Institute of Microbial Technology

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Institute of Microbial Technology
Short name
IMTECH
Country, city
India, Chandigarh
Publications
2 538
Citations
88 092
h-index
125
Top-3 journals
Top-3 organizations

Most cited in 5 years

Klionsky D.J., Abdel-Aziz A.K., Abdelfatah S., Abdellatif M., Abdoli A., Abel S., Abeliovich H., Abildgaard M.H., Abudu Y.P., Acevedo-Arozena A., Adamopoulos I.E., Adeli K., Adolph T.E., Adornetto A., Aflaki E., et. al.
Autophagy scimago Q1 wos Q1 Open Access
2021-01-02 citations by CoLab: 1827 Abstract  
ABSTRACT In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.
Johnson R., Vishwakarma K., Hossen M.S., Kumar V., Shackira A.M., Puthur J.T., Abdi G., Sarraf M., Hasanuzzaman M.
2022-02-01 citations by CoLab: 235 Abstract  
Potassium (K) is an essential element for the growth and development of plants; however, its scarcity or excessive level leads to distortion of numerous functions in plants. It takes part in the control of various significant functions in plant advancement. Because of the importance index, K is regarded second after nitrogen for whole plant growth. Approximately, higher than 60 enzymes are reliant on K for activation within the plant system, in which K plays a vital function as a regulator. Potassium provides assistance in plants against abiotic stress conditions in the environment. With this background, the present paper reviews the physiological functions of K in plants like stomatal regulation, photosynthesis and water uptake. The article also focuses upon the uptake and transport mechanisms of K along with its role in detoxification of reactive oxygen species and in conferring tolerance to plants against abiotic stresses. It also highlights the research progress made in the direction of K mediated signaling cascades.
Vishwakarma K., Kumar N., Shandilya C., Mohapatra S., Bhayana S., Varma A.
Frontiers in Microbiology scimago Q1 wos Q2 Open Access
2020-12-21 citations by CoLab: 179 PDF Abstract  
The present scenario of agricultural sector is dependent hugely on the use of chemical-based fertilizers and pesticides that impact the nutritional quality, health status, and productivity of the crops. Moreover, continuous release of these chemical inputs causes toxic compounds such as metals to accumulate in the soil and move to the plants with prolonged exposure, which ultimately impact the human health. Hence, it becomes necessary to bring out the alternatives to chemical pesticides/fertilizers for improvement of agricultural outputs. The rhizosphere of plant is an important niche with abundant microorganisms residing in it. They possess the properties of plant growth promotion, disease suppression, removal of toxic compounds, and assimilating nutrients to plants. Utilizing such beneficial microbes for crop productivity presents an efficient way to modulate the crop yield and productivity by maintaining healthy status and quality of the plants through bioformulations. To understand these microbial formulation compositions, it becomes essential to understand the processes going on in the rhizosphere as well as their concrete identification for better utilization of the microbial diversity such as plant growth–promoting bacteria and arbuscular mycorrhizal fungi. Hence, with this background, the present review article highlights the plant microbiome aboveground and belowground, importance of microbial inoculants in various plant species, and their subsequent interactive mechanisms for sustainable agriculture.
Ali E.S., Sharker S.M., Islam M.T., Khan I.N., Shaw S., Rahman M.A., Uddin S.J., Shill M.C., Rehman S., Das N., Ahmad S., Shilpi J.A., Tripathi S., Mishra S.K., Mubarak M.S.
Seminars in Cancer Biology scimago Q1 wos Q1
2021-02-01 citations by CoLab: 167 Abstract  
Nanotechnology is reshaping health care strategies and is expected to exert a tremendous impact in the coming years offering better healthcare facilities. It has led to not only therapeutic drug delivery feasibility but also to diagnostics. Materials in the size of nano range (1-100 nm) used in the design, fabrication, regulation, and application of therapeutic drugs or devices are classified as medical nanotechnology and nanopharmacology. Delivery of more complex molecules to the specific site of action as well as gene therapy has pushed forward the nanoparticle-based drug delivery to its maximum. Areas that benefit from nano-based drug delivery systems are cancer, diabetes, infectious diseases, neurodegenerative diseases, blood disorders and orthopedic-related ailments. Moreover, development of nanotherapeutics with multi-functionalities has a considerable potential to fill the gaps that exist in the present therapeutic domain. In cancer treatment, nanomedicines have superiority over current therapeutic practices as they can effectively deliver the drug to the affected tissues, thus reducing drug toxicities. Along this line, polymeric conjugates of asparaginase and polymeric micelles of paclitaxel have recently been recommended for the treatment of various types of cancers. Nanotechnology-based therapeutics and diagnostics provide greater effectiveness with less or no toxicity concerns. Similarly, diagnostic imaging holds promising future applications with newer nano-level imaging elements. Advancements in nanotechnology have emerged to a newer direction which use nanorobotics for various applications in healthcare. Accordingly, this review comprehensively highlights the potentialities of various nanocarriers and nanomedicines for multifaceted applications in diagnostics and drug delivery, especially the potentialities of polymeric nanoparticle, nanoemulsion, solid-lipid nanoparticle, nanostructured lipid carrier, self-micellizing anticancer lipids, dendrimer, nanocapsule and nanosponge-based therapeutic approaches in the field of cancer. Furthermore, this article summarizes the most recent literature pertaining to the use of nano-technology in the field of medicine, particularly in treating cancer patients.
