The Effect of Lactococcus lactis subsp. lactis PTCC 1403 on the Growth Performance,Digestive Enzymes Activity,Antioxidative Status,Immune Response,and Disease Resistance of Rainbow Trout (Oncorhynchus mykiss)

The effect of Lactococcus lactis subsp. lactis strain PTCC 1403 as a potential probiotic was investigated on the growth, hematobiochemical, immune responses, and resistance to Yersinia ruckeri infection in rainbow trout. A total of 240 fish were distributed into 12 fiberglass tanks representing four groups (× 3 replicates). Each tank was stocked with 20 fish (average initial weight: 11.81 ± 0.32 g) and fed L. lactis subsp. lactis PTCC 1403 at 0 (control, T0), 1 × 10⁹ (T1), 2 × 10⁹ (T2), and 3 × 10⁹ (T3) CFU/g feed for 8 weeks. The results showed enhanced protein efficiency ratio and reduced feed conversion ratio in the fish-fed T2 diet. Further, fish-fed T2 and T3 diets showed a significantly higher survival rate than the control (p < 0.05). Trypsin, lipase, and protease activities were increased in fish-fed L. lactis subsp. lactis PTCC 1403 compared to the control (p < 0.05). Fish fed with a T2 diet showed significantly (p < 0.05) lower glucose content than other groups. The blood lysozyme activity and IgM showed significantly (p < 0.05) higher values in fish-fed T2 and T3 diets than in other groups. The antioxidative responses were increased in fish-fed T2 and T3 diets (p < 0.05). After 7 days post-Y. ruckeri challenge, the cumulative mortality rate showed the lowest value in fish fed with T1 and T2 diets, while the highest value was recorded in the control group. In conclusion, the results revealed beneficial effects of L. lactis subsp. lactis PTCC 1403 on the feed efficiency, immune response, and resistance to Y. ruckeri infection in rainbow trout.

     

Th1/Th2 cytometric bead array can discriminate cytokine secretion from endogenously activated cells in pulmonary disease, recent and remote infection in tuberculosis

Differential T cell trafficking through the blood compartment towards infected foci may be occurring in different stages of tuberculosis disease and infection. The aim of the present study was to identify cytokine signatures in the blood compartment in tuberculosis patients with pulmonary disease (PTB=19), recently exposed household contacts (HC=27) and nonexposed community controls (EC=37). Diluted (1:10) whole blood was cultured for 2 days and cytokine secretion was assessed using Cytometric Bead Array (Th1/Th2 kit II; BD Biosciences) which included IL-2, TNF-α, IFN-γ (Type1/T1), IL-4, IL-6 and IL-10 (Type2/T2). All T1/T2 cytokines were elevated in PTB (AUROC>0.9) while HC showed selective elevation of IL-6 (AUROC>0.7) compared to EC. Principal component analysis (PCA) extracted two groupings with Eigen values >1; IL-6 separated into the second component for PTB, HC and EC. After rotation, IFN-γ was correlated with the first component for PTB and EC and the second component for HC indicating an absence of T1/T2 dichotomy. Therefore endogenous cytokine signatures may indicate differential T cell trafficking in different stages of tuberculosis infection and disease.     

Overexpression of proinflammatory TLR-2-signalling lipoproteins in hypervirulent mycobacterial variants

Changes in the cell envelope composition of mycobacteria cause major changes in cytokine profiles of infected antigen presenting cells. We describe here the modulation of inflammatory responses by Mycobacterium abscessus, an emerging pathogen in cystic fibrosis. M. abscessus is able to switch from a smooth (S) to a rough (R) morphotype by the loss of a surface glycopeptidolipid. R variants are associated with severe clinical forms and a 'hyper-proinflammatory' response in ex vivo and in vivo models. Using partitioning of cell surface components we found that a complex fraction, more abundant in R variants than in S variants, made a major contribution to the TLR-2-dependent hyper-proinflammatory response induced by R variants. Lipoproteins were the main TLR-2 agonists in this fraction, consistent with the larger amounts of 16 lipoproteins in cell surface extracts from R variants; 15 out of 16 being more strongly induced in R variant than in S variant. Genetic interruption of glycopeptidolipid pathway in wild-type S variant resulted in R phenotype with similar induction of lipoprotein genes. In conclusion, R morphotype in M. abscessus is associated with increased synthesis/exposure at the cell surface of lipoproteins, these changes profoundly modifying the innate immune response through TLR-2-dependent mechanisms.     

Analytical Performance of the Roche LightCycler? Mycobacterium Detection Kit for the Diagnosis of Clinically Important Mycobacterial Species

Background

The LightCycler® Mycobacterium Detection Kit based on real-time PCR technology for the detection of Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium kansasii was recently developed. This study evaluated its analytical sensitivity, specificity and reproducibility.

