241 research outputs found
Persistent infection of pets within a household with three Bartonella species.
We monitored by blood culture and immunofluorescence assay (IFA) bartonella infection in one dog and eight cats in a household to determine the prevalence and persistence of the infection as well as its transmissibility to humans. Ectoparasite control was rigorously exercised. During a 3-year period, Bartonella clarridgeiae was recovered from one cat on two occasions, and B. henselae was isolated from another cat on four occasions. During a 16-month period, B. vinsonii subsp. berkhoffii was isolated from the dog on 8 of 10 culture attempts. Despite extensive household contact, the pet owner was seronegative to all three species by IFA for Bartonella-specific immunoglobulin G
Hemotropic mycoplasmas in little brown bats (Myotis lucifugus).
BackgroundHemotropic mycoplasmas are epicellular erythrocytic bacteria that can cause infectious anemia in some mammalian species. Worldwide, hemotropic mycoplasmas are emerging or re-emerging zoonotic pathogens potentially causing serious and significant health problems in wildlife. The objective of this study was to determine the molecular prevalence of hemotropic Mycoplasma species in little brown bats (Myotis lucifugus) with and without Pseudogymnoascus (Geomyces) destrucans, the causative agent of white nose syndrome (WNS) that causes significant mortality events in bats.MethodsIn order to establish the prevalence of hemotropic Mycoplasma species in a population of 68 little brown bats (Myotis lucifugus) with (n = 53) and without (n = 15) white-nose syndrome (WNS), PCR was performed targeting the 16S rRNA gene.ResultsThe overall prevalence of hemotropic Mycoplasmas in bats was 47%, with similar (p = 0.5725) prevalence between bats with WNS (49%) and without WNS (40%). 16S rDNA sequence analysis (~1,200 bp) supports the presence of a novel hemotropic Mycoplasma species with 91.75% sequence homology with Mycoplasma haemomuris. No differences were found in gene sequences generated from WNS and non-WNS animals.ConclusionsGene sequences generated from WNS and non-WNS animals suggest that little brown bats could serve as a natural reservoir for this potentially novel Mycoplasma species. Currently, there is minimal information about the prevalence, host-specificity, or the route of transmission of hemotropic Mycoplasma spp. among bats. Finally, the potential role of hemotropic Mycoplasma spp. as co-factors in the development of disease manifestations in bats, including WNS in Myotis lucifugus, remains to be elucidated
The Milky Way's Kiloparsec Scale Wind: A Hybrid Cosmic-Ray and Thermally Driven Outflow
We apply a wind model, driven by combined cosmic-ray and thermal-gas
pressure, to the Milky Way, and show that the observed Galactic diffuse soft
X-ray emission can be better explained by a wind than by previous static gas
models. We find that cosmic-ray pressure is essential to driving the observed
wind. Having thus defined a "best-fit" model for a Galactic wind, we explore
variations in the base parameters and show how the wind's properties vary with
changes in gas pressure, cosmic-ray pressure and density. We demonstrate the
importance of cosmic rays in launching winds, and the effect cosmic rays have
on wind dynamics. In addition, this model adds support to the hypothesis of
Breitschwerdt and collaborators that such a wind may help explain the
relatively small gradient observed in gamma-ray emission as a function of
galactocentric radius.Comment: 14 pages, 11 figures; Accepted to Ap
Metal Enrichment of the Intergalactic Medium in Cosmological Simulations
Observations have established that the diffuse intergalactic medium (IGM) at
z ~ 3 is enriched to ~0.1-1% solar metallicity and that the hot gas in large
clusters of galaxies (ICM) is enriched to 1/3-1/2 solar metallicity at z=0.
