15 research outputs found

    Drivers of Bartonella infection in micromammals and their fleas in a Mediterranean peri-urban area

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    People living at the human/wildlife interface are at risk of becoming infected with Bartonella for which micromammals act as reservoir. We aimed to determine the factors related to the prevalence of Bartonella and its haplotype diversity in micromammals and in their fleas in a Mediterranean peri-urban environment. We analyzed 511 micromammals, chiefly 407 wood mice (Apodemus sylvaticus), captured into Barcelona metropolitan area (Spain) in spring and autumn from 2011 to 2013 in two natural and two adjacent residential areas, their fleas (grouped in 218 monospecific pools) and 29 fetuses from six Bartonella-positive female wood mice. Amplification of a fragment of ITS was carried out by real time PCR. Prevalence was 49% (57% in the dominant species, the wood mouse), and 12 haplotypes were detected. In general, prevalence was higher in those hosts more heavily infested by fleas, coincident with higher rates of capture, in autumn than in spring, and in adults than in juveniles. Prevalence did not differ between natural and residential areas except for one prevalent haplotype, which was more frequent in natural areas. Prevalence in flea pools (58%) was only explained by Bartonella occurrence in the pool host. In 56.4% of the flea pools with identified Bartonella haplotypes, we found the same haplotype in the host and in its flea pool. Prevalence in wood mouse fetuses was 69%, with at least one infected fetus in all litters, and two litters with all the fetuses infected. indicating that vertical transmission might be important in Bartonella epidemiology in the wood mouse. There is a hazard of Bartonella infection for people living in residential areas and those visiting peri-urban natural areas in Barcelona

    Infection and exposure to vector-borne pathogens in rural dogs and their ticks, Uganda

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    BACKGROUND: In rural parts of Africa, dogs live in close association with humans and livestock, roam freely, and usually do not receive prophylactic measures. Thus, they are a source of infectious disease for humans and for wildlife such as protected carnivores. In 2011, an epidemiological study was carried out around three conservation areas in Uganda to detect the presence and determine the prevalence of vector-borne pathogens in rural dogs and associated ticks to evaluate the risk that these pathogens pose to humans and wildlife. METHODS: Serum samples (n = 105), blood smears (n = 43) and blood preserved on FTA cards (n = 38) and ticks (58 monospecific pools of Haemaphysalis leachi and Rhipicephalus praetextatus including 312 ticks from 52 dogs) were collected from dogs. Dog sera were tested by indirect immunofluorescence to detect the presence of antibodies against Rickettsia conorii and Ehrlichia canis. Antibodies against R. conorii were also examined by indirect enzyme immunoassay. Real time PCR for the detection of Rickettsia spp., Anaplasmataceae, Bartonella spp. and Babesia spp. was performed in DNA extracted from FTA cards and ticks. RESULTS: 99 % of the dogs were seropositive to Rickettsia spp. and 29.5 % to Ehrlichia spp. Molecular analyses revealed that 7.8 % of the blood samples were infected with Babesia rossi, and all were negative for Rickettsia spp. and Ehrlichia spp. Ticks were infected with Rickettsia sp. (18.9 %), including R. conorii and R. massiliae; Ehrlichia sp. (18.9 %), including E. chaffeensis and Anaplasma platys; and B. rossi (1.7 %). Bartonella spp. was not detected in any of the blood or tick samples. CONCLUSIONS: This study confirms the presence of previously undetected vector-borne pathogens of humans and animals in East Africa. We recommend that dog owners in rural Uganda be advised to protect their animals against ectoparasites to prevent the transmission of pathogens to humans and wildlife

    Molecular detection of vector-borne pathogens in wild and domestic carnivores and their ticks at the human-wildlife interface

