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In this work, an ecofriendly approach for biogenic production of copper oxide nanoparticles (CuO-NPs) was proposed by utilizing the Bacopa monnieri leaf extract as a reducing and stabilizing agent. The synthesis of CuO-NPs was instantly confirmed by a shift in the color of the copper solution from blue to dark gray. The use of UV−visible spectroscopy revealed a strong narrow peak at 535 nm, confirming the existence of monoclinic-shaped nanoparticles. The average size of CuO-NPs was 34.4 nm, according to scanning electron microscopy and transmission electron microscopy studies. The pristine crystalline nature of CuO-NPs was confirmed by X-ray diffraction. The monoclinic form of CuO-NPs with a crystallite size of 22 nm was determined by the sharp narrow peaks corresponding to 273, 541, 698, 684, and 366 Bragg's planes at different 2θ values. The presence of different reducing metabolites on the surface of CuO was shown by Fourier transform infrared analysis. The biological efficacy of CuO-NPs was tested against Helicobacter felis, Helicobacter suis, Helicobacter salomonis. and Helicobacter bizzozeronii. H. suis was the most susceptible strain with an inhibition zone of 15.84 ± 0.89 mm at 5 mg/mL of NPs, while the most tolerant strain was H. bizzozeronii with a 13.11 ± 0.83 mm of inhibition zone. In in vivo analgesic activity, CuO-NPs showed superior efficiency compared to controls. The maximum latency time observed was 7.14 ± 0.12 s at a dose level of 400 mg/kg after 90 min, followed by 5.21 ± 0.29 s at 400 mg/kg after 60 min, demonstrating 65 and 61% of analgesia, respectively. Diclofenac sodium was used as a standard with a latency time of 8.6 ± 0.23 s. The results observed in the rat paw edema assays showed a significant inhibitory activity of the plant-mediated CuO-NPs. The percentage inhibition of edema was 74% after 48 h for the group treated with CuO-NPs compared to the control group treated with diclofenac (100 mg/kg) with 24% edema inhibition. The solution of CuO-NPs produced 82% inhibition of edema after 21 days when compared with that of the standard drug diclofenac (73%). CuO-NPs vividly lowered glucose levels in STZ-induced diabetic mice, according to our findings. Blood glucose levels were reduced by about 33.66 and 32.19% in CuO-NP and (CuO-NP + insulin) groups of mice, respectively. From the abovementioned calculations, we can easily conclude that B. monnieri-synthesized CuO-NPs will be a potential antibacterial, anti-diabetic, and anti-inflammatory agent on in vivo and in vitro basis.

The main purpose of this study is to provide essential information regarding the molecular basis of insecticide resistance and to report candidate genes which are responsible for resistance in insects/pests. There are two basic resistance mechanisms existing in pests, i.e., target site resistance and metabolic resistance. During resistance of target site, the specific binding site of an insecticide is modified (mutated) and/or lost, which makes the target site incompatible for activation. Mutation occurs in most common pest (Myzus persicae, Musca domestica and Drosophila melanogaster) target regions, i.e., subunits like nicotinic acetylene choline receptors (nAChRs), knock-down resistance (KDR) etc. Due to these mutations, insecticides are unable to bind into the target region, resulting in loss of binding affinity. Furthermore, in metabolic resistance over production of enzymes occurs which break down (detoxify) insecticides and resulting resistance of pests. The amplification of metabolic enzymes, i.e., Cytochromes p450 monooxygenase, hydrolyses, and Glutathione S-transferase play a central role in evolving metabolic resistance. Various successful approaches are used to combat pests resistance such as insecticides, bio-pesticides and biological control agents. However, some of these strategies have certain limitations such as contamination of the environment, while others possess a low capacity in management of pests. Recent studies have highlighted some novel mechanisms of insecticide resistance that are part of the ongoing efforts to define the molecular basis of insecticide resistance in insect species.