Chakraborty P., Bajeli S., Kaushal D., Radotra B.D., Kumar A.
Nature Communications scimago Q1 wos Q1 Open Access
2021-03-11 citations by CoLab: 150 PDF Abstract  
Tuberculosis is a chronic disease that displays several features commonly associated with biofilm-associated infections: immune system evasion, antibiotic treatment failures, and recurrence of infection. However, although Mycobacterium tuberculosis (Mtb) can form cellulose-containing biofilms in vitro, it remains unclear whether biofilms are formed during infection in vivo. Here, we demonstrate the formation of Mtb biofilms in animal models of infection and in patients, and that biofilm formation can contribute to drug tolerance. First, we show that cellulose is also a structural component of the extracellular matrix of in vitro biofilms of fast and slow-growing nontuberculous mycobacteria. Then, we use cellulose as a biomarker to detect Mtb biofilms in the lungs of experimentally infected mice and non-human primates, as well as in lung tissue sections obtained from patients with tuberculosis. Mtb strains defective in biofilm formation are attenuated for survival in mice, suggesting that biofilms protect bacilli from the host immune system. Furthermore, the administration of nebulized cellulase enhances the antimycobacterial activity of isoniazid and rifampicin in infected mice, supporting a role for biofilms in phenotypic drug tolerance. Our findings thus indicate that Mtb biofilms are relevant to human tuberculosis. Mycobacterium tuberculosis forms biofilms in vitro, but it is unclear whether biofilms are also formed during infection in vivo. Here, Chakraborty et al. demonstrate the formation of biofilms in animal models of infection and in patients with tuberculosis, and that biofilm formation can contribute to drug tolerance.
Sarraf M., Vishwakarma K., Kumar V., Arif N., Das S., Johnson R., Janeeshma E., Puthur J.T., Aliniaeifard S., Chauhan D.K., Fujita M., Hasanuzzaman M.
Plants scimago Q1 wos Q1 Open Access
2022-01-25 citations by CoLab: 132 PDF Abstract  
In agriculture, abiotic stress is one of the critical issues impacting the crop productivity and yield. Such stress factors lead to the generation of reactive oxygen species, membrane damage, and other plant metabolic activities. To neutralize the harmful effects of abiotic stress, several strategies have been employed that include the utilization of nanomaterials. Nanomaterials are now gaining attention worldwide to protect plant growth against abiotic stresses such as drought, salinity, heavy metals, extreme temperatures, flooding, etc. However, their behavior is significantly impacted by the dose in which they are being used in agriculture. Furthermore, the action of nanomaterials in plants under various stresses still require understanding. Hence, with this background, the present review envisages to highlight beneficial role of nanomaterials in plants, their mode of action, and their mechanism in overcoming various abiotic stresses. It also emphasizes upon antioxidant activities of different nanomaterials and their dose-dependent variability in plants’ growth under stress. Nevertheless, limitations of using nanomaterials in agriculture are also presented in this review.
McCormick E.M., Lott M.T., Dulik M.C., Shen L., Attimonelli M., Vitale O., Karaa A., Bai R., Pineda‐Alvarez D.E., Singh L.N., Stanley C.M., Wong S., Bhardwaj A., Merkurjev D., Mao R., et. al.