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    Urbanization of natural areas is considered one of the causes of the current apparent emergence of infectious diseases. Carnivores are among the species that adapt well to urban and periurban environments, facilitating cross-species disease transmission with domestic dogs and cats, and potentially with their owners. The prevalence of vector-borne pathogens (VBP) of zoonotic and veterinary interest was studied in sympatric wild and domestic carnivores into Barcelona Metropolitan Area (NE Spain). Blood or spleen samples from 130 animals, including 34 common genets (Genetta genetta), 12 red foxes (Vulpes vulpes), 10 stone martens (Martes foina), three Eurasian badgers (Meles meles), 34 free-roaming domestic cats and 37 dogs with outdoor access, were collected either in protected or adjacent residential areas. A total of 309 ticks (chiefly Rhipicephalus turanicus) were collected on these animals. The samples were analyzed with a battery of PCR assays targeting the DNA of Rickettsia spp., Anaplasmataceae, Coxiella burnetii, Bartonella spp., and Piroplasmida, and the amplicons were sequenced. The fox showed the highest prevalence (58%) and diversity of VBP (four pathogens), whereas none of the dogs were infected. Bartonella spp. (including B. clarridgeiae, B. henselae, and B. rochalimae) was the most prevalent pathogen. Infection of wild carnivores with Ehrlichia canis, C. burnetii, Theileria annae and Babesia vogeli was also confirmed, with some cases of coinfection observed. The presence of DNA of T. annae and B. vogeli was also confirmed in tick pools from four species of wild carnivores, supporting their role in piroplasmid life-cycle. By the sequencing of several target genes, DNA of Rickettsia massiliae was confirmed in 17 pools of Rh. turanicus, Rh. sanguineous, and Rh. pusillus from five different species, and Rickettsia conorii in one pool of Rh. sanguineous from a dog. None of the hosts from which these ticks were collected was infected by Rickettsia. Although carnivores may not be reservoir hosts for zoonotic Rickettsia, they can have an important role as mechanical dispersers of infected ticks

    Symbiotic microbes and potential pathogens in the intestine of dead southern right whale (Eubalaena australis) calves

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    Between 2003 and 2017, at least 706 southern right whale (Eubalaena australis) calves died at the Península Valdés calving ground in Argentina. Pathogenic microbes are often suggested to be the cause of stranding events in cetaceans; however, to date there is no evidence supporting bacterial infections as a leading cause of right whale calf deaths in Argentina. We used high-throughput sequencing and culture methods to characterize the bacterial communities and to detect potential pathogens from the intestine of stranded calves. We analyzed small and large intestinal contents from 44 dead calves that stranded at Península Valdés from 2005-2010 and found 108 bacterial genera, most identified as Firmicutes or Bacteroidetes, and 9 genera that have been previously implicated in diseases of marine mammals. Only one operational taxonomic unit was present in all samples and identified as Clostridium perfringens type A. PCR results showed that all C. perfringens isolates (n=38) were positive for alpha, 50% for beta 2 (n=19) and 47% for enterotoxin (CPE) genes (n=18). The latter is associated with food-poisoning and gastrointestinal diseases in humans and possibly other animals. The prevalence of the cpe gene found in the Valdés? calves is unusually high compared with other mammals. However, insufficient histologic evidence of gastrointestinal inflammation or necrosis (the latter possibly masked by autolysis) in the gut of stranded calves, and absence of enterotoxin detection precludes conclusions about the role of C. perfringens in calf deaths. Further work is required to determine whether C. perfringens or other pathogens detected in this study are causative agents of calf deaths at Península Valdés.Fil: Marón, Carina Flavia. Universidad Nacional de Córdoba. Facultad de Cs.exactas Físicas y Naturales. Departamento de Diversidad Biológica y Ecológica. Cátedra de Biología del Comportam. y Div. Animal Ii; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Kohl, Kevin D.. University of Pittsburgh; Estados UnidosFil: Chirife, Andrea. Programa de Monitoreo Sanitario Ballena Franca Austral; ArgentinaFil: Di Martino, Matías. Programa de Monitoreo Sanitario Ballena Franca Austral; ArgentinaFil: Fons, Mariola Penadés. Universidad Ceu Cardenal Herrera; EspañaFil: Navarro, Mauricio A.. University of California at Davis; Estados UnidosFil: Beingesser, Juliann. University of California at Davis; Estados UnidosFil: McAloose, Denise. Southern Right Whale Health Monitoring Program; ArgentinaFil: Uzal, Francisco A.. University of California at Davis; Estados UnidosFil: Dearing, M. Denise. University of Utah; Estados UnidosFil: Rowntree, Victoria J.. University of Utah; Estados Unidos. Instituto de Conservación de Ballenas; ArgentinaFil: Uhart, Marcela María. Southern Right Whale Health Monitoring Program; Argentina. University of Utah; Estados Unido

