Literature DB >> 19751613

Fatal borreliosis in bat caused by relapsing fever spirochete, United Kingdom.

Nicholas J Evans, Kevin Bown, Dorina Timofte, Vic R Simpson, Richard J Birtles.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19751613      PMCID: PMC2815988          DOI: 10.3201/eid1508.090475

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


× No keyword cloud information.
To the Editor: Tick-borne relapsing fevers caused by members of the genus Borrelia have been encountered throughout Africa, Asia, the Americas and, rarely, in southern Europe (). The Borrelia species associated with relapsing fevers form a monophyletic group within the genus, although not all members of this group have yet been implicated as agents of human disease. For example, a novel spirochete that is closely related to the relapsing fever agent Borrelia turicatae has recently been detected in Carios kelleyi, an argasid bat tick (,). We report the discovery of a spirochete causing fatal borreliosis in a bat in the United Kingdom. The infected bat was a juvenile female Pipistrellus species that was found alive but on the ground near the town of Mevagissy in southwestern England in August 2008; despite rehabilitation efforts, it died a few days later. A postmortem examination showed pale skeletal muscles, anemia, excess blood-tinged pleural fluid, a healthy thymus, but enlarged cranial thoracic lymph nodes. The liver was greatly enlarged and mottled, the spleen was also large and unusually dark, and the adrenal glands were enlarged and pale with areas of hemorrhage. The kidneys were pale with a fine speckling pattern over the cortex. Histopathologic examination of the liver showed multifocal necrosis and vacuolation of hepatocytes and infiltration by macrophages. The lungs were congested and infiltrated by inflammatory cells, and large numbers of granulocytes were found in the blood vessels. The spleen showed marked extramedullary hemopoiesis. Tissue sections stained by the Warthin-Starry technique exhibited numerous long, undulating, argophilic bacilli. These organisms were present in large numbers in the liver lesions (Figure), but were also found in the parenchyma of lung and spleen and in blood vessels.
Figure

A) Warthin-Starry–stained section of bat liver showing numerous spirochetes. B) Phylogram inferred from 776-bp alignment of flaB fragments obtained from infected bat liver tissue and for other members of the relapsing fever group of Borrelia species for which sequence data were available. B. burgdorferi is included as an outgroup. The numbers appearing after the names of the Borrelia species are the relevant GenBank accession numbers. Scale bar indicates nucleotides substitutions per site.

A) Warthin-Starry–stained section of bat liver showing numerous spirochetes. B) Phylogram inferred from 776-bp alignment of flaB fragments obtained from infected bat liver tissue and for other members of the relapsing fever group of Borrelia species for which sequence data were available. B. burgdorferi is included as an outgroup. The numbers appearing after the names of the Borrelia species are the relevant GenBank accession numbers. Scale bar indicates nucleotides substitutions per site. On the basis of these observations, a diagnosis of fatal hepatitis and septicemia caused by a spirochete was made. DNA from the bat’s liver was extracted and analyzed by using a PCR specific for an almost complete fragment of the 16S rRNA-encoding gene, as previously described (), but with an annealing temperature of 45°C. This DNA extract was also incorporated into PCR assays targeting glpQ and flaB gene fragments (). The products of these reactions were sequenced, and sequence data were assembled and analyzed by using Staden () and MEGA (). We obtained unambiguous sequence data for all 3 loci, comprising of 1,364 bp of the 16S rRNA-encoding gene (GenBank accession no. FJ868583), 1,239 bp of flaB and flanking regions (GenBank accession no. FJ868584), and 480 bp of glpQ (GenBank accession no. FJ868585). Each of these was aligned with homologous sequences available for other Borrelia species and used for phylogenetic analyses. Inferences made by using all loci were congruent, with the UK bat–associated spirochete lying close to, but distinct from, a cluster containing B. recurrentis, B. duttonii, and B. crocidurae (Figure; data not shown). These 3 species are associated with relapsing fevers in Africa and Asia. The UK bat–associated spirochete bore no specific evolutionary relatedness to B. johnsonii, the newly characterized member of the relapsing fever group of Borrelia species associated with C. kellyi in the United States (Figure) (). An Argas vespertilionis larval tick was found attached to the infected bat and may have been the source of its infection. PCR was not performed on the tick because it was near-replete with blood that was intensely infected with spirochetes. A. vespertilionis, commonly known as the short-legged bat tick, is widely distributed, parasitizing numerous bat species across Europe, southern Asia, and North Africa (). Given the close relationship between the novel spirochete we encountered and known pathogens, the reported propensity of A. vespertilionis to bite humans (), and the wide geographic range of this tick, our findings have repercussions for public health in many parts of the Old World. Furthermore, although bats are likely the reservoir host for this organism, our study also identifies it as a pathogen, and as such its discovery has implications for the conservation of numerous threatened bat species across Europe and throughout the world.
  8 in total

Review 1.  Epidemiology of relapsing fever borreliosis in Europe.

Authors:  Stanislas Rebaudet; Philippe Parola
Journal:  FEMS Immunol Med Microbiol       Date:  2006-10

2.  MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0.

Authors:  Koichiro Tamura; Joel Dudley; Masatoshi Nei; Sudhir Kumar
Journal:  Mol Biol Evol       Date:  2007-05-07       Impact factor: 16.240

Review 3.  The Staden sequence analysis package.

Authors:  R Staden
Journal:  Mol Biotechnol       Date:  1996-06       Impact factor: 2.695

4.  Phylogenetic analysis of the spirochetes Borrelia parkeri and Borrelia turicatae and the potential for tick-borne relapsing fever in Florida.