Human Mutation scimago Q1 wos Q2
2020-11-10 citations by CoLab: 109 Abstract  
Mitochondrial DNA (mtDNA) variant pathogenicity interpretation has special considerations given unique features of the mtDNA genome, including maternal inheritance, variant heteroplasmy, threshold effect, absence of splicing, and contextual effects of haplogroups. Currently, there are insufficient standardized criteria for mtDNA variant assessment, which leads to inconsistencies in clinical variant pathogenicity reporting. An international working group of mtDNA experts was assembled within the Mitochondrial Disease Sequence Data Resource Consortium and obtained Expert Panel status from ClinGen. This group reviewed the 2015 American College of Medical Genetics and Association of Molecular Pathology standards and guidelines that are widely used for clinical interpretation of DNA sequence variants and provided further specifications for additional and specific guidance related to mtDNA variant classification. These Expert Panel consensus specifications allow for consistent consideration of the unique aspects of the mtDNA genome that directly influence variant assessment, including addressing mtDNA genome composition and structure, haplogroups and phylogeny, maternal inheritance, heteroplasmy, and functional analyses unique to mtDNA, as well as specifications for utilization of mtDNA genomic databases and computational algorithms.
Sharma R., Mishra A., Pant D., Malaviya P.
Bioresource Technology scimago Q1 wos Q1
2022-01-01 citations by CoLab: 91 Abstract  
The ability of microalgae to grow in a broad spectrum of wastewaters manifests great potentials for removing contaminants from effluents of industries and urban areas. Since the post-treatment microalgae biomass is also a significant source of high-value products, microalgae-based wastewater treatment is an economical and sustainable solution to wastewater management. Adding more value, the integration of microalgae with living/non-living materials looks more promising. Microalgae-based treatment technology has certain limitations like high operational costs, problematic harvesting, large land requirements, and hindrance in photosynthesis due to turbid wastewater. These challenges need to be essentially addressed to achieve enhanced wastewater remediation. This review has highlighted the potential applications of microalgae in contaminant removal from wastewaters, simultaneous resource recovery, efficient microalgae-based hybrid systems along with bottlenecks and prospects. This state-of-the-art article will edify the role of microalgae in wastewater remediation, biomass valorization for bio-based products, and present numerous possibilities in strengthening the circular bioeconomy.
Gupta R., Kumar A., Kumar S., Pinnaka A.K., Singhal N.K.
2021-02-01 citations by CoLab: 88 Abstract  
• Successfully generated aptamers against E. coli bacterial cells through Cell-SELEX. • Aptamer-nanoprobe based sensitive and selective visual detection assay for E. coli was developed. • Graphene oxide enhances the loading capacity of aptamer on nanoprobe making it more sensitive. • Limit of detection using this nanoprobe was 10 2 cells/mL in Mili Q water and spiked coconut water. • The proposed detection assay was performed in glass capillary to mimic microfluidic channel. E. coli is the most common foodborne bacteria causing illnesses including diarrhea, fever, and death if left undiagnosed and untreated, which makes its detection most important. Traditional detection methods such as culture methods, PCR, or ELISA are time-consuming and require skilled manpower. To overcome the disadvantages of traditional detection methods, a fast, easy, and cost-effective platform is required. ssDNA aptamer is a stable, sensitive, and selective biomolecule used extensively for detection. To provide naked eye visible detection, gold nanoparticles (AuNPs) were used, and to increase the aptamer conjugation, AuNPs were covered with Graphene Oxide. Thus, the overall sensitivity of the designed nanoprobe was also augmented. Therefore, exploiting the properties of gold nanoparticles and graphene oxide, a detection platform with aptamer conjugation has been developed in this study. In the manifestation of E. coli cells, the visible color change was observed from red to blue within an hour incubation. The limit of detection observed visually was 10 2 cells/mL with GO coating and 10 3 cells/mL without GO. The detection limit in real time coconut water samples was also 10 2 cells/mL. This platform was found to be applicable in glass capillary which provides opportunities for making a point of care detection device.
Tripathi D.K., Vishwakarma K., Singh V.P., Prakash V., Sharma S., Muneer S., Nikolic M., Deshmukh R., Vaculík M., Corpas F.J.
