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Under the parent petrochemical industries, plastic industry is proliferating enormously over the past several years globally due to its advantages in terms of weight, robustness, expense, versatility, and durability. Due to the diversified consumer base representing varied climate zones, food habits, and standards of living, the generation and growth opportunities for the plastic industry in India are particularly distinct and humongous. The present work extensively reviews the Indian plastic industry with primary focus on the evolving technologies for plastic waste valorization encompassing their level of utilization, technology readiness, and progress achieved at R&D level. The study attempts to recognize different issues related to technology, recycling, policy, research, regulation that should be given attention to formulate an improved plastic waste management strategy in the region. Though significant shares of waste plastics in the country are processed by traditional practices, state-of-the-art technologies primarily plastic to oil conversion, in road making and in cement manufacturing, are being deployed at increasing rate. Action to tackle the problem of plastic contamination in India will need to adopt a pan India strategic consensus/concurrent approach for effective waste collection and segregation with active participation of urban local bodies, fixing the role of the informal sectors, investment for reliable technology adoption with skilled manpower for operation, adoption of circular economy schemes involving plastic waste co-processing, and providing support to work on R&D for better penetration of the proven plastic valorization options along with their environmental and social implications.

The non-ending needs of growing human population are being met by rapid industrialization and globalization, which have nowadays become an indispensable component of growth. Although these activities have led to phenomenal growth of the human civilization, at the same time, they have resulted in severe environmental pollution by discharge of highly toxic waste. This waste is severely detrimental not only for the environment but also for the health of the human population. Among different classes of pollutants, one being considered as one of the highly toxic ones is that of persistent organic pollutants (POPs). Advanced oxidation technologies (AOTs) play a major role in the degradation of pollutants by converting organic pollutants into CO 2 , H 2 O, and mineralized inorganic ions. AOTs include UV-based photocatalysis, ozonation, electrochemical oxidation, and Fenton and Fenton-like processes There are some difficulties and challenges associated with AOT, such as being highly capital intensive and high consumption of energy. To overcome these bottlenecks, photocatalytic degradation is a promising method that uses solar energy for the degradation of such pollutants. Photocatalysis is further classified into homogenous and heterogenous photocatalysis. As a part of heterogenous photocatalysis, semiconductor photocatalysts have received great attention; but because of their drawbacks such as the recombination of the electron/hole pair, low adsorption rate, and low surface area coverage, nanotechnology was considered for bringing a novel and enhanced remediation photocatalysis process. To this end, the designing of a more efficient photocatalyst by modifying morphology, composition, and structure and reducing toxicity is the need of the hour for the abatement of environmental pollutants. This review focuses on the degradation and removal of highly toxic persistent organic pollutants by using photocatalytic degradation with a detailed account of the various pollutants, their degradation mechanism, process shortcomings, remedial measures, and future prospects.

Some pathogens and toxins have the potential to be used as weapons of mass destruction and instigate population-based fear. Efforts to mitigate biothreat require development of efficient countermeasures which in turn relies on fast and accurate methods to detect the biological agents in a range of complex matrices including environmental and clinical samples. We report here an mass spectrometry (MS) based methodology, employing both targeted and shot-gun approaches for the verification of biological agents from the environmental samples. Our shot-gun methodology relied on tandem MS analysis of abundant peptides from the spiked samples, whereas, the targeted method was based on an extensive elucidation of marker proteins and unique peptides resulting in the generation of an inclusion list of masses reflecting relevant peptides for the unambiguous identification of nine bacterial species [listed as priority agents of bioterrorism by Centre for Disease Control and Prevention (CDC)] belonging to phylogenetically diverse genera. The marker peptides were elucidated by extensive literature mining, in silico analysis, and tandem MS (MS/MS) analysis of abundant proteins of the cultivated bacterial species in our laboratory. A combination of shot-gun MS/MS analysis and the targeted search using a panel of unique peptides is likely to provide unambiguous verification of biological agents at sub-species level, even with limited fractionation of crude protein extracts from environmental samples. The comprehensive list of peptides reflected in the inclusion list, makes a valuable resource for the multiplex analysis of select biothreat agents and further development of targeted MS/MS assays.

