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Avian malaria co-infections confound infectivity and vector competence assays of Plasmodium homopolare.
Currently, there are very few studies of avian malaria that investigate relationships among the host-vector-parasite triad concomitantly. In the current study, we experimentally measured the vector competence of several Culex mosquitoes for a newly described avian malaria parasite, Plasmodium homopolare. Song sparrow (Melospiza melodia) blood infected with a low P. homopolare parasitemia was inoculated into a naïve domestic canary (Serinus canaria forma domestica). Within 5 to 10 days post infection (dpi), the canary unexpectedly developed a simultaneous high parasitemic infection of Plasmodium cathemerium (Pcat6) and a low parasitemic infection of P. homopolare, both of which were detected in blood smears. During this infection period, PCR detected Pcat6, but not P. homopolare in the canary. Between 10 and 60 dpi, Pcat6 blood stages were no longer visible and PCR no longer amplified Pcat6 parasite DNA from canary blood. However, P. homopolare blood stages remained visible, albeit still at very low parasitemias, and PCR was able to amplify P. homopolare DNA. This pattern of mixed Pcat6 and P. homopolare infection was repeated in three secondary infected canaries that were injected with blood from the first infected canary. Mosquitoes that blood-fed on the secondary infected canaries developed infections with Pcat6 as well as another P. cathemerium lineage (Pcat8); none developed PCR detectable P. homopolare infections. These observations suggest that the original P. homopolare-infected songbird also had two un-detectable P. cathemerium lineages/strains. The vector and host infectivity trials in this study demonstrated that current molecular assays may significantly underreport the extent of mixed avian malaria infections in vectors and hosts
Identifying avian malaria vectors: sampling methods influence outcomes
Background The role of vectors in the transmission of avian malaria parasites is currently understudied. Many studies that investigate parasite-vector relationships use limited trapping techniques and/or identify potential competent vectors in the field in such ways that cannot distinguish between an infected or infectious vector. Without the use of multiple trapping techniques that address the specific biology of diverse mosquito species, and without looking at the infection status of individual mosquitoes, it is not possible to make dependable conclusions on the role of mosquitoes in the transmission of avian malaria parasites. Methods We conducted two years of mosquito collections at a riparian preserve in California where a wide diversity of species were collected with multiple trap types. We hypothesized that competent mosquito species can influence the distribution and diversity of avian malaria parasites by acting as a compatibility filter for specific Plasmodium species. To determine the infection status of all individual mosquitoes for Plasmodium species/lineages, amplification within the cytochrome b gene was carried out on over 3000 individual mosquito thoraxes, and for those that tested positive we then repeated the same process for abdomens and salivary glands. Results Our data show heterogeneity in the transmissibility of Plasmodium among ornithophillic mosquito species. More specifically, Culex stigmatosoma appears to not be a vector of Plasmodium homopolare, a parasite that is prevalent in the avian population, but is a vector of multiple other Plasmodium species/lineages. Conclusions Our results suggest that conclusions made on the role of vectors from studies that do not use different mosquito trapping methods should be re-evaluated with caution, as we documented the potential for trapping biases, which may cause studies to miss important roles of specific mosquito species in the transmission of avian malaria. Moreover, we document heterogeneity in the transmission of Plasmodium spp. by mosquitoes can influence Plasmodium diversity and prevalence in specific locations to Plasmodium-vector incompatibilities
Precession of the Super-Massive Black Hole in NGC 1275 (3C 84)?
The X-ray holes at the centre of the Perseus Cluster of galaxies are not all
at the same position angle with respect to the centre of the cluster. This
configuration would result if the jet inflating the bubbles is precessing, or
moving around, and the bubbles detach at different times. The orientations
which best fit the observed travel directions are an inclination of the
precession axis to the line of sight of 120 degrees and an opening angle of 50
degrees. From the timescales for the bubbles seen in the cluster, the
precession timescale, t_prec, is around 3.3x10^7 yrs. The bubbles rising up
through different parts of the cluster may have interacted with the central
cool gas, forming the whorl of cool gas observed in the temperature structure
of the cluster. The dynamics of bubbles rising in fluids is discussed. The
conditions present in the cluster are such that oscillatory motion, observed
for bubbles rising in fluids on Earth, should take place. However the timescale
for this motion is longer than that taken for the bubbles to evolve into
spherical cap bubbles, which do not undergo a path instability, so such motion
is not expected to occur.Comment: 9 pages, accepted for publication in MNRA
C-reactive protein, interleukin-6, and prostate cancer risk in men aged 65 years and older.