Authors:  Tom G Schwan; Sandra J Raffel; Merry E Schrumpf; Paul F Policastro; Julie A Rawlings; Robert S Lane; Edward B Breitschwerdt; Stephen F Porcella
Journal:  J Clin Microbiol       Date:  2005-08       Impact factor: 5.948

5.  Geographical distribution, host associations, and vector roles of ticks (Acari: Ixodidae, Argasidae) in Sweden.

Authors:  T G Jaenson; L Tälleklint; L Lundqvist; B Olsen; J Chirico; H Mejlon
Journal:  J Med Entomol       Date:  1994-03       Impact factor: 2.278

6.  Association of unique, isolated treponemes with bovine digital dermatitis lesions.

Authors:  Nicholas J Evans; Jennifer M Brown; Ibrahim Demirkan; Prem Singh; Brian Getty; Dorina Timofte; W Daan Vink; Richard D Murray; Roger W Blowey; Richard J Birtles; C Anthony Hart; Stuart D Carter
Journal:  J Clin Microbiol       Date:  2009-01-14       Impact factor: 5.948

7.  Characterization of a novel relapsing fever spirochete in the midgut, coxal fluid, and salivary glands of the bat tick Carios kelleyi.

Authors:  Tom G Schwan; Sandra J Raffel; Merry E Schrumpf; James S Gill; Joseph Piesman
Journal:  Vector Borne Zoonotic Dis       Date:  2009-12       Impact factor: 2.133

8.  Novel relapsing fever spirochete in bat tick.

Authors:  James S Gill; Amy J Ullmann; Amanda D Loftis; Tom G Schwan; Sandra J Raffel; Merry E Schrumpf; Joseph Piesman
Journal:  Emerg Infect Dis       Date:  2008-03       Impact factor: 6.883

  8 in total
  23 in total

1.  Ticks (Acari: Argasidae, Ixodidae) parasitizing bats in the central Balkans.

Authors:  J Burazerović; S Ćakić; D Mihaljica; R Sukara; D Ćirović; S Tomanović
Journal:  Exp Appl Acarol       Date:  2015-02-26       Impact factor: 2.132

2.  Bartonella species in bats (Chiroptera) and bat flies (Nycteribiidae) from Nigeria, West Africa.

Authors:  Joshua Kamani; Gad Baneth; Mark Mitchell; Kosta Y Mumcuoglu; Ricardo Gutiérrez; Shimon Harrus
Journal:  Vector Borne Zoonotic Dis       Date:  2014-09       Impact factor: 2.133

3.  Eco-epidemiology of Novel Bartonella Genotypes from Parasitic Flies of Insectivorous Bats.

Authors:  Attila D Sándor; Mihály Földvári; Aleksandra I Krawczyk; Hein Sprong; Alexandra Corduneanu; Levente Barti; Tamás Görföl; Péter Estók; Dávid Kováts; Sándor Szekeres; Zoltán László; Sándor Hornok; Gábor Földvári
Journal:  Microb Ecol       Date:  2018-04-29       Impact factor: 4.552

4.  Novel relapsing fever Borrelia detected in African penguins (Spheniscus demersus) admitted to two rehabilitation centers in South Africa.

Authors:  Michael J Yabsley; Nola J Parsons; Elizabeth C Horne; Barbara C Shock; Michaelle Purdee
Journal:  Parasitol Res       Date:  2011-08-26       Impact factor: 2.289

5.  The critical role of permanent voucher specimens of hosts and vectors in public health and epidemiology.

Authors:  A Townsend Peterson
Journal:  Emerg Infect Dis       Date:  2010-02       Impact factor: 6.883

6.  First Record of a Suspected Human-Pathogenic Borrelia Species in Populations of the Bat Tick Carios vespertilionis in Sweden.

Authors:  Thomas G T Jaenson; Peter Wilhelmsson
Journal:  Microorganisms       Date:  2021-05-20

7.  Borrelia, Rickettsia, and Ehrlichia species in bat ticks, France, 2010.

Authors:  Cristina Socolovschi; Tahar Kernif; Didier Raoult; Philippe Parola
Journal:  Emerg Infect Dis       Date:  2012-12       Impact factor: 6.883

8.  Spatial disaggregation of tick occurrence and ecology at a local scale as a preliminary step for spatial surveillance of tick-borne diseases: general framework and health implications in Belgium.

Authors:  Valerie Obsomer; Marc Wirtgen; Annick Linden; Edwin Claerebout; Paul Heyman; Dieter Heylen; Maxime Madder; Jo Maris; Maude Lebrun; Wesley Tack; Laetitia Lempereur; Thierry Hance; Georges Van Impe
Journal:  Parasit Vectors       Date:  2013-06-22       Impact factor: 3.876

9.  Diseases in free-ranging bats from Germany.

Authors:  Kristin Mühldorfer; Stephanie Speck; Gudrun Wibbelt
Journal:  BMC Vet Res       Date:  2011-10-18       Impact factor: 2.741

10.  Ecological and evolutionary drivers of haemoplasma infection and bacterial genotype sharing in a Neotropical bat community.

Authors:  Daniel J Becker; Kelly A Speer; Alexis M Brown; M Brock Fenton; Alex D Washburne; Sonia Altizer; Daniel G Streicker; Raina K Plowright; Vladimir E Chizhikov; Nancy B Simmons; Dmitriy V Volokhov
Journal:  Mol Ecol       Date:  2020-04-21       Impact factor: 6.185

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.