Species-specific wingbeat frequency of mosquitoes has already been shown to be useful in species identification. However, mosquito identification using their fundamental wingbeat frequency requires proper evaluation along with its morphological and ecological characters. An acoustic study was carried out on four species of laboratory reared mosquitoes Aedes albopictus, Culex quinquefasciatus, Anopheles crawfordi, and Armigeres subalbatus. However, a detailed study on wingbeat frequency and its variation at different points of the adult life stages was conducted for Ae. albopictus and Cx. quinquefasciatus . Recorded wingbeat beat frequency during the different point of adult life stages was analyzed using the Raven Pro 1.6.1 sound analysis software. Result showed that there was a significant difference in the fundamental frequency between four study species (F = 81.62; df  = 151; p  < 0.001). Wingbeat frequency of Ae. albopictus and Cx. quinquefasciatus observed to be low immediately after emergence from the pupal stage and gradually became peak during the swarming stage which is considered as the species’ fundamental frequency. These change in wingbeat frequency during the early adult stages leads to uncertainty in species identification based on the fundamental frequency. Swarming and pairing activities in Cx. quinquefasciatus and Ae. albopictus exclusively depends on the convergence between male first harmonics (M 1 ) and female second harmonics (F 2 ) of their fundamental frequency and make combined harmonic frequency at 1400–1500 Hz. Interestingly, this study observed that the frequency of adult male and early stages of female did not converge at the M 1 –F 2 harmonics, thereby preventing successful mating. It thus infers that the wingbeat frequency of active male and female have significant role in the selection of potential mates within the species.

Five IFA positive (including two qPCR positive) and 13 IFA negative patients had a history of domestic animal contact such as cattle, sheep, goat, dog or their residence situated near the abattoir [Table 1]. Laboratory definition and interpretation of acute QF[9] based on gold standard IFA is as follows: (i) IgM phase II + IgG phase II antibodies → acute QF; (ii) IgG phase II with or without IgG phase I → resolved past QF; and (iii) other combination viz., IgM/IgG phase II and/or IgM/IgG phase I → inconclusive, PCR to be performed. [...]the present study showed presence of QF in and around Puducherry. Authors thank the Indian Council of Medical Research (ICMR), New Delhi, for ad-hoc task force research project to the third author (SS) (30/3/41/2008/ECD-II), and to the Chairman, Vice-Chancellor, and Dean (Research and Allied Health Sciences) of Mahatma Gandhi Medical College and Research Institute, Puducherry, for providing financial assistance from Sri Balaji Vidyapeeth University Faculty Research Fund.

Some pathogenic microbes can be used for nefarious applications and instigate population-based fear. In a bio-threat scenario, rapid and accurate methods to detect biological agents in a wide range of complex environmental and clinical matrices, is of paramount importance for the implementation of mitigation protocols and medical countermeasures. This study describes targeted and shot-gun tandem MS based approaches for the verification of biological agents from the environmental samples. The marker proteins and peptides were elucidated by an exhaustive literature mining, in silico analysis of prioritized proteins, and MS/MS analysis of abundant proteins from selected bacterial species. For the shot-gun methodology, tandem MS analysis of abundant peptides was carried from spiked samples. The validation experiments employing a combination of shot-gun tandem MS analysis and a targeted search reported here is a proof of concept to show the applicability of the methodology for the unambiguous verification of biological agents at sub-species level, even with limited fractionation of crude protein extracts from environmental samples.

