Salmonella, a foodborne pathogen, poses a significant threat to public health. This concern is exacerbated by emerging antibiotic resistance. Bacteriophages and their endolysins are promising alternatives to antibiotics. Endolysins play a crucial role in bacterial lysis in the phage life cycle. Leveraging these proteins as antimicrobial agents may offer a potential solution for controlling pathogenic contamination in food. Structural and functional analysis of LysSM5 endolysin derived from vB_SenA_SM5, a Salmonella phage, was studied using computational tools. Functional annotation, physicochemical characteristics, and 3D structure of the LysSM5 were predicted. Validation and quality assessment were performed using various computational tools like Conserved Domain Search, ProtParam, SWISS-Model server, PROCHECK, Verify3D, and ERRAT server. The molecular weight of LysSM5 was 28.8 kDa, 264 amino acids, and an isoelectric point of 8.9. The sequence of LysSM5 comprised of an N-terminal peptidoglycan-binding domain (residues 9-64) and a C-terminal N-acetyl-β-D-muramidase domain (residues 90-263), interconnected by a linker sequence. Phylogenetic analysis using MEGA X revealed that LysSM5 shared similarities with endolysins from phages active against E. coli and various Salmonella serovars. This indicates that LysSM5 may have a broad spectrum of activity, making it a versatile candidate for combating a range of bacterial pathogens. The structure was predicted by using the SWISS-Model server, validated by Ramachandran plot analysis (91.8% residues in favored regions) and quality assessments (ERRAT score: 98.016, Verify3D: 95.44% residues with ≥ 0.1 score). These high-quality scores confirm that LysSM5's predicted structure is accurate and reliable for further analysis. Molecular docking showed a robust binding affinity of LysSM5 to peptidoglycan (- 13.9 kcal/mol), indicating its potential effectiveness in targeting and interacting with bacterial cell walls for antimicrobial applications. Molecular dynamics simulations were performed using the iMODS web server, indicating high stability of the LysSM5-peptidoglycan complex, with an eigenvalue of 8.873650e-05, suggesting that LysSM5 can effectively bind to and disrupt bacterial cell walls, making it a promising candidate for further development in antimicrobial applications.
沙门氏菌是一种食源性病原体,对公众健康构成重大威胁。抗生素耐药性的出现加剧了这种担忧。噬菌体及其内溶素是很有前途的抗生素替代品。在噬菌体生命周期中,内溶素在细菌裂解中起着至关重要的作用。利用这些蛋白质作为抗菌剂可能为控制食品中的致病性污染提供一种潜在的解决方案。利用计算工具对沙门氏菌噬菌体vB_SenA_SM5衍生的LysSM5内溶素进行了结构和功能分析。对LysSM5的功能注释、理化特性和三维结构进行了预测。使用各种计算工具进行验证和质量评估,如保守域搜索、ProtParam、SWISS-Model服务器、PROCHECK、Verify3D和ERRAT服务器。LysSM5分子量28.8 kDa, 264个氨基酸,等电点8.9。LysSM5的序列由一个n端肽聚糖结合域(残基9-64)和一个c端n-乙酰-β- d -酶结构域(残基90-263)组成,它们通过一个连接子序列相互连接。利用MEGA X进行系统发育分析,发现LysSM5与大肠杆菌和多种沙门氏菌血清型噬菌体的内溶素具有相似性。这表明LysSM5可能具有广泛的活性,使其成为对抗一系列细菌病原体的多功能候选物。利用SWISS-Model server对结构进行预测,通过Ramachandran图分析(91.8%的残差在有利区域)和质量评估(ERRAT评分:98.016,Verify3D评分:95.44%的残差≥0.1)进行验证。这些高质量的分数证实了LysSM5预测的结构是准确可靠的,可以进行进一步的分析。分子对接显示LysSM5与肽聚糖的结合亲和力较强(- 13.9 kcal/mol),表明其在抗菌应用中靶向细菌细胞壁并与之相互作用的潜在有效性。利用iMODS web服务器进行分子动力学模拟,结果表明LysSM5肽聚糖复合物具有较高的稳定性,特征值为8.873650e-05,表明LysSM5可以有效地结合并破坏细菌细胞壁,具有进一步开发抗菌应用的潜力。
{"title":"Unveiling the Virtual Blueprint: Exploring the Structural and Functional Analysis of a Novel Endolysin LysSM5 Derived from Salmonella phage vB_SenA_SM5.","authors":"Kritika Sharma, Harpreet Kaur, Naveen Chaudhary, Surender Prajapati, Balvinder Mohan, Neelam Taneja","doi":"10.1007/s12088-024-01431-2","DOIUrl":"https://doi.org/10.1007/s12088-024-01431-2","url":null,"abstract":"<p><p><i>Salmonella</i>, a foodborne pathogen, poses a significant threat to public health. This concern is exacerbated by emerging antibiotic resistance. Bacteriophages and their endolysins are promising alternatives to antibiotics. Endolysins play a crucial role in bacterial lysis in the