Transcriptome analysis of the reproduction of silkworm (Bombyx mori) under dimethoate stress.

Dimethoate (DMT) is an organophosphorus pesticide which is widely used to prevent and control agricultural diseases and pests. But it also remains in crops and the environment, affecting other non-target organisms. Existing research mainly focuses on aquatic invertebrates, and research on terrestrial invertebrates is still relatively weak. This study selected the lepidopteran model insect silkworm (Bombyx mori) as the research object and revealed the influence of DMT on the reproduction of silkworms. This study used digital gene expression (DGE) and RT-qPCR analysis to compare gene expression changes in eggs laid by silkworms under the exposure of DMT (200 mg/L). A total of 320 differential genes were detected, of which 211 genes were up-regulated and 109 genes were down-regulated. The GO enrichment analysis bar graph shows those differential genes enriched in the BP's metabolic process, cellular process, CC's membrane part, cell, MF's catalytic activity, binding. KEGG enrichment analysis showed more differential genes enriched in signal transduction, endocrine system, cancers: Overview pathway. The results showed that the differential genes were mainly concentrated on promoting trehalase transporter genes, stress response-related genes, zinc finger protein genes, epidermal protein genes, and 5-HT pathway-related genes. The results of this study will provide important gene sequence information for insect toxicology studies, and also clarify the mechanism of influence of DMT on silkworm reproduction at the transcription level.

The physiological and toxicological effects of antibiotics on an interspecies insect model.

Silkworm (Bombyx mori L.) has a clear genetic background, parts of which are highly homologous to certain genes related to human hereditary diseases. Thus, the species presents an excellent interspecies model for drug screening and microbe-host interaction studies. Chloramphenicol (CAM) and vancomycin (VCM) are antibiotics commonly used to treat specific bacterial infections in medical care, animal husbandry, and agriculture. However, inappropriate dosages and prolonged therapy increase their risk of toxicity. In this work, we investigated the physiological and toxicological responses of silkworm to combined oral administration of CAM and VCM. Results showed that antibiotics promote the feeding behavior of silkworm and significantly reduce (P < 0.05) intestinal cultivable bacterial counts. Moreover, antibiotics decreased the antioxidant enzyme activities of superoxide dismutase, catalase, glutathione S-transferase, and thioredoxin reductase and caused oxidative damage to the silkworm intestine; the degree of damage was confirmed by histopathology analysis. The gene expression levels of antimicrobial peptides (attacin, lysozyme, and cecropins) were also perturbed by antibiotics. After antibiotic exposure, 16S rRNA metagenomic sequencing revealed increases in the relative abundance of Sphingobium, Burkholderia, Barnesiella, Bacteroides, Bradyrhizobium, Acinetobacter, Phenylobacterium, Plesiomonas, Escherichia/Shigella, and unclassified bacteria, as well as a reduction of Enterococcus. The metabolic and functional profiles of intestinal microbiota, particularly metabolic processes, such as energy, cofactors and vitamins, lipid, amino acid, and carbohydrate metabolisms, changed after antibiotic exposure. In conclusion, our findings reveal that antibiotics exert substantial effects on silkworm. The present study may promote the applications of silkworm as an interspecies model in the medical and pharmaceutical fields.

An M29 Aminopeptidase from Listeria Monocytogenes Contributes to In Vitro Bacterial Growth but not to Intracellular Infection.

Aminopeptidases that catalyze the removal of N-terminal residues from polypeptides or proteins are crucial for physiological processes. Here, we explore the biological functions of an M29 family aminopeptidase II from Listeria monocytogenes (LmAmpII). We show that LmAmpII contains a conserved catalytic motif (EEHYHD) that is essential for its enzymatic activity and LmAmpII has a substrate preference for arginine and leucine. Studies on biological roles indicate that LmAmpII is required for in vitro growth in a chemically defined medium for optimal growth of L. monocytogenes but is not required for bacterial intracellular infection in epithelial cells and macrophages, as well as cell-to-cell spreading in fibroblasts. Moreover, LmAmpII is found as dispensable for bacterial pathogenicity in mice. Taken together, we conclude that LmAmpII, an M29 family aminopeptidase, can efficiently hydrolyze a wide range of substrates and is required for in vitro bacterial growth, which lays a foundation for in-depth investigations of aminopeptidases as potential targets to defend Listeria infection.

