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This manuscript aims to 1) provide specific guidelines on PMM techniques in the setting of minimally invasive autopsy (MIA), both for pathologists collecting samples and for microbiologists advising pathologists and interpreting the results and 2) introduce standardization in PMM sampling at MIA. Post-mortem microbiology (PMM) is crucial to identify the causative organism in deaths due to infection. MIA including the use of post-mortem (PM) computed tomography (CT) and PM magnetic resonance imaging (MRI), is increasingly carried out as a complement or replacement for the traditional PM. In this setting, mirroring the traditional autopsy, PMM aims to detect infectious organisms causing sudden unexpected deaths; confirm clinically suspected but unproven infection; evaluate the efficacy of antimicrobial therapy; identify emergent pathogens; and recognize medical diagnostic errors. Meaningful interpretation of PMM results requires careful evaluation in the context of the clinical history, macroscopic and microscopic findings. These guidelines were developed by a multidisciplinary team with experts in various fields of microbiology and pathology on behalf of the ESGFOR (ESCMID – European Society of Clinical Microbiology and Infectious Diseases – Study Group of Forensic and Post-mortem Microbiology, in collaboration with the ESP -European Society of Pathology-) based on a literature search and the author’s expertise. Microbiological sampling methods for MIA are presented for various scenarios adults, children, developed and developing countries. Concordance between MIA and conventional invasive autopsy is substantial for children and adults and moderate for neonates and maternal deaths. Networking and closer collaboration among microbiologists and pathologists is vital to maximize the yield of PMM in MIA.Plant diseases significantly impact the global economy, and plant pathogenic microorganisms such as nematodes, viruses, bacteria, fungi, and viroids may be the etiology for most infectious diseases. In agriculture, the development of disease-free plants is an important strategy for the determination of the survival and productivity of plants in the field. This article reviews biosensor methods of disease detection that have been used effectively in other fields, and these methods could possibly transform the production methods of the agricultural industry. The precise identification of plant pathogens assists in the assessment of effective management steps for minimization of production loss. The new plant pathogen detection methods include evaluation of signs of disease, detection of cultured organisms, or direct examination of contaminated tissues through molecular and serological techniques. Laboratory-based approaches are costly and time-consuming and require specialized skills. The conclusions of this review also indicate that there is an urgent need for the establishment of a reliable, fast, accurate, responsive, and cost-effective testing method for the detection of field plants at early stages of growth. We also summarized new emerging biosensor technologies, including isothermal amplification, detection of nanomaterials, paper-based techniques, robotics, and lab-on-a-chip analytical devices. However, these constitute novelty in the research and development of approaches for the early diagnosis of pathogens in sustainable agriculture.Though having an economic and ecological impact on Marriott Lake management in Egypt, water hyacinth (Eichhornia crassipes) is an aquatic floating macrophyte with a known phytoremediation potential. Talazoparib cost In order to assess its remediation potential, pilot floating treatment wetlands (FTWs) with E. crassipes were built in duplicates to evaluate the removal of nutrients and heavy metals from the polluted lake water. The experimental design included units with different water depths (15, 25, and 35 cm; D15, D25, and D35, respectively) and plant coverage (90, 70, 50, and 0%; P90, P70, P50, and P0, respectively). The pilot FTWs were monitored over a 7-day operation cycle to identify the optimum combination of design (plant coverage, water depth) and operation (hydraulic retention time; HRT) parameters needed for maximum BOD5, TN, NH4-N, and TP removal. NH4-N removal reached 97.4% in the D25P50 unit after 3 days, BOD5 75% in the D15P90 after 3 days, TN 82% in the D25P70 after 4 days, and TP 84.2% in the D35P70 after 4 days. The open-water evaporation rate was higher than the evapotranspiration rate in the planted units, probably due to the warm climate of the study area. Metals were also sufficiently removed through bioaccumulation in plant tissues in the order of Fe > Pb > Cu > Ni (62.5%, 88.9%, 81.7%, and 80.4% for D25P50, D25P70, D25P50, and D25P90, respectively), while most of the assimilated metal mass was translocated to the plant roots. The biochemical composition of the plant tissue was significantly different between the shoot and root parts. Overall, the FTW with 70% E. crassipes coverage, 25-cm water depth, and an HRT of 3-5 days was identified as the optimum design for effective remediation of the polluted Marriott Lake in Egypt.Numerous active pharmaceutical ingredients (APIs) have been detected in various environmental matrices. Thus, their potential to elicit their toxic effect on non-target organisms is a growing concern, especially in the aquatic environment. This study aimed to investigate the potential toxicity of ibuprofen (IBU) at environmentally relevant concentration on the haematology and histology of the gill, liver, and kidney over 30 days. The 96-h acute toxicity data showed that IBU was moderately toxic to C. gariepinus with an LC50 value of 3.78 mg/L. After 15 and 30 days of exposure, there was a significant alteration in haematological indices in the treated fishes when compared to the control group. Throughout the experimental duration, the level of the mean corpuscular volume (MCV) and mean corpuscular haemoglobin (MCH) were consistently lower significantly, in contrast to the control group. IBU induced histopathological deformities in the gills, liver, and kidney of the exposed fishes, with alterations such as showing severe secondary lamella necrosis (SLN), epithelial lifting (EL), mild deformity of the secondary lamella (DSL), mild secondary lamella necrosis (MLN), and mild vascular congestion in the liver and kidney, respectively.