyland, 1972; MYOBIIDAE Radfordia ensifera (Poppe, 1896) and R. lemnina (Koch, 1841); CHEYLETIDAE Eucheyletia bishoppi Baker, 1949. In addition, Smiley and Whitaker (1979) reported the following pygmephorid mites from Microtus pinetorum from Indiana: Pygmephorus equitrichosus Mahunka, 1975, P. hastatus Mahunka, 1973, P. scalopi Mahunka, 1973 and P. whitakeri Mahunka, 1973. -
Leptotrombidium Deliense
ISSN (Print) 0023-4001 ISSN (Online) 1738-0006 Korean J Parasitol Vol. 56, No. 4: 313-324, August 2018 ▣ MINI REVIEW https://doi.org/10.3347/kjp.2018.56.4.313 Research Progress on Leptotrombidium deliense 1,2 1,2 1 Yan Lv , Xian-Guo Guo *, Dao-Chao Jin 1Institute of Entomology, Guizhou University, and the Provincial Key Laboratory for Agricultural Pest Management in Mountainous Region, Guiyang 550025, P. R. China; 2Vector Laboratory, Institute of Pathogens and Vectors, Yunnan Provincial Key Laboratory for Zoonosis Control and Prevention, Dali University, Dali, Yunnan Province 671000, P. R. China Abstract: This article reviews Leptotrombidium deliense, including its discovery and nomenclature, morphological features and identification, life cycle, ecology, relationship with diseases, chromosomes and artificial cultivation. The first record of L. deliense was early in 1922 by Walch. Under the genus Leptotrombidium, there are many sibling species similar to L. de- liense, which makes it difficult to differentiate L. deliense from another sibling chigger mites, for example, L. rubellum. The life cycle of the mite (L. deliense) includes 7 stages: egg, deutovum (or prelarva), larva, nymphochrysalis, nymph, ima- gochrysalis and adult. The mite has a wide geographical distribution with low host specificity, and it often appears in differ- ent regions and habitats and on many species of hosts. As a vector species of chigger mite, L. deliense is of great impor- tance in transmitting scrub typhus (tsutsugamushi disease) in many parts of the world, especially in tropical regions of Southeast Asia. The seasonal fluctuation of the mite population varies in different geographical regions. The mite has been successfully cultured in the laboratory, facilitating research on its chromosomes, biochemistry and molecular biology. -
Gene Gain and Loss Events in Rickettsia and Orientia Species Kalliopi Georgiades1,2, Vicky Merhej1, Khalid El Karkouri1, Didier Raoult1, Pierre Pontarotti2*
Georgiades et al. Biology Direct 2011, 6:6 http://www.biology-direct.com/content/6/1/6 RESEARCH Open Access Gene gain and loss events in Rickettsia and Orientia species Kalliopi Georgiades1,2, Vicky Merhej1, Khalid El Karkouri1, Didier Raoult1, Pierre Pontarotti2* Abstract Background: Genome degradation is an ongoing process in all members of the Rickettsiales order, which makes these bacterial species an excellent model for studying reductive evolution through interspecies variation in genome size and gene content. In this study, we evaluated the degree to which gene loss shaped the content of some Rickettsiales genomes. We shed light on the role played by horizontal gene transfers in the genome evolution of Rickettsiales. Results: Our phylogenomic tree, based on whole-genome content, presented a topology distinct from that of the whole core gene concatenated phylogenetic tree, suggesting that the gene repertoires involved have different evolutionary histories. Indeed, we present evidence for 3 possible horizontal gene transfer events from various organisms to Orientia and 6 to Rickettsia spp., while we also identified 3 possible horizontal gene transfer events from Rickettsia and Orientia to other bacteria. We found 17 putative genes in Rickettsia spp. that are probably the result of de novo gene creation; 2 of these genes appear to be functional. On the basis of these results, we were able to reconstruct the gene repertoires of “proto-Rickettsiales” and “proto-Rickettsiaceae”, which correspond to the ancestors of Rickettsiales and Rickettsiaceae, respectively. Finally, we found that 2,135 genes were lost during the evolution of the Rickettsiaceae to an intracellular lifestyle. Conclusions: Our phylogenetic analysis allowed us to track the gene gain and loss events occurring in bacterial genomes during their evolution from a free-living to an intracellular lifestyle. -
Scrub Typhus and Molecular Characterization of Orientia Tsutsugamushi from Central Nepal
pathogens Article Scrub Typhus and Molecular Characterization of Orientia tsutsugamushi from Central Nepal Rajendra Gautam 1, Keshab Parajuli 1, Mythili Tadepalli 2, Stephen Graves 2, John Stenos 2,* and Jeevan Bahadur Sherchand 1 1 Department of Microbiology, Maharajgunj Medical Campus, Institute of Medicine, Kathmandu 44600, Nepal; [email protected] (R.G.); [email protected] (K.P.); [email protected] (J.B.S.) 2 Australian Rickettsial Reference Laboratory, Geelong, VIC 3220, Australia; [email protected] (M.T.); [email protected] (S.G.) * Correspondence: [email protected]; Tel.: +61-342151357 Abstract: Scrub typhus is a vector-borne, acute febrile illness caused by Orientia tsutsugamushi. Scrub typhus continues to be an important but neglected tropical disease in Nepal. Information on this pathogen in Nepal is limited to serological surveys with little information available on molecular methods to detect O. tsutsugamushi. Limited information exists on the genetic diversity of this pathogen. A total of 282 blood samples were obtained from patients with suspected scrub typhus from central Nepal and 84 (30%) were positive for O. tsutsugamushi by 16S rRNA qPCR. Positive samples were further subjected to 56 kDa and 47 kDa molecular typing and molecularly compared to other O. tsutsugamushi strains. Phylogenetic analysis revealed that Nepalese O. tsutsugamushi strains largely cluster together and cluster away from other O. tsutsugamushi strains from Asia and elsewhere. One exception was the sample of Nepal_1, with its partial 56 kDa sequence clustering Citation: Gautam, R.; Parajuli, K.; more closely with non-Nepalese O. tsutsugamushi 56 kDa sequences, potentially indicating that Tadepalli, M.; Graves, S.; Stenos, J.; homologous recombination may influence the genetic diversity of strains in this region. -
ESCCAP Guidelines Final
ESCCAP Malvern Hills Science Park, Geraldine Road, Malvern, Worcestershire, WR14 3SZ First Published by ESCCAP 2012 © ESCCAP 2012 All rights reserved This publication is made available subject to the condition that any redistribution or reproduction of part or all of the contents in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise is with the prior written permission of ESCCAP. This publication may only be distributed in the covers in which it is first published unless with the prior written permission of ESCCAP. A catalogue record for this publication is available from the British Library. ISBN: 978-1-907259-40-1 ESCCAP Guideline 3 Control of Ectoparasites in Dogs and Cats Published: December 2015 TABLE OF CONTENTS INTRODUCTION...............................................................................................................................................4 SCOPE..............................................................................................................................................................5 PRESENT SITUATION AND EMERGING THREATS ......................................................................................5 BIOLOGY, DIAGNOSIS AND CONTROL OF ECTOPARASITES ...................................................................6 1. Fleas.............................................................................................................................................................6 2. Ticks ...........................................................................................................................................................10