Journal of Hazardous Materials scimago Q1 wos Q1
2021-04-01 citations by CoLab: 88 Abstract  
Exogenous applications of silicon (Si) can initiate cellular defence pathways to enhance plant resistance to abiotic and biotic stresses. Plant Si accumulation is regulated by several transporters of silicic acid (e.g. Lsi1, Lsi2, and Lsi6), but the precise mechanisms involved in overall Si transport and its beneficial effects remains unclear. In stressed plants, the accumulation of Si leads to a defence mechanism involving the formation of amorphous or hydrated silicic acid caused by their polymerization and interaction with other organic substances. Silicon also regulates plant ionic homeostasis, which involves the nutrient acquisition, availability, and replenishment in the soil through biogeochemical cycles. Furthermore, Si is implicated in modulating ethylene-dependent and jasmonate pathways, as well as other phytohormones, particularly under stress conditions. Crosstalk between Si and phytohormones could lead to improvements in Si-mediated crop growth, especially when plants are exposed to stress. The integration of Si with reactive oxygen species (ROS) metabolism appears to be a part of the signaling cascade that regulates plant phytohormone homeostasis, as well as morphological, biochemical, and molecular responses. This review aims to provide an update on Si interplays with ROS, phytohormones, and other signaling molecules that regulate plant development under stress conditions. • Silicon is beneficial for the plants. • Silicon (Si) can mediate plant growth and development under stress conditions. • Si interplays with reactive oxygen species of plants under stress. • Signaling molecules underpins the beneficial impact of silicon in plants.
Joshi A., Thite S., Godbole D., Boruah D., Sindhu D.K., Prabhu A., Joseph N., Yadav A., Sharma A., Lodha T.
Antonie van Leeuwenhoek scimago Q2 wos Q4
2025-02-10 citations by CoLab: 0 Abstract  
Two Gram-stain-negative bacterial strains (MEB164T and MEB148), were isolated from haloalkaline waters of Lonar, crater lake, India. The strains were helical, non-spore-forming and motile with polar tufts of flagella. Optimal growth occurred at 37 ℃, at pH 10 and with 3% (w/v) NaCl. 16S rRNA gene sequences of strains (MEB164T and MEB148) demonstrated the highest similarity with Marinospirillum alkaliphilum DSM 21637T (97.8%) followed by Marinospirillum celere DSM 18438T (96%). The genome size of strain MEB164T was determined to be 2.8 Mb with genomic DNA G + C contents of 53.1 mol %. ANI and dDDH values between strain MEB164T and the most closely related type strain M. alkaliphilum DSM 21637T were (72.3% and 21.4 ± 2.3%) while (AAI and POCP) values were (66.8 and 70.8%), respectively. Strain MEB164T exhibited potential for polyhydroxybutyrate (PHB) production, supported by key genes involved in PHB metabolism. Genome analysis further revealed presence of various pH tolerance genes, highlighting its adaptation to Lonar Lake. The predominant cellular fatty acids were summed feature 8 (C18:1 ω7c/C18:1 ω6c), C16:0 and summed feature 3 (C16:1 ω7c/C16:1 ω6c). The major respiratory quinone was ubiquinone-8. The prevalent polar lipids were diaminophosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, two unidentified amino phospholipids, three unidentified phospholipids and one unidentified lipid. Polyphasic analysis suggests that the two strains constitute a novel species within the genus Marinospirillum (family Oceanospirillaceae), proposed as Marinospirillum alkalitolerans sp. nov. The type strain is MEB164T (= JCM 35957T = MCC 5207T = NCIMB 15458T) and MEB148 (= JCM 35956 = MCC 5212 = NCIMB 15459) is an additional strain.
Srivastava S., Rana V.S., Singh R.
Current Microbiology scimago Q2 wos Q3
2025-02-07 citations by CoLab: 0 Abstract  
Antibiotic resistance poses the biggest threats to global health and development and also to food security. β-lactam antibiotics (BLAs) responsible for the transpeptidation/cross-linking process during cell wall biosynthesis contribute to the maximum resistance. The production of β-lactamase enzyme is a significant contributing factor to the development of antibiotic resistance to β-lactam antibiotics. Unintentional disposal of antibiotics from the manufacturing units of pharma industries to the water bodies enhances the exposure of antibiotics, contributing to resistance. This study describes the presence of > 50 antibiotic-resistant bacterial strains in pharma effluent of Himachal Pradesh, India. Among 54 isolates, 40% showed ampicillin resistance above 100 µg/mL, 13% showed resistance above 5000 µg/mL, and 3 strains showed resistance at 15,000 µg/mL of ampicillin. Enterobacter hormaechei RSM5 showed the highest minimum inhibitory concentration (MIC) and cell viability and was selected for further studies. It produces lactamase (0.24 U/mL) to resist the higher concentration of antibiotics present in the media/effluent and demonstrated resistance against 3 different classes of antibiotics, confirming its status as a multidrug resistance (MDR) strain. The high-performance liquid chromatography (HPLC) analysis of the isolate demonstrated that Enterobacter hormaechei RSM5 can degrade ampicillin within 24 h of incubation in medium/effluent. The emergence of Enterobacter as a pathogen with antibiotic resistance poses a significant health concern that could also be explored for the removal of antibiotics from the effluent at the source. The future of research in this area needs to be open and mindful of new approaches.