Impact of Al-based coagulants on the formation of aerobic granules: Comparison between poly aluminum chloride (PAC) and aluminum sulfate (AS).

As widely used Al-based coagulants, poly aluminum chloride (PAC) and aluminum sulfate (AS) were adopted in a short term at the start-up stage (from 10th to 16th) to enhance the formation of aerobic granules, and their effects on aerobic granulation were elucidated. The results suggested that both PAC and AS facilitated the granulation by improving the physicochemical properties of sludge. The reactor performance in pollutant removal was also enhanced. Specifically, in terms of extracellular polymeric substances (EPS), PAC dosing mainly stimulated the production of loosely bound EPS (LB-EPS), whereas more tightly bound EPS (TB-EPS) were secreted with the presence of AS. Based on the elemental analysis, polymeric Al hydrolyzed from PAC mainly worked on the exterior of microbial aggregates, and thus the attached aluminum in granules was gradually eliminated by ion exchange and hydraulic shear force. In contrast, the aluminum species in AS hydrolyzed into monomeric and oligomeric Al, and thus could diffuse into the interior of microbial aggregates and eventually created an "Al-core" in the granules. Overall, the present study describes the AGS formation with Al-based coagulants and the mechanisms of PAC- and AS-enhanced aerobic granulation.

Flagellar Basal Body Structural Proteins FlhB, FliM, and FliY Are Required for Flagellar-Associated Protein Expression in Listeria monocytogenes.

Listeria monocytogenes is a food-associated bacterium that is responsible for food-related illnesses worldwide. In the L. monocytogenes EGD-e genome, FlhB, FliM, and FliY (encoded by lmo0679, lmo0699, and lmo0700, respectively) are annotated as putative flagella biosynthesis factors, but their functions remain unknown. To explore whether FlhB, FliM, and FliY are involved in Listeria flagella synthesis, we constructed flhB, fliM, fliY, and other flagellar-related gene deletion mutants using a homologous recombination strategy. Then, we analyzed the motility, flagella synthesis, and protein expression of these mutant strains. Motility and flagella synthesis were completely abolished in the absence of flhB, fliM, or fliY. These impaired phenotypes were fully restored in the complemented strains CΔflhB, CΔfliM, and CΔfliY. The transcriptional levels of flagellar-related genes, including flaA, fliM, fliY, lmo0695, lmo0698, fliI, and fliS, were downregulated markedly in the absence of flhB, fliM, or fliY. Deletion of flhB resulted in the complete abolishment of FlaA expression, while it decreased FliM and FliY expression. The expression of FlaA was abolished completely in the absence of fliM or fliY. No significant changes were found in the expression of FlhF and two flagella synthesis regulatory factors, MogR and GmaR. We demonstrate for the first time that FlhB, FliM, and FliY not only mediate Listeria motility, but also are involved in regulating flagella synthesis. This study provides novel insights that increase our understanding of the roles played by FlhB, FliM, and FliY in the flagellar type III secretion system in L. monocytogenes.

Carboxyl-Terminal Residues N478 and V479 Required for the Cytolytic Activity of Listeriolysin O Play a Critical Role in Listeria monocytogenes Pathogenicity.

Listeria monocytogenes is a facultative intracellular pathogen that secretes the cytolysin listeriolysin O (LLO), which enables the bacteria to cross the phagosomal membrane. L. monocytogenes regulates LLO activity in the phagosome and minimizes its activity in the host cytosol. Mutants that fail to compartmentalize LLO activity are cytotoxic and have attenuated virulence. Here, we showed that residues N478 and V479 of LLO are required for LLO hemolytic activity and bacterial virulence. A single N478A mutation (LLON478A) significantly increased the hemolytic activity of LLO at a neutral pH, while no difference was observed at the optimum acidic pH, compared with wild-type LLO. Conversely, the mutant LLOV479A exhibited lower hemolytic activity at the acidic pH, but not at the neutral pH. The double mutant LLON478AV479A showed a greater decrease in hemolytic activity at both the acidic and neutral pHs. Interestingly, strains producing LLON478A or LLOV479A lysed erythrocytes similarly to the wild-type strain. Surprisingly, bacteria-secreting LLON478AV479A had barely detectable hemolytic activity, but exhibited host cell cytotoxicity, escaped from the phagosome, grew intracellularly, and spread cell-to-cell with the same efficiency as the wild-type strain, but were highly attenuated in virulence in mice. These data demonstrate that these two residues are required for LLO hemolytic activity and pathogenicity in mice, but not for escape from the phagosome and cell-to-cell spreading. The finding that the nearly non-hemolytic LLON478AV479A mutant grew intracellularly indicates that mutagenesis of a virulence determinant is a novel approach for the development of live vaccine strains.