Health and environmental problems arising from metals present in the aquatic ecosystem are very well known. The present study investigated toxicological effects of LC15 of metals such as copper, chromium, and lead for 24, 48, 72, and 96 h on hematological indices, RBC nucleus and cell morphology, and gill and muscle tissues of grass carp (Ctenopharyngodon idella). Experimental dose concentrations of copper were 1.5, 1.4, 1.2, and 1 mgL−1. Similarly, dose concentrations of chromium were 25.5, 22.5, 20, and 18 mgL−1 while those of lead were 250, 235, 225, and 216 mgL−1, respectively. Maximum decrease in the concentration of Hb, RBCs, and monocytes was observed against chromium, while maximum increase in the concentration of lymphocytes was reported against lead. Abnormalities such as single and double micronuclei, deformed nucleus, nuclear shift, irregular nucleus, deformed cells, microcyte cells, and vacuolated and swollen cells were observed. Gill tissues absorbed maximum concentration of lead followed by chromium and copper. Muscle tissues also absorbed maximum concentration of lead followed by chromium and copper, respectively. Histological alterations such as epithelial lifting, interlamellar spaces, club gill filaments, gill bridging, curling filaments, swelling and fusion of cells, irregular cells, destruction of epithelial cells, cellular necrosis, and inflammatory cells were observed in gill tissues while inflammation and necrosis of muscle fibers, degeneration of muscle fibers, edema of muscle bundles, zig-zag of muscle fibers, and lesions were observed in muscle tissues of fish exposed with different doses of these heavy metals, indicating the toxicity of metals to aquatic fauna as well as to human being via food chain.

Effect of Trichoderma harzianum was investigated on plant growth and inhibitory activity against Phythium ultimum and Phytopthora capsici under laboratory and greenhouse conditions. Data under lab conditions revealed that mycelial growth of both pathogens were inhibited by T. harzianum in vitro. The effect of T. harzianum on different plant growth parameters was assessed in the presence of P. ultimum and P. capsici. Fresh and dry shoot weight was reduced by both fungal strains. The fresh shoot weight was decreased by 38.8 and 44.4% in case of P. capsici and P. ultimum, respectively. T. harzianum improved the overall plant growth in the presence of P. ultimum and P. capsici. Histopathological observation of P. ultimum and P. capsici infected tissue of the root clearly indicated that both severely affected the epidermis and vascular bundle of the host plant. T. harzianum reduced the size of lesions caused by the two pathogens. Observation of hyphae interaction of the T. harzianum with pathogens demonstrated that it inhibited the entry of both pathogens to the vascular bundle of the host tissue. Furthermore, no effect was observed on the vascular bundle, pith and cortex of treated host plant inoculated with T. harzianum and pathogens.

Nanoparticles have long been known and their biomedical potent activities have proven that these can provide an alternative to other drugs. In the current study, copper oxide, nickel oxide and copper/nickel hybrid NPs were biosynthesized by using Curcuma longa root extracts as a reducing and capping agent, followed by characterization via UV-spectroscopy, Fourier transformed infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermo galvanometric analysis (TGA), and band gap. FTIR spectroscopy shows the availability of various functional groups and biomolecules such as carbohydrate, protein, polysaccharides, etc. The EDX peak confirmed that the elemental nickel and copper were present in large quantity in the analyzed sample. Scanning electron micrographs showed that the synthesized CuO-NPs and NiO-NPs were polyhedral uniform and homogeneous in morphology, while the copper/nickel hybrid NPs were well dispersed, spherical in shape, and uniform in size. TEM micrographs of CuO-NPs had 27.72 nm, NiO had 23.13 nm and, for their hybrid, the size was 17.38 nm, which was confirmed respectively. The CuO and NiO NPs possessed spherical- to multi-headed shapes, while their hybrid showed a complete spherical shape, small size, and polydispersed NPs. The XRD spectra revealed that the average particle size for CuO, NiO, and hybrid were 29.7 nm, 28 nm and 27 nm, respectively. Maximum anti-diabetic inhibition of (52.35 ± 0.76: CuO-NPs, 68.1 ± 0.93: NiO-NPs and 74.23 ± 0.42: Cu + Ni hybrids) for α-amylase and (39.25 ± 0.18 CuO-NPs, 52.35 ± 1.32: NiO-NPs and 62.32 ± 0.48: Cu + Ni hybrids) for α-glucosidase were calculated, respectively, at 400 µg/mL. The maximum antioxidants capacity was observed as 65.1 ± 0.83 μgAAE/mg for Cu-Ni hybrids, 58.39 ± 0.62 μgAAE/mg for NiO-NPs, and 52.2 ± 0.31 μgAAE/mg for CuO-NPs, respectively, at 400 μg/mL. The highest antibacterial activity of biosynthesized NPs was observed against P. aeuroginosa (28 ± 1.22) and P. vulgaris (25 ± 1.73) for Cu + Ni hybrids, respectively. Furthermore, the antibiotics were coated with NPs, and activity was noted. Significant anti-leishmanial activity of 60.5 ± 0.53 and 68.4 ± 0.59 for Cu + Ni hybrids; 53.2 ± 0.48 and 61.2 ± 0.44 for NiO-NPs; 49.1 ± 0.39 and 56.2 ± 0.45 for CuO-NPs at 400 μg/mL were recorded for promastigote and amastigotes, respectively. The biosynthesized NPs also showed significant anti-cancerous potential against HepG2 cell lines. It was concluded from the study that NPs are potential agents to be used as an alternative to antimicrobial agents.