phage life cycle. Leveraging these proteins as antimicrobial agents may offer a potential solution for controlling pathogenic contamination in food. Structural and functional analysis of LysSM5 endolysin derived from vB_SenA_SM5, a <i>Salmonella</i> phage, was studied using computational tools. Functional annotation, physicochemical characteristics, and 3D structure of the LysSM5 were predicted. Validation and quality assessment were performed using various computational tools like Conserved Domain Search, ProtParam, SWISS-Model server, PROCHECK, Verify3D, and ERRAT server. The molecular weight of LysSM5 was 28.8 kDa, 264 amino acids, and an isoelectric point of 8.9. The sequence of LysSM5 comprised of an N-terminal peptidoglycan-binding domain (residues 9-64) and a C-terminal N-acetyl-β-D-muramidase domain (residues 90-263), interconnected by a linker sequence. Phylogenetic analysis using MEGA X revealed that LysSM5 shared similarities with endolysins from phages active against <i>E. coli</i> and various <i>Salmonella</i> serovars. This indicates that LysSM5 may have a broad spectrum of activity, making it a versatile candidate for combating a range of bacterial pathogens. The structure was predicted by using the SWISS-Model server, validated by Ramachandran plot analysis (91.8% residues in favored regions) and quality assessments (ERRAT score: 98.016, Verify3D: 95.44% residues with ≥ 0.1 score). These high-quality scores confirm that LysSM5's predicted structure is accurate and reliable for further analysis. Molecular docking showed a robust binding affinity of LysSM5 to peptidoglycan (- 13.9 kcal/mol), indicating its potential effectiveness in targeting and interacting with bacterial cell walls for antimicrobial applications. Molecular dynamics simulations were performed using the iMODS web server, indicating high stability of the LysSM5-peptidoglycan complex, with an eigenvalue of 8.873650e-05, suggesting that LysSM5 can effectively bind to and disrupt bacterial cell walls, making it a promising candidate for further development in antimicrobial applications.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"66 1","pages":"108-119"},"PeriodicalIF":1.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12909675/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146219619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Beginning with the centralization of young tea (Yt) to encourage low branch growth, subsequent light pruning (LP) and deep skiffing (DS) techniques are employed to promote branch spread, ensuring an ideal leaf area index and manageable plucking height. This study investigates the effects of LP and DS compared to Yt on soil biota, a previously unexplored topic. Soil samples from Yt, LP, and DS sites within the Rajgarh Tea Estate in Assam, India, were analyzed for standard parameters and metagenomic DNA using Illumina sequencing. While all samples exhibited a clay loam texture with minimal parameter variation, significant variations in soil phyla abundance were observed. Acidobacteria dominated across all samples, but linear discriminant analysis revealed distinct phyla compositions. At the genus level, Geobacter, Verticiella, and Glaciihabitans were most abundant in S11, S7, and S9 samples, respectively. However, the relative abundance of phyla in the soil samples from Yt, LP, and DS sites varies significantly. But the difference in bacterial community at genus level resolution was not significant at p value 0.05 level. These findings indicate that pruning and skiffing primarily impact on the relative abundance of soil phyla, not microbial diversity. Understanding the soil microbiota in relation to tea cultivation practices through metagenomics can pave the way for developing new microbial consortia for an integrated crop management system in tea cultivation.
