Francisella tularensis Transmission by Solid Organ Transplantation, 20171.

In July 2017, fever and sepsis developed in 3 recipients of solid organs (1 heart and 2 kidneys) from a common donor in the United States; 1 of the kidney recipients died. Tularemia was suspected only after blood cultures from the surviving kidney recipient grew Francisella species. The organ donor, a middle-aged man from the southwestern United States, had been hospitalized for acute alcohol withdrawal syndrome, pneumonia, and multiorgan failure. F. tularensis subsp. tularensis (clade A2) was cultured from archived spleen tissue from the donor and blood from both kidney recipients. Whole-genome multilocus sequence typing indicated that the isolated strains were indistinguishable. The heart recipient remained seronegative with negative blood cultures but had been receiving antimicrobial drugs for a medical device infection before transplant. Two lagomorph carcasses collected near the donor's residence were positive by PCR for F. tularensis subsp. tularensis (clade A2). This investigation documents F. tularensis transmission by solid organ transplantation

Buffy coat specimens remain viable as a DNA source for highly multiplexed genome-wide genetic tests after long term storage

<p>Abstract</p> <p>Background</p> <p>Blood specimen collection at an early study visit is often included in observational studies or clinical trials for analysis of secondary outcome biomarkers. A common protocol is to store buffy coat specimens for future DNA isolation and these may remain in frozen storage for many years. It is uncertain if the DNA remains suitable for modern genome wide association (GWA) genotyping.</p> <p>Methods</p> <p>We isolated DNA from 120 Action to Control Cardiovascular Risk in Diabetes (ACCORD) clinical trial buffy coats sampling a range of storage times up to 9 years and other factors that could influence DNA yield. We performed TaqMan SNP and GWA genotyping to test whether the DNA retained integrity for high quality genetic analysis.</p> <p>Results</p> <p>We tested two QIAGEN automated protocols for DNA isolation, preferring the Compromised Blood Protocol despite similar yields. We isolated DNA from all 120 specimens (yield range 1.1-312 ug per 8.5 ml ACD tube of whole blood) with only 3/120 samples yielding < 10 ug DNA. Age of participant at blood draw was negatively associated with yield (mean change -2.1 ug/year). DNA quality was very good based on gel electrophoresis QC, TaqMan genotyping of 6 SNPs (genotyping no-call rate 1.1% in 702 genotypes), and excellent quality GWA genotyping data (maximum per sample genotype missing rate 0.64%).</p> <p>Conclusions</p> <p>When collected as a long term clinical trial or biobank specimen for DNA, buffy coats can be stored for up to 9 years in a -80degC frozen state and still produce high yields of DNA suitable for GWA analysis and other genetic testing.</p> <p>Trial Registration</p> <p>The Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial is registered with ClinicalTrials.gov, number <a href="http://www.clinicaltrials.gov/ct2/show/NCT00000620">NCT00000620</a>.</p

Genetic identification of unique immunological responses in mice infected with virulent and attenuated Francisella tularensis

Francisella tularensis is a category A select agent based on its infectivity and virulence but disease mechanisms in infection remain poorly understood. Murine pulmonary models of infection were therefore employed to assess and compare dissemination and pathology and to elucidate the host immune response to infection with the highly virulent Type A F. tularensis strain Schu4 versus the less virulent Type B live vaccine strain (LVS). We found that dissemination and pathology in the spleen was significantly greater in mice infected with F. tularensis Schu4 compared to mice infected with F. tularensis LVS. Using gene expression rofiling to compare the response to infection with the two F. tularensis strains, we found that there were significant differences in the expression of genes involved in the apoptosis pathway, antigen processing and presentation pathways, and inflammatory response pathways in mice infected with Schu4 when compared to LVS. These transcriptional differences coincided with marked differences in dissemination and severity of organ lesions in mice infected with the Schu4 and LVS strains. Therefore, these findings indicate that altered apoptosis, antigen presentation and production of inflammatory mediators explain the differences in pathogenicity of F. tularensis Schu4 and LVS

Comparative review of F. tularensis and F. novicida

Francisella tularensis is the causative agent of the acute disease tularemia. Due to its extreme infectivity and ability to cause disease upon inhalation, F. tularensis has been classified as a biothreat agent. Two subspecies of F. tularensis, tularensis and holarctica, are responsible for tularemia in humans. In comparison, the closely related species F. novicida very rarely causes human illness and cases that do occur are associated with patients who are immune compromised or have other underlying health problems. Virulence between F. tularensis and F. novicida also differs in laboratory animals. Despite this varying capacity to cause disease, the two species share ~97% nucleotide identity, with F. novicida commonly used as a laboratory surrogate for F. tularensis. As the F. novicida U112 strain is exempt from U.S. select agent regulations research studies can be carried out in non-registered laboratories lacking specialized containment facilities required for work with virulent F. tularensis strains. This review is designed to highlight phenotypic (clinical, ecological, virulence and pathogenic) and genomic differences between F. tularensis and F. novicida that warrant maintaining F. novicida and F. tularensis as separate species. Standardized nomenclature for F. novicida is critical for accurate interpretation of experimental results, limiting clinical confusion between F. novicida and F. tularensis and ensuring treatment efficacy studies utilize virulent F. tularensis strains