The seasonal effect on haematology and body composition of Rohu and Mrigal carp were evaluated. Fifty-four fish of each species (Rohu length and weight 28.00±0.34 cm and 385±3.40 g; Mrigal carp length and weight 29.48±0.24 cm and 393±5.48 g) were collected from the Dera Ismail Khan. The values of WBCs (9.31 and 8.41×106 mm-3), RBCs (2.37 and 2.12×106 mm-3), Hb (9.58 and 8.78) and HCT (38.06 and 36.04 %) of Rohu and Mrigal carp were higher in summer whereas declined in winter (P<0.05). The MCV, MCH and MCHC of both species were higher (P<0.05) in winter, and decreased during summer. The moisture content of both Rohu and Mrigal carp was higher during winter followed by spring and lower in summer season. Lipid and protein content of both species were higher (P<0.05) in summer and lower in winter. The moisture content, proteins and lipid were found higher in Rohu than Mrigal carp. According to the findings, it was concluded that the water quality parameters vary seasonally which in turn impacts on body physiology of fish species.

Poultry meat serves as an important source of protein having different essential amino acids but is associated with various infectious bacteria. The aim of this study was to find out the prevalence and isolation of Salmonella from poultry chicken and to check it against antibiotic. About 150 samples were collected from different areas of District Swat. The samples were of three type, i.e. fresh raw meat, cloacal swamp sample from slaughter houses and cutting board cloacal swab samples. Based on temperature fluctuation, the sample collection sites were categorized into three regions, i.e. colder, moderate and warm regions. The samples were cultured on different media, e.g. Nutrient Agar (NA), MacConkey Agar (MCA), Deoxycholate Citrate Agar (DCA) and Salmonella-Shigella Agar (S.S). The isolated bacteria were identified after gram staining and Biochemical tests including Indole (I),Methyl Red (M), Vogus Proskeur (Vi), Citrate (C), Urease and Triple Sugar Iron (TSI) Test etc. For the Identification Burjey's Manual was followed. Isolated bacteria included Salmonella 22%, E.coli 20.66%, Klebsiella 15.3 %, Proteus 11.3 %, Pseudomonas 8.6 % and Shigella 7.3%. Raw meat of poultry chicken had about 18% prevalence, slaughter house had 26%, while cutting boards had 22% prevalence of Salmonella. Salmonella isolated from all the sources was resistant to different antibiotics including tetracycline (89%), neomycin (80%), ampicillin (75%) and novobiocin (74%). It was also revealed in present investigation that salmonella was sensitive to ceftriaxone (100%), cephradine (100%), piperacillin-tazobactam (94%) and cefepime (90%).It is concluded that Salmonella is frequently present in chicken and is a major source of Salmonellosis.