Metals in the IGM may have been removed from galaxies (in which they presumably
form) during dynamical encounters between galaxies, by ram-pressure stripping,
by supernova-driven winds, or as radiation-pressure driven dust efflux. This
study develops a method of investigating the chemical enrichment of the IGM and
of galaxies, using already completed cosmological simulations. To these
simulations, we add dust and (gaseous) metals, distributing the dust and metals
in the gas according to three simple parameterized prescriptions, one for each
enrichment mechanism. These prescriptions are formulated to capture the basic
ejection physics, and calibrated when possible with empirical data. Our results
indicate that dynamical removal of metals from >~ 3*10^8 solar mass galaxies
cannot account for the observed metallicity of low-column density Ly-alpha
absorbers, and that dynamical removal from >~ 3*10^10 solar mass galaxies
cannot account for the ICM metallicities. Dynamical removal also fails to
produce a strong enough mass-metallicity relation in galaxies. In contrast,
either wind or radiation-pressure ejection of metals from relatively large
galaxies can plausibly account for all three sets of observations (though it is
unclear whether metals can be distributed uniformly enough in the low-density
regions without overly disturbing the IGM, and whether clusters can be enriched
quite as much as observed). We investigate in detail how our results change
with variations in our assumed parameters, and how results for the different
ejection processes compare. (Abridged)Comment: Minor revision, 1 figure added addressing diffusion of metals after
their ejection. Accepted by ApJ. 31 EmulateApj Pages with 13 embedded
postscript figure
An XMM-Newton Observation of the Local Bubble Using a Shadowing Filament in the Southern Galactic Hemisphere
We present an analysis of the X-ray spectrum of the Local Bubble, obtained by
simultaneously analyzing spectra from two XMM-Newton pointings on and off an
absorbing filament in the Southern galactic hemisphere (b ~ -45 deg). We use
the difference in the Galactic column density in these two directions to deduce
the contributions of the unabsorbed foreground emission due to the Local
Bubble, and the absorbed emission from the Galactic halo and the extragalactic
background. We find the Local Bubble emission is consistent with emission from
a plasma in collisional ionization equilibrium with a temperature and an emission measure of 0.018 cm^{-6} pc. Our
measured temperature is in good agreement with values obtained from ROSAT
All-Sky Survey data, but is lower than that measured by other recent XMM-Newton
observations of the Local Bubble, which find
(although for some of these observations it is possible that the foreground
emission is contaminated by non-Local Bubble emission from Loop I). The higher
temperature observed towards other directions is inconsistent with our data,
when combined with a FUSE measurement of the Galactic halo O VI intensity. This
therefore suggests that the Local Bubble is thermally anisotropic.
Our data are unable to rule out a non-equilibrium model in which the plasma
is underionized. However, an overionized recombining plasma model, while
observationally acceptable for certain densities and temperatures, generally
gives an implausibly young age for the Local Bubble (\la 6 \times 10^5 yr).Comment: Accepted for publication in the Astrophysical Journal. 16 pages, 9
figure
Neurological Manifestations of Bartonellosis in Immunocompetent Patients: A Composite of Reports from 2005-2012
Abstract In recent years, an increasing number of Bartonella species have been identified as zoonotic pathogens, transmitted by animal bites, scratches or by arthropods. Although historically the term bartonellosis was attributed to infections with Bartonella bacilliformis, transmitted by sandflies in the Peruvian Andes, a more inclusive medical use of this term now includes infections caused by any Bartonella sp., anywhere in the world. Potentially, because Bartonella spp. can infect erythrocytes, endothelial cells, and various macrophage-type cells, including brain-derived dendritic cells in vitro, the clinical and pathological manifestations of bartonellosis appear to be very diverse. The purpose of this review is to focus attention on neurological bartonellosis cases reported in immunocompetent patients since 2005. Among these patients, disease course has varied substantially in length and severity, including one fatal case of encephalitis in a child. Based upon the evolving literature, a high clinical index of suspicion is warranted
PCR amplification of Bartonella koehlerae from human blood and enrichment blood cultures