    Infection and exposure to vector-borne pathogens in rural dogs and their ticks, Uganda

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    In rural parts of Africa, dogs live in close association with humans and livestock, roam freely, and usually do not receive prophylactic measures. Thus, they are a source of infectious disease for humans and for wildlife such as protected carnivores. In 2011, an epidemiological study was carried out around three conservation areas in Uganda to detect the presence and determine the prevalence of vector-borne pathogens in rural dogs and associated ticks to evaluate the risk that these pathogens pose to humans and wildlife. Serum samples (n = 105), blood smears (n = 43) and blood preserved on FTA cards (n = 38) and ticks (58 monospecific pools of Haemaphysalis leachi and Rhipicephalus praetextatus including 312 ticks from 52 dogs) were collected from dogs. Dog sera were tested by indirect immunofluorescence to detect the presence of antibodies against Rickettsia conorii and Ehrlichia canis. Antibodies against R. conorii were also examined by indirect enzyme immunoassay. Real time PCR for the detection of Rickettsia spp., Anaplasmataceae, Bartonella spp. and Babesia spp. was performed in DNA extracted from FTA cards and ticks. 99 % of the dogs were seropositive to Rickettsia spp. and 29.5 % to Ehrlichia spp. Molecular analyses revealed that 7.8 % of the blood samples were infected with Babesia rossi, and all were negative for Rickettsia spp. and Ehrlichia spp. Ticks were infected with Rickettsia sp. (18.9 %), including R. conorii and R. massiliae ; Ehrlichia sp. (18.9 %), including E. chaffeensis and Anaplasma platys ; and B. rossi (1.7 %). Bartonella spp. was not detected in any of the blood or tick samples. This study confirms the presence of previously undetected vector-borne pathogens of humans and animals in East Africa. We recommend that dog owners in rural Uganda be advised to protect their animals against ectoparasites to prevent the transmission of pathogens to humans and wildlife

    Wildtype, grey-morph and partial grey-morph phenotypes of southern right whales.

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    <p><i>Wild-type</i> adults (panel a) have black skin and often have white skin patches on their bellies. <i>Grey morphs</i> (calf in panel b) are primarily white at birth with splatterings of rounded black spots that extend dorso-laterally around their bodies (calf in panel b). Their white skin becomes light grey or brown with age (panel c). <i>Partial grey morphs</i> are primarily black with splatterings of white skin at birth (calf in panel d) which also darkens with age (adults in panels b and d).. (Photos: J. Atkinson, Ocean Alliance).</p

    Light microscopy reveals reduced pigmentation and a decreased number of melanocytes in the affected skin of grey-morph SRWs.

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    <p>A comparison of Fontana Masson melanin staining is shown in wild type (Panels A, C, and E) versus grey-morph SRWs (Panels B, D, and F) at low-power (20X, Panels A and B), high-power (400X, Panels C and D), and extra high-power (600X, Panels E and F) magnification. Low-power magnification shows less melanin staining, particularly in the melanocytes distributed along the basal layer of the epidermal rete ridges (arrowheads, Panels A and B). Rete ridges and dermal papillae appear similar in grey-morph and wild-type whales. Dermal papillae are marked with “= >” in panels A, B and C. High-power magnification shows reduced melanin content and fewer positively-stained cells in the grey-morph skin (Panels C and D). Extra high-power magnification shows typical melanocyte dendrite morphology (arrowhead, Panels E and F) and normal melanosome transfer and capping of keratinocyte nuclei (asterisks, Panels E and F).</p

    Melanocyte counts are reduced in grey-morph relative to wild-type SRW skin.

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    <p>Bars represent the absolute number of melanocytes counted in grey-morph and wild-type whales. Darkly shaded bars represent the number of melanocytes in each of 5 high-powered fields and lightly shaded blue bars represent the number of melanocytes along each 0.25 mm of the basement membrane measured. Data were compared for both measurement methods using T-tests. Both tests yielded p-values smaller than 1x10<sup>-5</sup>.</p
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