{"title":"Analysing the Metagenomic Dynamics of Soil Microbiota Affected by Tea Pruning and Skiffing Methods in Tea Plantations of Dibrugarh, Assam, India.","authors":"Pritam Chattopadhyay, Irani Biswas, Goutam Banerjee","doi":"10.1007/s12088-024-01382-8","DOIUrl":"10.1007/s12088-024-01382-8","url":null,"abstract":"<p><p>Beginning with the centralization of young tea (Yt) to encourage low branch growth, subsequent light pruning (LP) and deep skiffing (DS) techniques are employed to promote branch spread, ensuring an ideal leaf area index and manageable plucking height. This study investigates the effects of LP and DS compared to Yt on soil biota, a previously unexplored topic. Soil samples from Yt, LP, and DS sites within the Rajgarh Tea Estate in Assam, India, were analyzed for standard parameters and metagenomic DNA using Illumina sequencing. While all samples exhibited a clay loam texture with minimal parameter variation, significant variations in soil phyla abundance were observed. Acidobacteria dominated across all samples, but linear discriminant analysis revealed distinct phyla compositions. At the genus level, <i>Geobacter, Verticiella</i>, and <i>Glaciihabitans</i> were most abundant in S11, S7, and S9 samples, respectively. However, the relative abundance of phyla in the soil samples from Yt, LP, and DS sites varies significantly. But the difference in bacterial community at genus level resolution was not significant at p value 0.05 level. These findings indicate that pruning and skiffing primarily impact on the relative abundance of soil phyla, not microbial diversity. Understanding the soil microbiota in relation to tea cultivation practices through metagenomics can pave the way for developing new microbial consortia for an integrated crop management system in tea cultivation.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"2015-2020"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12711606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2024-09-27DOI: 10.1007/s12088-024-01402-7
Asmita Dhimmar, Raghu Solanki, Sunita Patel, Pramod B Shinde
Zinc oxide nanoparticles (ZnO-NPs) are recognized as highly promising materials with applications in diverse fields, from therapeutics to agriculture. Hence, the present study aimed to biosynthesize ZnO-NPs employing the endophytic Streptomyces sp. 4VPT5-9 isolated from the halophytic plant Salicornia brachiata and evaluate the biological activity against plant pathogen Fusarium oxysporum NCIM 1008 and human breast (MDA-MB-231) and colorectal cancer (HCT-116) cell lines. The cell-free supernatant of the strain 4VPT5-9 was used as a greener attempt for the biosynthesis of ZnO-NPs. Biosynthesized ZnO-NPs exhibited an absorption peak at 287 nm. The hexagonal crystalline structure of the biosynthesized ZnO-NPs was validated through X-ray diffraction studies. These biosynthesized ZnO-NPs exhibited an irregular shape and varied in size, ranging between 120 and 150 nm with d-spacing value 0.26 nm. Moreover, FI-IR analysis showed different absorption peaks confirming the presence of different functional groups and formation of biosynthesized ZnO-NPs. XPS analysis confirmed the presence of Zn(II)O at different varied bending energies. The antifungal assay revealed that biosynthesized ZnO-NPs showed a pronounced inhibitory zone (12 mm) and the least MIC value of 60 µg/mL against plant pathogen F. oxysporum NCIM 1008. Moreover, the biosynthesized ZnO-NPs showed significant anticancer activity against MDA-MB-231 human breast cancer and HCT-116 human colorectal cell lines in a dose- and time-dependent manner. From this study, it is evident that an eco-conscious approach could pave a novel path for biosynthesis of ZnO-NPs through a halophytic plant-associated actinomycetes.