Kundu N., Yadav S., Bhattacharya A., Aseri G.K., Jain N.
Letters in Applied Microbiology scimago Q3 wos Q4
2025-01-25 citations by CoLab: 0 Abstract  
Abstract Azo dyes constitute 60–70% of commercially used dyes and are complex, carcinogenic, and mutagenic pollutants that negatively impact soil composition, water bodies, flora, and fauna. Conventional azo dye degradation techniques have drawbacks such as high production and maintenance costs, use of hazardous chemicals, membrane clogging, and sludge generation. Constructed Wetland—Microbial Fuel Cells (CW-MFCs) offer a promising sustainable approach for the bio-electrodegradation of azo dyes from textile wastewater. CW-MFCs harness the phytodegradation capabilities of wetland plants like Azolla, water hyacinth, and Ipomoea, along with microalgae such as Nostoc, Oscillatoria, Chlorella, and Anabaena, to break down azo dyes into aromatic amines. These intermediates are then reduced to CO2 and H2O by microalgae in the fuel cells, while simultaneously generating electricity. CW-MFCs offer advantages including low cost, sustainability, and use of renewable energy. The valorization of the resulting algal and plant biomass further enhances the sustainability of this approach, as it can be used for biofuel production, nutraceuticals, pharmaceuticals, and bio-composting. Implementing CW-MFCs as a tertiary treatment step in textile industries aligns with the circular economy concept and contributes to achieving several Sustainable Development Goals (SDGs).
Liu Y., Geng Y., Jiang Y., Li P., Li Y., Zhang Z.
ISME Journal scimago Q1 wos Q1
2025-01-24 citations by CoLab: 1 Abstract  
Abstract One of the central questions in microbial ecology is how to explain the high biodiversity of communities. A large number of rare taxa in the community have not been excluded by abundant taxa with competitive advantages, a contradiction known as the biodiversity paradox. Recently, increasing evidence has revealed the central importance of antimicrobial toxins as crucial weapons of antagonism in microbial survival. The powerful effects of antimicrobial toxins result in simple combinations of microorganisms failing to coexist under laboratory conditions, but it is unclear whether they also have a negative impact on the biodiversity of natural communities. Here, we revealed that microbial communities worldwide universally possess functional potential for antimicrobial toxin production. Counterintuitively, the biodiversity of global microbial communities increases, rather than decreases, as the abundance of antimicrobial toxins in rare taxa rises. Rare taxa may encode more antimicrobial toxins than abundant taxa, which is associated with the maintenance of the high biodiversity of microbial communities amid complex interactions. Our findings suggest that the antagonistic interaction caused by antimicrobial toxins may play a positive role in microbial community biodiversity at the global scale.
Bhardwaj P., Bisht B., Bhalla V.
Nanoscale scimago Q1 wos Q1
2025-01-23 citations by CoLab: 0 Abstract  
Interaction of urease with four different sizes (5–100 nm) of silver nanoparticles and inhibition studies.
Priya M., Gupta S.K., Koundal A., Kapoor S., Tiwari S., Kidwai S., Sorio de Carvalho L.P., Thakur K.G., Mahajan D., Sharma D., Kumar Y., Singh R.
