<it>Plasmodium yoelii </it>blood-stage primes macrophage-mediated innate immune response through modulation of toll-like receptor signalling

Abstract Background Toll-like receptors (TLRs) signalling is reported to be primed by the infection of human malaria parasite, Plasmodium falciparum. However, little is known about the regulation of macrophages TLR signalling by the infection of lethal or non-lethal strain of rodent malaria parasites. Methods BALB/c mice were infected with non-lethal strain Plasmodium yoelii 17XNL or lethal strain P. yoelii 17XL. Peritoneal macrophages were isolated to study its immune response to pRBC lysate, and TLRs (TLR2, TLR4, and TLR9) agonists, and the expression of TLRs and intracellular signalling molecules were also investigated by flow cytometry and semi-quantitive RT-PCR. Results The reactivity of peritoneal macrophages from the mice infected with lethal strain P. y 17XL or non-lethal strain P. y 17XNL were enhanced to pRBC lysate, and TLR2, TLR4, and TLR9 agonists at one, three and five days post-infection. Of all the tested TLRs, only TLR2 was up-regulated on peritoneal macrophages of mice infected with either strain. However, transcription of intracellular signalling molecules MyD88, IRAK-1, and TRAF-6 was significantly up-regulated in peritoneal macrophages from mice infected either with P. yoelii 17XL or P. yoelii 17XNL at one, three and five days post-infection. However, the enhanced TLRs response of macrophage from P. yoelii 17XNL-infected mice persisted for a much longer time than that from P. yoelii 17XL-infected mice. Conclusion Both P. yoelii 17XL and 17XNL strains could enhance the response of peritoneal macrophages to pRBC lysate and TLR agonists, through up-regulating the expression of TLR2 and intracellular signalling molecules MyD88, IRAK-1, and TRAF-6. In addition, prolonged high response of macrophage from P. yoelii 17XNL-infected mice might be associated with the more efficiently controlling of P. yoelii 17XNL growth in mice at early stage.</p

Effects of organic loading rates on the anaerobic co-digestion of fresh vinegar residue and pig manure: Focus on the performance and microbial communities

The 70 L mesophilic semi-continuous stirred tank reactor (semi-CSTR) for co-digestion of fresh vinegar residue (FVR) and pig manure (PM) was operated for 180 days to evaluate the behavior of process stability, inhibition and recovery, as well as the succession of microbial community structures with the increasing organic loading rates (OLRs). The maximum tolerable OLR for co-digestion was determined to be 5.0 g-VS/(L.d), achieving an average methane yield (MY) of 233.77 mL/g-VS. The feeding was paused for 7 days due to the accumulation of volatile fatty acids (VFAs), and then recovered at 5.5 g-VS/(L.d) with the maximum MY of 230.09 mL/g-VS. Meanwhile, the effect of OLRs on the microbial community was analyzed. It showed that there is a significant correlation between most of the major bacteria and VFA. PCA showed that stopping feeding and reducing OLR could change the bacterial community, but not archaeal community. The aceticlastic Methanosaeta was dominant at stable stage, and gradually replaced by the hydrogenotrophic methanogen, leading to the accumulation of acetate with increasing OLR. In the recovery stage, Methanosarcina became dominant to utilize the residual acetate. Due to the vigorous aceticlastic pathway of methanogenesis, the hydrogenotrophic pathway was depressed and the H2 pressure increased, causing the accumulation of propionate in a short time. With the relative abundance of Methanosarcina increasing constantly, the VFA except propionate decreased, suggesting that Methanosarcina transformed acetate and hydrogen into methane during the recovery stage.Supplementary Material_V4.do

Insight into Tar Formation Mechanism during Catalytic Pyrolysis of Biomass over Waste Aluminum Dross

Tar is one of major products from biomass pyrolysis. Its formation mechanism in a catalytic pyrolysis system comprising pine sawdust and waste aluminum dross (AD) is investigated with the aid of analytical methods including thermogravimetric analysis (TG), Nuclear Magnetic Resonance (NMR), electron paramagnetic resonance (EPR), and gas chromatography coupling with mass spectrometry (GC-MS). The results show that AD plays a vital role in cleavage of C-O bonds to enhance selective formation of furans, ketones, and phenols. The catalytic pyrolysis is initiated by active C-O-M intermediate formation that accelerates C-O bond cleavage and generates great amounts of free radicals to 1020 spins/g at 300-500 degrees C. Compared with pure pine pyrolysis, the percentage of glucosidic bonds from cellulose decreases from 14.00% to 9.66% at 500 degrees C; the etherified guaiacyl is more actively ruptured and disappears at 700 degrees C. Furans and ketones increase from 17.45% to 22.23% and 6.71% to 10.80% at 500 degrees C, respectively. Phenols increase from 66.75% to 71.57%. The preferential production of higher value-added products via catalytic pyrolysis between biomass and industrial wastes may bring new insight to the simultaneous valorization of agricultural, municipal, and industrial waste

Designing Multi-Stage 2 A/O-MBR Processes for a Higher Removal Rate of Pollution in Wastewater

Multi-stage A/O-MBR processes were designed to improve wastewater treatment efficiency; three different designs were carried out and compared in this study. The 2(A/O)-MBR process, i.e., with two sets of anoxic/oxic tanks in series, showed better effluent quality than A/O-MBR and 3(A/O)-MBR processes. The removal rates of COD, NH4+-N, TP and TN were 95.29%, 89.47%, 83.55% and 78.58%, respectively, complying satisfactorily with China's urban sewage treatment plant pollutant discharge standards. In terms of membrane fouling, the 3(A/O)-MBR process demonstrated the lowest fouling propensity. The microbial community structure in each bioreaction tank was analyzed, the results from which matched with the process efficiency and fouling behavior

A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation

Abstract The autosomal dominant form of polycystic kidney disease (ADPKD) is the most common hereditary disease that causes late-onset renal cyst development and end-stage renal disease. Preimplantation genetic testing for monogenic disease (PGT-M) has emerged as an effective strategy to prevent pathogenic mutation transmission rely on SNP linkage analysis between pedigree members. Yet, it remains challenging to establish reliable PGT-M methods for ADPKD cases or other monogenic diseases with de novo mutations or without a family history. Here we reported the application of long-read sequencing for direct haplotyping in a female patient with de novo PKD1 c.11,526 G > C mutation and successfully established the high-risk haplotype. Together with targeted short-read sequencing of SNPs for the couple and embryos, the carrier status for embryos was identified. A healthy baby was born without the PKD1 pathogenic mutation. Our PGT-M strategy based on long-read sequencing for direct haplotyping combined with targeted SNP haplotype can be widely applied to other monogenic disease carriers with de novo mutation