{"title":"Investigation of Antifungal and Anticancer Property of Zinc Oxide Nanoparticles Prepared Through Bioinspired Synthesis Using Endophytic Streptomyces Derived from Halophyte <i>Salicornia brachiata</i> Roxb.","authors":"Asmita Dhimmar, Raghu Solanki, Sunita Patel, Pramod B Shinde","doi":"10.1007/s12088-024-01402-7","DOIUrl":"10.1007/s12088-024-01402-7","url":null,"abstract":"<p><p>Zinc oxide nanoparticles (ZnO-NPs) are recognized as highly promising materials with applications in diverse fields, from therapeutics to agriculture. Hence, the present study aimed to biosynthesize ZnO-NPs employing the endophytic <i>Streptomyces</i> sp. 4VPT5-9 isolated from the halophytic plant <i>Salicornia brachiata</i> and evaluate the biological activity against plant pathogen <i>Fusarium oxysporum</i> NCIM 1008 and human breast (MDA-MB-231) and colorectal cancer (HCT-116) cell lines. The cell-free supernatant of the strain 4VPT5-9 was used as a greener attempt for the biosynthesis of ZnO-NPs. Biosynthesized ZnO-NPs exhibited an absorption peak at 287 nm. The hexagonal crystalline structure of the biosynthesized ZnO-NPs was validated through X-ray diffraction studies. These biosynthesized ZnO-NPs exhibited an irregular shape and varied in size, ranging between 120 and 150 nm with d-spacing value 0.26 nm. Moreover, FI-IR analysis showed different absorption peaks confirming the presence of different functional groups and formation of biosynthesized ZnO-NPs. XPS analysis confirmed the presence of Zn(II)O at different varied bending energies. The antifungal assay revealed that biosynthesized ZnO-NPs showed a pronounced inhibitory zone (12 mm) and the least MIC value of 60 µg/mL against plant pathogen <i>F. oxysporum</i> NCIM 1008. Moreover, the biosynthesized ZnO-NPs showed significant anticancer activity against MDA-MB-231 human breast cancer and HCT-116 human colorectal cell lines in a dose- and time-dependent manner. From this study, it is evident that an eco-conscious approach could pave a novel path for biosynthesis of ZnO-NPs through a halophytic plant-associated actinomycetes.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1972-1984"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712273/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Natural interaction among the endosymbiont microorganisms specifically fungi with plants have been noticed with a great utility. It has been observed that there is presence of fungal endophytes in most of the plant tested for isolation of endophytic association. Such fungi have received attention recently due to their capacity to produce several unique bioactive chemicals that were previously unknown to biological systems. These endophytes could be an important source of secondary metabolites that can be explored for discovery of novel compounds which can be used as medicine or growth enhancers of plants or animals. The secondary metabolites from endophytic fungi have been reported for their antimicrobial, antioxidant, anticancer, and antidiabetic activity and offer protection against pathogens and pests and improve plant survival during the stress. The current review article highlights the significance of biologically active substances obtained from fungal diverse endophytes associated with plants.
{"title":"The Potential of Fungal Endophytes in Plants: Sources of Bioactive Compounds.","authors":"Sagar Vishwakarma, Vijeta Chaudhry, Sumit Chand, Kalpana Sagar, Kartikey Kumar Gupta, Nitin Bhardwaj, Rajendra Prasad, Pankaj Kumar, Harish Chandra","doi":"10.1007/s12088-024-01406-3","DOIUrl":"10.1007/s12088-024-01406-3","url":null,"abstract":"<p><p>Natural interaction among the endosymbiont microorganisms specifically fungi with plants have been noticed with a great utility. It has been observed that there is presence of fungal endophytes in most of the plant tested for isolation of endophytic association. Such fungi have received attention recently due to their capacity to produce several unique bioactive chemicals that were previously unknown to biological systems. These endophytes could be an important source of secondary metabolites that can be explored for discovery of novel compounds which can be used as medicine or growth enhancers of plants or animals. The secondary metabolites from endophytic fungi have been reported for their antimicrobial, antioxidant, anticancer, and antidiabetic activity and offer protection against pathogens and pests and improve plant survival during the stress. The current review article highlights the significance of biologically active substances obtained from fungal diverse endophytes associated with plants.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1813-1827"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712289/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145803562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Unsaturated fatty acids serve a crucial role, enhancing the fluidity of microorganism membranes during fermentation which improves their nutrient assimilation besides contributing to the mouthfeel by influencing sensory aspects such as body, texture, and smoothness of wine. In the present study, three fermentation parameters i.e. °Brix, inoculum (Saccharomyces cerevisiae strain MK680910) concentration and oleic acid concentration were optimized by response surface methodology (RSM) to obtain maximum ethanol concentration. The fermentation of black grapes (hybrid H27) was carried out using S. cerevisiae MK680910 under the runs suggested by RSM to optimize the above mentioned three fermentation parameters. The solutions revealed that 17.6°Brix, 5.9% (v/v) inoculum (S. cerevisiae strain MK680910) concentration and 8.08 mg/L oleic acid concentration produces 9.413% (v/v) ethanol concentration with fermentation efficiency of 73.492% and 1.295 g/100 mL residual sugars. Validation of ethanolic fermentation led to 9.478% (v/v) ethanol concentration with fermentation efficiency of 73.540%; which shows that the model is well fitted. Microoxygenation (MOX) involves controlled exposing wine to limited amounts of oxygen during aging for the development of favorable attributes thus enhancing the overall quality of the wine in terms of stabilizing colour, enriching aroma profiles, and adding layers of complexity to the finished product. In the present study, total phenols were increased from 217.5 mg/100 mL of control to 297.5 mg/100 ml of 0.025 LPM incremental dose over three months of MOX treatment. The highest sensory score of 8.05 ± 0.14 was obtained for 0.025 LPM incremental treatment. Volatile profiling of wines through Gas chromatography mass spectrometry reported the presence of 5 more volatile sensory components with the use of 0.025 LPM incremental dose of red wine microoxygenation treatment besides glycerine, alcohols and organic acids found in control.