Introduction of poly[(2-acryloyloxyethyl trimethyl ammonium chloride)-co-(acrylic acid)] branches onto starch for cotton warp sizing.

An attempt has been made to reveal the effect of amphoteric poly(2-acryloyloxyethyl trimethyl ammonium chloride-co-acrylic acid) [P(ATAC-co-AA)] branches grafted onto the backbones of starch upon the adhesion-to-cotton, film properties, and desizability of maize starch for cotton warp sizing. Starch-g-poly[(2-acryloyloxyethyl trimethyl ammonium chloride)-co-(acrylic acid) [S-g-P(ATAC-co-AA)] was prepared by the graft copolymerization of 2-acryloyloxyethyl trimethyl ammonium chloride (ATAC) and acrylic acid (AA) with acid-converted starch (ACS) in aqueous medium using Fe(2+)-H2O2 initiator. The adhesion was evaluated in term of bonding strength according to the FZ/T 15001-2008 whereas the film properties considered included tensile strength, work and percentage elongation at break. The evaluation was undertaken through the comparison of S-g-P(ATAC-co-AA) with ACS, starch-g-poly(acrylic acid), and starch-g-poly(2-acryloyloxyethyl trimethyl ammonium chloride). It was found that the amphoteric branch was able to significantly improve the adhesion and mitigate the brittleness of starch film. Zeta potential of cooked S-g-P(ATAC-co-AA) paste, depending on the mole ratio of ATAC to AA units on P(ATAC-co-AA) branches, had substantial effect on the adhesion and desizability. Increasing the mole ratio raised the potential, which favored the adhesion but disfavored the removal of S-g-P(ATAC-co-AA) from sized cotton warps. Electroneutral S-g-P(ATAC-co-AA) was superior to negatively grafted starch in adhesion and to positively grafted starch in desizability. Generally, it showed better sizing property than ACS, starch-g-poly(acrylic acid), and starch-g-poly(2-acryloyloxyethyl trimethyl ammonium chloride), and had potential in the application of cotton warp sizing.

Occurrence and potential health risk of Cryptosporidium and Giardia in the Three Gorges Reservoir, China.

The Three Gorges Reservoir (TGR) is the biggest lake in the world and a major water source in China. There is no information about occurrence and impact of Cryptosporidium and Giardia on the aquatic ecosystem. 61 surface water samples from 23 monitoring sites and 5 treated effluent samples were collected and analyzed. Cryptosporidium oocysts and Giardia cysts were found, respectively, in 86.4% and 65.2% of a total of 66 water samples, with high concentrations in treated effluent. The mean percent recovery was 29.14% for oocysts and 34.86% for cysts. A seasonal pattern was observed, with positive samples for Cryptosporidium more frequent in flood period and positive samples for Giardia more frequent in impounding period. Counts of enterococci, fecal coliforms and total coliforms, and turbidity were significantly associated with Cryptosporidium concentration in backwater (water in a main river which is backed up by the Three Gorges Dam) areas of tributaries but not Giardia. High associations were also found between oocyst and cyst in backwater areas of tributaries and cities. The risks of infection and illness due to water consumption in four different exposure routes were estimated. The results showed that swimming in the TGR has the highest infection risk with 1.39 × 10(-3) per time (95% confidence interval (CI): 0.05-600.3 × 10(-5)) for Cryptosporidium and 2.08 × 10(-4) per time (95% CI: 0.05-878.87 × 10(-6)) for Giardia, while directly drinking unboiled tap water treated with the conventional process has the highest morbidity with 524.98 per 100,000 population per year (95% CI: 10.35-2040.26) for Cryptosporidium and 5.89 per 100,000 population per year (95% CI: 0.08-22.67) for Giardia. This study provides new useful information for drinking water plants, health care workers and managers to improve the safety of tap water and deduce the risk of surface water contamination in China.