<p>Abstract</p> <p>Background</p> <p>Cats appear to be the primary reservoir host for <it>Bartonella koehlerae</it>, an alpha Proteobacteria that is most likely transmitted among cat populations by fleas (<it>Ctenocephalides felis</it>). <it>Bartonella koehlerae </it>has caused endocarditis in a dog and in one human patient from Israel, but other clinically relevant reports involving this bacterium are lacking. Despite publication of numerous, worldwide epidemiological studies designed to determine the prevalence of <it>Bartonella </it>spp. bacteremia in cats, <it>B. koehlerae </it>has never been isolated using conventional blood agar plates. To date, successful isolation of <it>B. koehlerae </it>from cats and from the one human endocarditis patient has consistently required the use of chocolate agar plates.</p> <p>Results</p> <p>In this study, <it>Bartonella koehlerae </it>bacteremia was documented in eight immunocompetent patients by PCR amplification and DNA sequencing, either prior to or after enrichment blood culture using <it>Bartonella </it>alpha Proteobacteria growth medium. Presenting symptoms most often included fatigue, insomnia, joint pain, headache, memory loss, and muscle pain. Four patients were also infected with <it>Bartonella vinsonii </it>subsp. <it>berkhoffii </it>genotype II. After molecular documentation of <it>B. koehlerae </it>infection in these patients, a serological test was developed and serum samples were tested retrospectively. <it>Bartonella koehlerae </it>antibodies were not detected (titers < 1:16) in 30 healthy human control sera, whereas five of eight patient samples had <it>B. koehlerae </it>antibody titers of 1:64 or greater.</p> <p>Conclusions</p> <p>Although biased by a study population consisting of individuals with extensive arthropod and animal exposure, the results of this study suggest that <it>B. koehlerae </it>bacteremia is more common in immunocompetent people than has been previously suspected. Future studies should more thoroughly define modes of transmission and risk factors for acquiring infection with <it>B. koehlerae</it>. In addition, studies are needed to determine if <it>B. koehlerae </it>is a cause or cofactor in the development of arthritis, peripheral neuropathies or tachyarrhythmias in patients.</p
Ecological fitness and strategies of adaptation of Bartonella species to their hosts and vectors
Bartonella spp. are facultative intracellular bacteria that cause characteristic hostrestricted hemotropic infections in mammals and are typically transmitted by blood-sucking arthropods. In the mammalian reservoir, these bacteria initially infect a yet unrecognized primary niche, which seeds organisms into the blood stream leading to the establishment of a long-lasting intra-erythrocytic bacteremia as the hall-mark of infection. Bacterial type IV secretion systems, which are supra-molecular transporters ancestrally related to bacterial conjugation systems, represent crucial pathogenicity factors that have contributed to a radial expansion of the Bartonella lineage in nature by facilitating adaptation to unique mammalian hosts. On the molecular level, the type IV secretion system VirB/VirD4 is known to translocate a cocktail of different effector proteins into host cells, which subvert multiple cellular functions to the benefit of the infecting pathogen. Furthermore, bacterial adhesins mediate a critical, early step in the pathogenesis of the bartonellae by binding to extracellular matrix components of host cells, which leads to firm bacterial adhesion to the cell surface as a prerequisite for the efficient translocation of type IV secretion effector proteins. The best-studied adhesins in bartonellae are the orthologous trimeric autotransporter adhesins, BadA in Bartonella henselae and the Vomp family in Bartonella quintana. Genetic diversity and strain variability also appear to enhance the ability of bartonellae to invade not only specific reservoir hosts, but also accidental hosts, as shown for B. henselae. Bartonellae have been identified in many different blood-sucking arthropods, in which they are typically found to cause extracellular infections of the mid-gut epithelium. Adaptation to specific vectors and reservoirs seems to be a common strategy of bartonellae for transmission and host diversity. However, knowledge regarding arthropod specificity/res
Parallax of PSR J1744-1134 and the Local Interstellar Medium
We present the annual trigonometric parallax of PSR J1744-1134 derived from
an analysis of pulse times of arrival. The measured parallax, pi = 2.8+/-0.3
mas ranks among the most precisely determined distances to any pulsar. The
parallax distance of 357+/-39 pc is over twice that derived from the dispersion
measure using the Taylor & Cordes model for the Galactic electron distribution.
The mean electron density in the path to the pulsar, n_e = (0.0088 +/- 0.0009)
cm^{-3}, is the lowest for any disk pulsar. We have compared the n_e for PSR
J1744-1134 with those for another 11 nearby pulsars with independent distance
estimates. We conclude that there is a striking asymmetry in the distribution
of electrons in the local interstellar medium. The electron column densities
for pulsars in the third Galactic quadrant are found to be systematically
higher than for those in the first. The former correlate with the position of
the well known local HI cavity in quadrant three. The excess electrons within
the cavity may be in the form of HII clouds marking a region of interaction
between the local hot bubble and a nearby superbubble.Comment: revised version accepted for publication in ApJ Letters; reanalysis
of uncertainty in parallax measure and changes to fig
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