Supplementary information: The online version supplementary material available at 10.1007/s12088-024-01357-9.
{"title":"Effect of Oleic Acid Supplementation and Microoxygenation on Volatilome of Wine Prepared from Grape Hybrid H27 Using <i>S. cerevisiae</i> MK680910.","authors":"Preetiman Kaur, Gurvinder Singh Kocher, Keshani Bhushan","doi":"10.1007/s12088-024-01357-9","DOIUrl":"10.1007/s12088-024-01357-9","url":null,"abstract":"<p><p>Unsaturated fatty acids serve a crucial role, enhancing the fluidity of microorganism membranes during fermentation which improves their nutrient assimilation besides contributing to the mouthfeel by influencing sensory aspects such as body, texture, and smoothness of wine. In the present study, three fermentation parameters i.e. °Brix, inoculum (<i>Saccharomyces cerevisiae</i> strain MK680910) concentration and oleic acid concentration were optimized by response surface methodology (RSM) to obtain maximum ethanol concentration. The fermentation of black grapes (hybrid H27) was carried out using <i>S. cerevisiae</i> MK680910 under the runs suggested by RSM to optimize the above mentioned three fermentation parameters. The solutions revealed that 17.6°Brix, 5.9% (v/v) inoculum (<i>S. cerevisiae</i> strain MK680910) concentration and 8.08 mg/L oleic acid concentration produces 9.413% (v/v) ethanol concentration with fermentation efficiency of 73.492% and 1.295 g/100 mL residual sugars. Validation of ethanolic fermentation led to 9.478% (v/v) ethanol concentration with fermentation efficiency of 73.540%; which shows that the model is well fitted. Microoxygenation (MOX) involves controlled exposing wine to limited amounts of oxygen during aging for the development of favorable attributes thus enhancing the overall quality of the wine in terms of stabilizing colour, enriching aroma profiles, and adding layers of complexity to the finished product. In the present study, total phenols were increased from 217.5 mg/100 mL of control to 297.5 mg/100 ml of 0.025 LPM incremental dose over three months of MOX treatment. The highest sensory score of 8.05 ± 0.14 was obtained for 0.025 LPM incremental treatment. Volatile profiling of wines through Gas chromatography mass spectrometry reported the presence of 5 more volatile sensory components with the use of 0.025 LPM incremental dose of red wine microoxygenation treatment besides glycerine, alcohols and organic acids found in control.</p><p><strong>Supplementary information: </strong>The online version supplementary material available at 10.1007/s12088-024-01357-9.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1961-1971"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2024-09-30DOI: 10.1007/s12088-024-01392-6
Davi de Lacerda Coriolano, Jaqueline Barbosa de Souza, Iago Dillion Lima Cavalcanti, Isabella Macário Ferro Cavalcanti
Bacterial infections have become a global public health problem in recent decades, mainly due to infections caused by Gram-negative bacteria with antibiotic resistance profiles, which were responsible for over 3 million deaths in 2019. Polymyxin B (PMB) and polymyxin E (PME or colistin) are cyclic cationic polypeptide antimicrobials that have re-emerged in clinical practice due to the high rates of morbidity and mortality in infections caused by Gram-negative multidrug-resistant or extensively drug-resistant. Although polymyxins have antibacterial potential, they still have low stability and adverse effects, thus limiting their administration. To overcome these limitations, the use of controlled release systems such as liposomes, nanoparticles, and nanotubes is a viable strategy. Therefore, the objective of this review article is to present recent studies that address the antibacterial activity of PMB and PME encapsulated in nanocarriers against Gram-negative bacteria and to highlight the advantages of these nanocarriers and how they can overcome polymyxin limitations and bacterial resistance to polymyxin, as well as increasing drugs efficacy and safety. The preparation of this narrative review was based on the following steps: identification of the theme, establishment of inclusion and exclusion criteria, analysis and selection of articles, interpretation of data and results, and the writing of this article. Nanoparticles, electrostatic nanocomplexes, nanostructured lipid carriers, liposomes, and halloysite nanotubes can enhance bacterial activity from both PMB and PME, reducing minimum inhibitory concentration, inhibiting and eradicating biofilm, as well as prolonging polymyxins activity, reducing toxicity, and improving bioavailability. The strategy of encapsulation of polymyxin in nanocarriers has demonstrated a significant enhancement in polymyxin activity and pharmacokinetics, resulting in elevated therapeutic efficacy. Therefore, nanocarriers containing polymyxin emerge as a promising and innovative strategy to address this global challenge in public health.