Background & objectives: Botulism, a potentially fatal paralytic illness, is caused by the botulinum neurotoxins (BoNTs) secreted by Clostridium botulinum. It is an obligate anaerobic, Gram-positive, spore-forming bacterium. BoNTs are classified into seven serotypes based on the serological properties. Among these seven serotypes, A, B, E and, rarely, F are responsible for human botulism. The present study was undertaken to develop an enzyme-linked immunosorbent assay (ELISA)-based detection system for the detection of BoNT/E. Methods: The synthetic gene coding the light chain of BoNT serotype E (BoNT/E LC) was constructed using the polymerase chain reaction primer overlapping method, cloned into pQE30UA vector and then transformed into Escherichia coli M15 host cells. Recombinant protein expression was optimized using different concentrations of isopropyl-β-D-1-thiogalactopyranoside (IPTG), different temperature and the rBoNT/E LC protein was purified in native conditions using affinity column chromatography. The purified recombinant protein was checked by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and further confirmed by western blot and matrix-assisted laser desorption ionization-tandem time-of-flight (MALDI-TOF). Polyclonal antibodies were generated against rBoNT/E LC using Freund's adjuvant in BALB/c mice and rabbit. Sandwich ELISA was optimized for the detection of rBoNT/E LC and native crude BoNT/E, and food matrix interference was tested. The developed antibodies were further evaluated for their specificity/cross-reactivity with BoNT serotypes and other bacterial toxins. Results: BoNT/E LC was successfully cloned, and the maximum expression was achieved in 16 h of post-induction using 0.5 mM IPTG concentration at 25°C. Polyclonal antibodies were generated in BALB/c mice and rabbit and the antibody titre was raised up to 128,000 after the 2nd booster dose. The developed polyclonal antibodies were highly specific and sensitive with a detection limit about 50 ng/ml for rBoNT/E LC and 2.5×10[3] MLD50 of native crude BoNT/E at a dilution of 1:3000 of mouse (capturing) and rabbit (revealing) antibodies. Further, different liquid, semisolid and solid food matrices were tested, and rBoNT/E LC was detected in almost all food samples, but different levels of interference were detected in different food matrices. Interpretation & conclusions: There is no immune detection system available commercially in India to detect botulism. The developed system might be useful for the detection of botulinum toxin in food and clinical samples. Further work is in progress.

Diseases triggered by microorganisms can be controlled by vaccines, which need neutralizing antigens. Hence, it is very crucial to identify extremely efficient immunogens for immune prevention. Botulism, a fatal neuroparalytic disease, is caused by botulinum neurotoxins produced by the anaerobic, Gram-positive spore-forming bacteria, Clostridium botulinum. Food-borne botulism and iatrogenic botulism are caused by botulinum toxin. Wound botulism, infant botulism, and adult intestinal botulism are caused by primarily C. botulinum followed by secondary intoxication. To identify protective antigens, whole cell proteome of C. botulinum type B was separated by two-dimensional gel electrophoresis. 2-D gel of whole cell proteins was probed with hyper immune sera of whole cell proteins of C. botulinum types A, E, and F. Six cross immunoreactive proteins were identified. These immunoreactive proteins will be further tested for developing vaccines and serodiagnostic markers against botulism.

Francisella tularensis , the causative agent of tularemia, has attained the status of one of the high priority agents that could be used in the act of bioterrorism. Currently, there is no licensed vaccine for this highly infectious intracellular pathogen. Being a listed ‘Category A’ agent of the U.S. Center for Disease Control and Prevention (CDC), vaccines and therapeutics are immediately required against this pathogen. In this study, an immunoproteomic approach based on the techniques of 2-dimensional gel electrophoresis (2DE) and immunoblotting combined with mass spectrometry (MS) was used for elucidation of immunogenic components and putative vaccine candidates. Whole-cell soluble protein extract of F. tularensis LVS (Ft LVS) was separated by 2DE, and immunoblots were developed with sera raised in rabbit after immunization with heat-killed Ft LVS. A total of 28 immunoreactive proteins were identified by tandem mass spectrometry. Rabbit immunoproteome of F. tularensis was compared with those previously reported using sera from human patients and in murine model. Out of 28 immunoreactive proteins identified in this study, 12 and 17 overlapping proteins were recognized by human and murine sera, respectively. Nine proteins were found immunogenic in all the three hosts, while eight new immunogenic proteins were found in this study. Identified immunoreactive proteins may find application in design and development of protein subunit vaccine for tularemia.

A total of 8 out of 11 deep ground water samples collected from different villages in Central India were found contaminated with Vibrio cholerae non O1, non O139. In a multiplex PCR, isolates were found positive for ompW gene but negative for ctxAB and rfbO1 genes . However, isolates from two places were positive for tcp and zot genes, indicating their intestinal colonization and toxigenic potential. Antibiotic susceptibility studies revealed that all isolates were multidrug resistant. Although, none of the isolates was found PCR positive for the mobile genetic elements, class 1 integrons and SXT constins. The results of this study corroborated that deep ground water can also be an important reservoir of V. cholerae in plane endemic areas, suggesting a continuous monitoring of water samples for timely prevention of the disease.