Methodology/Principal Findings

Plasmid standards were prepared and used to determine the limit of detection. The assay was also performed against organisms other than mycobacteria, other mycobacterial strains and interfering substances to exclude cross-reactivity and interference. Reference standards were prepared and tested to assess the assay''s reproducibility. All PCR assays were performed using the LightCycler® 2.0 Instrument. The detection limit for M. tuberculosis was 28 copies per microlitre. Neither cross-reactivity nor interference occurred with non-mycobacterial organisms and substances tested. Overall reproducibility for consecutive measurements, run-to-run, lot-to-lot, day-to-day and laboratory-to-laboratory achieved a coefficient of variance of less than two percent.

Significance

The LightCycler® Mycobacterium Detection kit has shown to be a robust and accurate assay with the potential to be used as a rapid TB diagnostic test.     

Role of organic soil amendments with some non-conventional plant additives on the growth of eggplant and their role against Meloidogyne incognita infection

The effects of four waste residues from castor (Ricinus communis L.), rocket (Eruca sativa Mill.), linseed (Linum usitatissimum L.) and wheat germ (Triticum aestivum L.) crops oil extraction as soil amendments at three rates (on base lower rate, recommended rate and higher rate), in comparison with the nematicide Nemacur 10% G were evaluated in greenhouse conditions (25 ± 5°C) at the National Research Center, Egypt, during two successive seasons on the physiological influence on the eggplant and on the infection by the root-knot nematode Meloidogyne incognita. All the tested treatments significantly reduced the numbers of juveniles in soil or in roots, number of galls, egg-masses, gall and egg-mass indices and the rate of nematode build-up. Significant differences in the nematode stages were found within and between treatments. The percentage reduction in the nematode stages was greater with the use of wheat germ mill residues (WGMR) compound followed by castor seed mill residues (CAMR) compound, rocket seed mill residues (RSMR) and Nemacur 10% G. The application of linseed mill residues (LSMR) was the least effective in reducing the nematode stages. Regarding infected plants, all the evaluated amendments achieved significant increases in the almost shoot and root growth variables, total contents of photosynthetic pigments, phenolics and carbohydrates when compared with nematode inoculated and untreated plants. As for healthy plants, it is clear that all the doses of WGMR compound and the highest doses (3.75%, w/w) of the other additives had pronounced effect on the growth parameters and phenolic content of dry leaves of the eggplant. In addition, all the treatments increased photosynthetic pigments and carbohydrates content of the eggplant. These results indicate that some seed mill residues may be used as natural nematicides in controlling M. incognita nematode and improving the growth and some chemical composition of the eggplant.     

Climate and vegetation structure determine plant diversity in Quercus ilex woodlands along an aridity and human-use gradient in Northern Algeria

We studied the influence of environmental factors relating to climate, soil and vegetation cover on total species richness, species richness of different life-forms and species composition of plant communities occurring in Quercus ilex woodlands, across a 450-km long transect in Northern Algeria constituting a gradient of aridity and human use. We sampled vegetation and collected environmental data in 81 10 m × 10 m plots in five zones representing the largest Q. ilex woodlands throughout the study area, analysing them within an a priori hypothesis framework with the use of Path Analysis. Changes in plant diversity were mainly influenced by environmental factors related to precipitation and temperature regimes, as well as by total plant cover. In particular, changes in species composition were determined by factors associated with the temperature regime through their influence on both woody and annual herbaceous plant richness, and by factors related to the precipitation regime through their influence on perennial herbaceous plant richness, likely due to the differential tolerances of these functional groups to cold and water stress. Our results emphasize the importance of differences in environmental adaptability of the most important life-forms with regard to explaining compositional change (beta diversity) along aridity gradients, and the mediator role of total plant cover in relation to the effects of soil conditions on plant diversity.     

An APETALA3 homolog controls both petal identity and floral meristem patterning in Nigella damascena L. (Ranunculaceae)

Flower architecture mutants provide a unique opportunity to address the genetic origin of flower diversity. Here we study a naturally occurring floral dimorphism in Nigella damascena (Ranunculaceae), involving replacement of the petals by numerous sepal‐like and chimeric sepal/stamen organs. We performed a comparative study of floral morphology and floral development, and characterized the expression of APETALA3 and PISTILLATA homologs in both morphs. Segregation analyses and gene silencing were used to determine the involvement of an APETALA3 paralog (NdAP3–3) in the floral dimorphism. We demonstrate that the complex floral dimorphism is controlled by a single locus, which perfectly co‐segregates with the NdAP3–3 gene. This gene is not expressed in the apetalous morph and exhibits a particular expression dynamic during early floral development in the petalous morph. NdAP3–3 silencing in petalous plants perfectly phenocopies the apetalous morph. Our results show that NdAP3–3 is fully responsible for the complex N. damascena floral dimorphism, suggesting that it plays a role not only in petal identity but also in meristem patterning, possibly through regulation of perianth organ number and the perianth/stamen boundary.