{"title":"Antibacterial Activity of Polymyxins Encapsulated in Nanocarriers Against Gram-Negative Bacteria.","authors":"Davi de Lacerda Coriolano, Jaqueline Barbosa de Souza, Iago Dillion Lima Cavalcanti, Isabella Macário Ferro Cavalcanti","doi":"10.1007/s12088-024-01392-6","DOIUrl":"https://doi.org/10.1007/s12088-024-01392-6","url":null,"abstract":"<p><p>Bacterial infections have become a global public health problem in recent decades, mainly due to infections caused by Gram-negative bacteria with antibiotic resistance profiles, which were responsible for over 3 million deaths in 2019. Polymyxin B (PMB) and polymyxin E (PME or colistin) are cyclic cationic polypeptide antimicrobials that have re-emerged in clinical practice due to the high rates of morbidity and mortality in infections caused by Gram-negative multidrug-resistant or extensively drug-resistant. Although polymyxins have antibacterial potential, they still have low stability and adverse effects, thus limiting their administration. To overcome these limitations, the use of controlled release systems such as liposomes, nanoparticles, and nanotubes is a viable strategy. Therefore, the objective of this review article is to present recent studies that address the antibacterial activity of PMB and PME encapsulated in nanocarriers against Gram-negative bacteria and to highlight the advantages of these nanocarriers and how they can overcome polymyxin limitations and bacterial resistance to polymyxin, as well as increasing drugs efficacy and safety. The preparation of this narrative review was based on the following steps: identification of the theme, establishment of inclusion and exclusion criteria, analysis and selection of articles, interpretation of data and results, and the writing of this article. Nanoparticles, electrostatic nanocomplexes, nanostructured lipid carriers, liposomes, and halloysite nanotubes can enhance bacterial activity from both PMB and PME, reducing minimum inhibitory concentration, inhibiting and eradicating biofilm, as well as prolonging polymyxins activity, reducing toxicity, and improving bioavailability. The strategy of encapsulation of polymyxin in nanocarriers has demonstrated a significant enhancement in polymyxin activity and pharmacokinetics, resulting in elevated therapeutic efficacy. Therefore, nanocarriers containing polymyxin emerge as a promising and innovative strategy to address this global challenge in public health.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1799-1812"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712259/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804473","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2024-10-19DOI: 10.1007/s12088-024-01412-5
Xiao Tan, Xinlei Li, Honglei Wang
In this study, high-throughput sequencing (HTS) was used to demonstrate the microbial community diversity and succession of the casing soil during Oudemansiella raphanipes cultivation. The abundance and diversity of bacteria and fungi were the highest in the original sample of vegetable soil, and then decreased in casing soil, but they increased at the end of the mushroom formation. As the mushroom formation progressed, the abundance of some bacteria such as Massilia, Sphingomonas, and Cupriavidus increased, and they are often found in heavy metal contaminated soils. In terms of fungi, the dominant fungi in the vegetable soil and at the end of the mushroom formation stage were Thermoascus, and the abundance of some plant and animal pathogens increased in the first and second mushroom formation stages, such as Candida, Aspergillus, Trichoderma, and Chaetomium. The above results showed a decrease in the number of microbial species and an increase of harmful microorganisms, which might inhibit the growth of mushroom. Furthermore, we disinfected and sterilized the casing soil to investigate the effect of different treatments of casing soil on the growth and quality of Oudemansiella raphanipes. Results showed that the casing soil was beneficial for the cultivation of Oudemansiella raphanipes, but microorganisms in the casing soil might not be necessary for the growth of mushroom. Sterilization treatment of the casing soil could improve yield and quality more than conventional disinfection treatment. In future studies, different matrix materials can be explored to replace soil cover to achieve soilless cultivation which is more efficient and hygienic.