Inflammation is believed to play a role in prostate cancer (PCa) etiology, but it is unclear whether inflammatory markers C-reactive protein (CRP) and interleukin-6 (IL-6) associate with PCa risk in older men. Using Cox regression, we assessed the relationship between baseline concentrations of CRP and IL-6 and the subsequent PCa risk in the Cardiovascular Health Study, a population-based cohort study of mostly European American men of ages >64 years (n = 2,234; mean follow-up = 8.7 years; 215 incident PCa cases). We also tested associations between CRP and IL-6 tagSNPs and PCa risk, focusing on SNPs that are known to associate with circulating CRP and/or IL-6. Neither CRP nor IL-6 blood concentrations was associated with PCa risk. The C allele of IL-6 SNP rs1800795 (-174), a known functional variant, was associated with increased risk in a dominant model (HR = 1.44; 95% CI = 1.03-2.01; p = 0.03), but was not statistically significant after accounting for multiple tests (permutation p = 0.21). Our results suggest that circulating CRP and IL-6 do not influence PCa risk. SNPs at the CRP locus are not associated with PCa risk in this cohort, while the association between rs1800795 and PCa risk warrants further investigation
Common Coding Variants of the HNF1A Gene Are Associated With Multiple Cardiovascular Risk Phenotypes in Community-Based Samples of Younger and Older European-American Adults: The Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study
The transcription factor hepatocyte nuclear factor 1 (HNF-1) α regulates the activity of a number of genes involved in innate immunity, blood coagulation, lipid and glucose transport and metabolism, and cellular detoxification. Common polymorphisms of the HNF-1α gene (HNF1A) were recently associated with plasma C-reactive protein (CRP) and gamma-glutamyl transferase (GGT) concentration in middle-aged to older European-Americans (EA)
Polymorphisms of the IL1-Receptor Antagonist Gene (IL1RN) Are Associated With Multiple Markers of Systemic Inflammation
Circulating levels of acute phase reactant proteins such as plasma C-reactive protein (CRP) are likely influenced by multiple genes regulating the innate immune response
Avian Influenza in Wild Birds: Environmental Sampling for the Rapid Detection of Avian Influenza Viruses
All subtypes of influenza Type A viruses infect wild birds, especially waterfowl and shorebirds, but rarely cause disease or mortality in these aquatic species. Aquatic birds are the natural reservoirs for low pathogenic avian influenza viruses (LPAI) that are distributed globally. However, some AI subtypes can be virulent in other animals and humans and some highly pathogenic AI viruses (HPAI) have caused major outbreaks in poultry and even pandemics in the human population. The emergence of a HPAl H5N1 subtype in southeast Asian poultry in 1997 subsequently involved migratory waterfowl in 2005 and has since spread westward throughout the Asian, European, and African continents. This rapid continental spread planned animal and human health agencies in North America and initiated the establishment of a National Strategy for Pandemic influenza in the United States to increase and expand surveillance for the early detection of this virus, to improve and expand preventative measures, and to develop contingency responses to possible outbreaks. One of the methods of emergency surveillance developed and implemented was an interagency, early detection system for HPAI H5N1 avian influenza in wild migratory birds with the potential to bring in the virus from Asia or Europe and spread it throughout North America.
As part of this early detection system, the Wildlife Services National Wildlife Research Center developed testing methods, sampling protocols, guidelines, and analyzed 50,184 avian fecal samples collected by Wildlife Service biologists in 50 states and the U. S. territories. Samples were pooled in the laboratory (n = 10,541 pools) and analyzed using RT-PCR. AI viruses were detected in 4.0% of the 10,541 sample pools analyzed and H5/H7 subtypes were detected in 0.2% of the sample pools. Positive H5 and H7 subtypes were shipped to the National Veterinary Services Laboratory for further evaluation and confirmation. This monitoring effort was successful in detecting AI viruses in environmental samples and has proven to be a rapid and cost effective surveillance method
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk
BACKGROUND: Menopausal hormone therapy (MHT) use has been consistently associated with a decreased risk of colorectal cancer (CRC) in women. Our aim was to use a genome-wide gene-environment interaction analysis to identify genetic modifiers of CRC risk associated with use of MHT.
METHODS: We included 10 835 postmenopausal women (5419 cases and 5416 controls) from 10 studies. We evaluated use of any MHT, oestrogen-only (E-only) and combined oestrogen-progestogen (E+P) hormone preparations. To test for multiplicative interactions, we applied the empirical Bayes (EB) test as well as the Wald test in conventional case-control logistic regression as primary tests. The Cocktail test was used as secondary test.
RESULTS: The EB test identified a significant interaction between rs964293 at 20q13.2/CYP24A1 and E+P (interaction OR (95% CIs)=0.61 (0.52-0.72), P=4.8 × 10(-9)). The secondary analysis also identified this interaction (Cocktail test OR=0.64 (0.52-0.78), P=1.2 × 10(-5) (alpha threshold=3.1 × 10(-4)). The ORs for association between E+P and CRC risk by rs964293 genotype were as follows: C/C, 0.96 (0.61-1.50); A/C, 0.61 (0.39-0.95) and A/A, 0.40 (0.22-0.73), respectively.
CONCLUSIONS: Our results indicate that rs964293 modifies the association between E+P and CRC risk. The variant is located near CYP24A1, which encodes an enzyme involved in vitamin D metabolism. This novel finding offers additional insight into downstream pathways of CRC etiopathogenesis
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