2025-01-22 citations by CoLab: 0 Abstract  
Itaconate, an abundant metabolite produced by macrophages upon interferon-γ stimulation, possesses both antibacterial and immunomodulatory properties. Despite its crucial role in immunity and antimicrobial control, its mechanism of action and dissimilation are poorly understood. Here, we demonstrate that infection of mice with Mycobacterium tuberculosis increases itaconate levels in lung tissues. We also show that exposure to itaconate inhibits M. tuberculosis growth in vitro, in macrophages, and mice. We report that exposure to sodium itaconate (ITA) interferes with the central carbon metabolism of M. tuberculosis . In addition to the inhibition of isocitrate lyase (ICL), we demonstrate that itaconate inhibits aldolase and inosine monophosphate (IMP) dehydrogenase in a concentration-dependent manner. Previous studies have shown that Rv2498c from M. tuberculosis is the bona fide (S)-citramalyl-CoA lyase, but the remaining components of the pathway remain elusive. Here, we report that Rv2503c and Rv3272 possess itaconate:succinyl-CoA transferase activity, and Rv2499c and Rv3389c possess itaconyl-CoA hydratase activity. Relative to the parental and complemented strains, the ΔRv3389c strain of M. tuberculosis was attenuated for growth in itaconate-containing medium, in macrophages, mice, and guinea pigs. The attenuated phenotype of ΔRv3389c strain of M. tuberculosis is associated with a defect in the itaconate dissimilation and propionyl-CoA detoxification pathway. This study thus reveals that multiple metabolic enzymes are targeted by itaconate in M. tuberculosis. Furthermore, we have assigned the two remaining enzymes responsible for the degradation of itaconic acid into pyruvate and acetyl-CoA. Finally, we also demonstrate the importance of enzymes involved in the itaconate dissimilation pathway for M. tuberculosis pathogenesis.
Saran A., Agarwal A., Mali S.A., Singhal L., Patil P.B., Gautam V.
2025-01-18 citations by CoLab: 0 Abstract  
Burkholderia cepacia complex (Bcc) is an opportunistic pathogen that causes severe infections in immunocompromised individuals. It is a common contaminant of medical drugs, solutions and devices used in healthcare setups. This scoping review aimed to assess Bcc outbreaks in Indian hospital settings and address a wide range of sources to improve outbreak management. As per PRISMA-ScR guidelines, electronic databases ‘Embase’, ‘PubMed’ and ‘Web of Science’ were searched from 1993 to September 2024 to identify studies reporting Burkholderia cepacia complex outbreaks across India. The search identified 22 outbreak reports meeting the inclusion criteria. Bacteremia was the most common presentation in twenty studies, followed by acute-onset post-operative endophthalmitis in two studies. In 14 outbreak studies, B. cepacia was the identified species, whereas five studies had Bcc; one study each had B. cenocepacia, B. multivorans and B. contaminans isolated. Most outbreaks were associated with contaminated pharmaceuticals (45.4%) and medical (18.1%) products in contrast to the environment as a source (13.6%). Multi-locus sequence typing (MLST) was employed to study clonality among isolates in six outbreaks. This review highlights that varied medical products and environmental surfaces/objects can harbour Bcc and act as potential sources of Bcc outbreaks in hospitals. Ensuring immediate identification of Bcc from clinical samples, regular sterility checks, thorough epidemiological investigations, and timely infection control and prevention measures are critical to help manage and prevent these outbreaks and the subsequent mortality.
Singh S., Arya G., Mishra R., Singla S., Pratap A., Upadhayay K., Sharma M., Chaba R.
Nucleic Acids Research scimago Q1 wos Q1 Open Access
2025-01-07 citations by CoLab: 0 PDF Abstract  
Abstract GntR/FadR family featuring an N-terminal winged helix–turn–helix DNA-binding domain and a C-terminal α-helical effector-binding and oligomerization domain constitutes one of the largest families of transcriptional regulators. Several GntR/FadR regulators govern the metabolism of sugar acids, carbon sources implicated in bacterial–host interactions. Although effectors are known for a few sugar acid regulators, the unavailability of relevant structures has left their allosteric mechanism unexplored. Here, using DgoR, a transcriptional repressor of d-galactonate metabolism in Escherichia coli, as a model, and its superrepressor alleles, we probed allostery in a GntR/FadR family sugar acid regulator. Genetic and biochemical studies established compromised response to d-galactonate as the reason for the superrepressor behavior of the mutants: T180I does not bind d-galactonate, and while A97V, S171L and M188I bind d-galactonate, effector binding does not induce a conformational change required for derepression, suggesting altered allostery. For mechanistic insights into allosteric communication, we performed simulations of the modeled DgoR structure in different allosteric states for both the wild-type and mutant proteins. We found that each mutant exhibits unique dynamics disrupting the intrinsic allosteric communication pathways, thereby impacting DgoR function. We finally validated the allosteric communication model by testing in silico predictions with experimental data.
Kundu D., Martoliya Y., Sharma A., Partap Sasan S., Wasi M., Prasad R., Mondal A.K.