{"title":"Microbial Community Dynamics in Casing Soil and Impact on <i>Oudemansiella raphanipes</i> during Cultivation.","authors":"Xiao Tan, Xinlei Li, Honglei Wang","doi":"10.1007/s12088-024-01412-5","DOIUrl":"https://doi.org/10.1007/s12088-024-01412-5","url":null,"abstract":"<p><p>In this study, high-throughput sequencing (HTS) was used to demonstrate the microbial community diversity and succession of the casing soil during <i>Oudemansiella raphanipes</i> cultivation. The abundance and diversity of bacteria and fungi were the highest in the original sample of vegetable soil, and then decreased in casing soil, but they increased at the end of the mushroom formation. As the mushroom formation progressed, the abundance of some bacteria such as <i>Massilia, Sphingomonas</i>, and <i>Cupriavidus</i> increased, and they are often found in heavy metal contaminated soils. In terms of fungi, the dominant fungi in the vegetable soil and at the end of the mushroom formation stage were <i>Thermoascus</i>, and the abundance of some plant and animal pathogens increased in the first and second mushroom formation stages, such as <i>Candida</i>, <i>Aspergillus</i>, <i>Trichoderma</i>, and <i>Chaetomium.</i> The above results showed a decrease in the number of microbial species and an increase of harmful microorganisms, which might inhibit the growth of mushroom. Furthermore, we disinfected and sterilized the casing soil to investigate the effect of different treatments of casing soil on the growth and quality of <i>Oudemansiella raphanipes.</i> Results showed that the casing soil was beneficial for the cultivation of <i>Oudemansiella raphanipes,</i> but microorganisms in the casing soil might not be necessary for the growth of mushroom. Sterilization treatment of the casing soil could improve yield and quality more than conventional disinfection treatment. In future studies, different matrix materials can be explored to replace soil cover to achieve soilless cultivation which is more efficient and hygienic.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1995-2003"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712254/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2024-10-25DOI: 10.1007/s12088-024-01413-4
Sourabh Dutta, Anwesha Chakraborty, Manisha Biswal, Ambika Sharma, Vanita Suri, Pallab Ray
Preterm mother-neonate dyads are often exposed to broad-spectrum antibiotics. We studied preterm dyads for multidrug-resistant potentially pathogenic bacteria (MDR-PPB).To determine colonisation rates of MDR-PPB in mother's milk and neonatal oral and rectal swabs and identify genetically identical strains across the 3 samples. We enrolled lactating mother-neonate dyads, and cultured milk and neonatal oral, rectal swabs under aseptic conditions. We identified bacteria using MALDI-TOF, focusing on a panel of 13 neonatal pathogens of interest. Sensitivity was tested using Vitek2. If the milk, oral, and rectal swab samples from a mother-neonate dyad showed the same species and antibiogram, multi-locus sequence type (MLST) was performed. Of 130 dyads screened, we enrolled 100. 14 milk samples (from 14 mothers) had pathogens of interest, including 9 (64%) MDR bacteria. 82 isolates were grown from the oral swabs (77 neonates), of which 58 (70.7%) were MDR. 130 isolates were grown from the rectal swabs (96 neonates), of which 104 (80%) were MDR. Two mother-neonate dyads had MDR Escherichia coli and Klebsiella pneumoniae species cultured from all three samples with identical antibiograms. On MLST, DNA sequencing analysis of the PCR products showed no variation at all 7 loci of E. coli (Sequence Type-405), whereas, with K. pneumoniae, variations were observed in 4 loci (infB, mdh, phoE,rpoB). An alarming proportion of preterm mother's milk, oral swab and rectal swabs have MDR-PPB. MLST suggested that a pathogenic strain of E. coli was transmitted from mother's milk to the neonate's gut.