The Ly49 gene family. A brief guide to the nomenclature, genetics, and role in intracellular infection.

Understanding the Ly49 gene family can be challenging in terms of nomenclature and genetic organization. The Ly49 gene family has two major gene nomenclature systems, Ly49 and Killer Cell Lectin-like Receptor subfamily A (klra). Mice from different strains have varying numbers of these genes with strain specific allelic variants, duplications, deletions, and pseudogene sequences. Some members activate NK lymphocytes, invariant NKT lymphocytes and γδ T lymphocytes while others inhibit killing activity. One molecule, Ly49Q, is not found on NK cells at all, rather is expressed only on myeloid cells. There is growing evidence that these receptors may regulate not just the immune response to viruses, but other intracellular pathogens as well. Thus, this review's primary goal is to provide a guide for researchers first encountering the Ly49 gene family and a foundation for future studies on the role that these gene products play in the immune response, particularly the response to intracellular viral and bacterial pathogens

Solar Power Can Substantially Prolong Maximum Achievable Airtime of Quadcopter Drones

10.1002/advs.202001497Advanced Science720200149

Cave air and dripwater variability in Cathedral Caverns, Alabama

Monthly monitoring of dripwater (δ18O, δD, [DIC], δ13CDIC, and pH) and air (pCO2 and δ13CCO2) chemistry from within Cathedral Caverns (Grant, AL) was conducted for 12 months (January 2015-December 2015) to better characterize the factors influencing deposition and δ18O chemistry of speleothems within the cave. Cave dripwater (δ18O and δD) isotope values for the Southeast, US are thought to be consistent with a yearly average. Cave monitoring of Cathedral Caverns, however, indicates that dripwater values are biased towards the winter season. This winter signal is emphasized through the study of the cave air pCO2, which shows a maximum during the month of October (7691 ppmV) and minimums during the colder, winter months. The max pCO2 value indicates that less CO2 is degassing from the dripwater during the hot summer months while during the colder winter months, more CO2 is degassed leaving less [DIC] to remain in the dripwater and more potential calcite deposition onto the stalagmite. The [DIC] and δ13CDIC which range from 0.6 to 6.0 mM and -4.7 to -14.7‰, respectively, show that [DIC] is at a maximum and δ13CDIC is 13C-depleted during summer months. These results indicate that the paleoclimate record in Cathedral Cavern’s speleothems and possibly most SE U.S. caves is biased towards a winter climatic signal. This conclusion is supported by: (i) a strong coupling between the timing of karst aquifer recharge (winter) and increased dripwater flow rates, (ii) cave dripwater δ18O (-5.7‰ (±0.2)) and δD (-32.1‰ (±2.6)) being similar to winter rainwater (-5.1‰ (±1.4) for δ18O and -27.8‰ (±15.1) for δD) collected at nearby Tuscaloosa, AL, and (iii) more favorable chemical conditions for calcite deposition to occur during winter months. These data illustrate that seasonal cave air exchange with the outside atmosphere is an important control on cave-specific periods of enhanced calcite deposition as well as the effect on the chemistry of dissolved inorganic carbon within the dripwater. This work demonstrates the utility of monitoring dripwater chemistry before conducting on paleoclimate reconstructions and furthermore, serves as a precursor for paleoclimate reconstruction of δ18O in speleothems from Cathedral Caverns. (Published By University of Alabama Libraries

Plasmid based protein composition of <i>B</i>. <i>mayonii</i> in comparison to 4 other Bbsl genospecies and 1 RF <i>Borrelia</i> species.

<p>The mean amino acid identity is indicated for proteins present on each of the 14 <i>B</i>. <i>mayonii</i> plasmids. Comparisons are to protein databases constructed for <i>B</i>. <i>burgdorferi</i> (B.b.s.s.; green), <i>B</i>. <i>garinii</i> (B.g.; blue), <i>B</i>. <i>afzelii</i> (B. a.; red), <i>B</i>. <i>bissettii</i> (B.b.; yellow), and <i>B</i>. <i>miyamotoi</i> (B.m.; grey).</p