Gene scimago Q2 wos Q2
2025-01-01 citations by CoLab: 1 Abstract  
Group III hybrid histidine kinases (HHK3) are known molecular targets of the widely used fungicidal agent fludioxonil which indirectly converts these kinases to a phosphatase form that causes constitutive activation of Hog1 MAPK. To better understand the fungicidal effect of fludioxonil we have screened S. cerevisiae haploid deletion collection for fludioxonil resistant mutant and identified Ssd1 as a critical factor for this. Deletion of SSD1 not only promoted resistance to fludioxonil but also abrogated Hog1 activation and other cellular damages caused by fludioxonil. Our results showed that fludioxonil perturbed the localization of Cbk1 kinase, an essential protein in yeast, at the bud neck triggering the accumulation of Ssd1 in P-bodies. As a result, localized synthesis of Ssd1 bound mRNA encoding cell wall proteins at the polarized growth site was impaired which created a sustained cell wall stress causing constitutive activation of Hog1. Our data, for the first time, clearly indicated the role of Cbk1 upstream of Hog1 and provided a novel paradigm in the mechanism of action of fludioxonil.
Ahmed M., Kurungottu P., Swetha K., Atla S., Ashok N., Nagamalleswari E., Bonam S.R., Sahu B.D., Kurapati R.
Biomaterials Science scimago Q1 wos Q1
2025-01-01 citations by CoLab: 1 Abstract  
The nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family pyrin domain-containing 3 (NLRP3) inflammasome is pivotal in orchestrating the immune response induced by most of the nanoparticle adjuvants.
Sharma Y., Kaur S., Kandhasamy H., Sahoo S.C., Chaudhari V.D.
Organic Letters scimago Q1 wos Q1
2024-12-31 citations by CoLab: 0
Srivastava P., Subramanian S., Manickam N.
Journal of Applied Microbiology scimago Q2 wos Q2
2024-12-20 citations by CoLab: 0 Abstract  
Abstract Aims To isolate polyethylene terephthalate (PET)-degrading bacteria and elucidate the underlying mechanisms of PET biodegradation through biochemical and genome analysis. Methods and results Rhodococcus rhodochrous IITR131 was found to degrade PET. Strain IITR131 genome revealed metabolic versatility of the bacterium and had the ability to form biofilm on PET sheet, resulting in the cracks, abrasions, and degradation. IITR131 showed a reduction of 19.7%, exhibiting a half-life of 189.9 d of 0.1 mm PET film in 60 d and formed metabolites bis(2-hydroxyethyl) terephthalate (BHET), terephthalic acid (TPA), and benzoic acid (BA). The draft genome of 5.9 Mb of IITR131 revealed that this bacterium has plethora of genes such as terephthalate 1, 2 dioxygenase, carboxylesterase that together constituted a complete pathway for PET degradation. Moreover, strain IITR131 was found to have a variety of genes encoding for enzymes for the metabolism of several plastic polymers, xenobiotics including chloroalkanes, and polycyclic aromatic hydrocarbons. Conclusions Rhodococcus rhodochrous IITR131 demonstrated a significant potential in the biodegradation of PET. The comprehensive genomic and metabolic analyses further elucidated the molecular pathway involved in PET degradation, enhancing our understanding of the mechanisms underlying microbial PET biodegradation. These findings underscore the applicability of R. rhodochrous IITR131 in biotechnological approaches for mitigating plastic pollution.
Kamboj S., Kumar M.
Journal of Medical Virology scimago Q1 wos Q1
2024-12-19 citations by CoLab: 1 Abstract  
ABSTRACTHepatitis C virus (HCV) is a pathogenic virus of global health concern. The phylodynamics of HCV genotypes/subtypes 1a, 1b, 2, and 3 are explored only for specific geographic regions. However, their genome based global origin and detailed spatiotemporal spread, have yet to be extensively studied. To study the global evolution of “epidemic” HCV genotypes/subtypes, we screened all available HCV complete genome sequences (n = 2744) from 27 countries worldwide for over four decades. We used representative sequences (n = 516) for phylodynamic and phylogeographic analyses, examining HCV worldwide origin, transmission, and spatiotemporal spread. We are the first to study the global phylogeography of genotype 2. The evolutionary rates for genotype/subtype 1a, 1b, 2, and 3 are 1.109 × 10‐3, 1.096 × 10‐3, 5.013 × 10‐3 and 1.483 × 10‐3 substitutions/site/year respectively. We deduced tMRCAs and origin location of respective HCV genotype/subtype as 1909.21 (United States), 1893.36 (Japan), 981.76 (France), and 1714.89 (India). We estimated their migration pattern with time to and from different continents. The origin location of genotype 2 was estimated to be France instead of previous postulated African origin. This can be related to slave trade, French colonization, and previous studies on specific geographic regions only. HCV genotypes/subtypes showed transmission and expansion due to factors like World War II, iatrogenic infections, “baby boomer” population, inefficient medical screening, intravenous drug use, decline due to antiviral therapy introduction. Our study provides novel and extensive information about the evolutionary history and spatiotemporal spread of the HCV genotypes responsible for most infections worldwide.
Choudhury J., Chaudhuri B.N.
Cytoskeleton scimago Q2 wos Q4
2024-12-19 citations by CoLab: 0 Abstract  
ABSTRACTZ‐ring formation by FtsZ, the master assembler of the divisome, is a key step in bacterial cell division. Membrane anchoring of the Z‐ring requires the assistance of dedicated Z‐ring binding proteins, such as SepF and FtsA. SepF participates in bundling and membrane anchoring of FtsZ in gram‐positive bacteria. We report in vitro biophysical studies of the interactions between FtsZ and a cytoplasmic component of cognate SepF from three different bacteria: Mycobacterium tuberculosis, Staphylococcus aureus, and Enterococcus gallinarum. While the cytosolic domain of SepF from M. tuberculosis is primarily a dimer, those from S. aureus and E. gallinarum polymerize to form ring‐like structures. Mycobacterial SepF helps in the bundling of FtsZ filaments to form thick filaments and large spirals. On the other hand, ring‐forming SepF from the Firmicutes bundle FtsZ into tubules. Our results suggest that the oligomeric form of SepF directs how it bundles FtsZ filaments.

Since 1985

Total publications
2538
Total citations
88092
Citations per publication
34.71
Average publications per year
63.45
Average authors per publication
7.5
h-index
125
Metrics description

Top-30

Fields of science

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General Medicine, 610, 24.03%
Biochemistry, 555, 21.87%
Molecular Biology, 553, 21.79%
Microbiology, 451, 17.77%
Biotechnology, 340, 13.4%
Applied Microbiology and Biotechnology, 301, 11.86%
Genetics, 259, 10.2%
Cell Biology, 226, 8.9%
Bioengineering, 213, 8.39%
Multidisciplinary, 187, 7.37%
Ecology, Evolution, Behavior and Systematics, 172, 6.78%
Microbiology (medical), 151, 5.95%
Structural Biology, 141, 5.56%
Biophysics, 123, 4.85%
Immunology, 120, 4.73%
Infectious Diseases, 115, 4.53%
General Chemistry, 88, 3.47%
Plant Science, 87, 3.43%
Pharmacology, 82, 3.23%
General Biochemistry, Genetics and Molecular Biology, 79, 3.11%
Immunology and Allergy, 79, 3.11%
Organic Chemistry, 76, 2.99%
Molecular Medicine, 67, 2.64%
Analytical Chemistry, 58, 2.29%
General Chemical Engineering, 57, 2.25%
Computer Science Applications, 55, 2.17%
General Agricultural and Biological Sciences, 55, 2.17%
Biomedical Engineering, 51, 2.01%
Agronomy and Crop Science, 51, 2.01%
Drug Discovery, 49, 1.93%
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With foreign organizations

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With other countries

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USA, 213, 8.39%
Germany, 72, 2.84%
Australia, 42, 1.65%
United Kingdom, 40, 1.58%
China, 39, 1.54%
Japan, 33, 1.3%
France, 27, 1.06%
Republic of Korea, 27, 1.06%
Saudi Arabia, 24, 0.95%
Canada, 22, 0.87%
Brazil, 17, 0.67%
Bangladesh, 16, 0.63%
Singapore, 15, 0.59%
Italy, 14, 0.55%
Sweden, 14, 0.55%
Switzerland, 13, 0.51%
Iran, 12, 0.47%
Spain, 11, 0.43%
Netherlands, 11, 0.43%
Nepal, 10, 0.39%
Russia, 9, 0.35%
Portugal, 9, 0.35%
South Africa, 9, 0.35%
Israel, 8, 0.32%
Denmark, 7, 0.28%
Tunisia, 7, 0.28%
Czech Republic, 7, 0.28%
Austria, 6, 0.24%
Hungary, 6, 0.24%
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  • We do not take into account publications without a DOI.
  • Statistics recalculated daily.
  • Publications published earlier than 1985 are ignored in the statistics.
  • The horizontal charts show the 30 top positions.
  • Journals quartiles values are relevant at the moment.