{"title":"Multidrug-Resistant, Potentially Pathogenic Bacteria in Mother's Milk, and Neonatal Oral and Rectal Swabs of Preterm Mother-Neonate Dyads.","authors":"Sourabh Dutta, Anwesha Chakraborty, Manisha Biswal, Ambika Sharma, Vanita Suri, Pallab Ray","doi":"10.1007/s12088-024-01413-4","DOIUrl":"10.1007/s12088-024-01413-4","url":null,"abstract":"<p><p>Preterm mother-neonate dyads are often exposed to broad-spectrum antibiotics. We studied preterm dyads for multidrug-resistant potentially pathogenic bacteria (MDR-PPB).To determine colonisation rates of MDR-PPB in mother's milk and neonatal oral and rectal swabs and identify genetically identical strains across the 3 samples. We enrolled lactating mother-neonate dyads, and cultured milk and neonatal oral, rectal swabs under aseptic conditions. We identified bacteria using MALDI-TOF, focusing on a panel of 13 neonatal pathogens of interest. Sensitivity was tested using Vitek2. If the milk, oral, and rectal swab samples from a mother-neonate dyad showed the same species and antibiogram, multi-locus sequence type (MLST) was performed. Of 130 dyads screened, we enrolled 100. 14 milk samples (from 14 mothers) had pathogens of interest, including 9 (64%) MDR bacteria. 82 isolates were grown from the oral swabs (77 neonates), of which 58 (70.7%) were MDR. 130 isolates were grown from the rectal swabs (96 neonates), of which 104 (80%) were MDR. Two mother-neonate dyads had MDR <i>Escherichia coli</i> and <i>Klebsiella pneumoniae</i> species cultured from all three samples with identical antibiograms. On MLST, DNA sequencing analysis of the PCR products showed no variation at all 7 loci of <i>E. coli</i> (Sequence Type-405), whereas, with <i>K. pneumoniae</i>, variations were observed in 4 loci (infB, mdh, phoE,rpoB). An alarming proportion of preterm mother's milk, oral swab and rectal swabs have MDR-PPB. MLST suggested that a pathogenic strain of <i>E. coli</i> was transmitted from mother's milk to the neonate's gut.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"2004-2014"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712266/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2024-10-08DOI: 10.1007/s12088-024-01407-2
Gulfishan Khan, Srikrishna Subramanian, Varsha Tripathi, Saurabh Singh, Natesan Manickam
Polycyclic aromatic hydrocarbons (PAHs) are biodegraded primarily by bacterial activities from polluted environments. From an oily sludge disposals site an Achromobacter xylosoxidans bacterium (designated as strain IITR150) was isolated with capability to grow and degrade multiple PAHs. Strain IITR150 was found to utilize naphthalene, phenanthrene, anthracene, benz(a)pyrene, benz(a)anthracene, and fluoranthene as the carbon source for its growth. Initially, the bacterium was screened based on its ability to turn indole into indigo and formed metabolites of the indole pathway such as indoxyl, isatin and indirubin. A 1014 bp gene encoding for a naphthalene 1,2-dioxygenase was found to initiate the biodegradation of naphthalene to have 42.85% homology to reported genes. Whole genome sequencing of A. xylosoxidans IITR150 had showed 5.9 Mb genome size containing 5625 predicted CDS. Among 5625 predicted CDS, cytochrome P450, catechol 2,3-dioxygenase (catE), naphthalene 1,2-dioxygenase system ferredoxin-NAD(P) ( +) reductase component (nahA), naphthalene 1,2-dioxygenase system, and ferredoxin components (nahB) genes were identified that indicated the metabolic potential of the bacterium for utilization of different aromatic compounds. Besides identification of PAHs degrading genes along with genomic insights suggests the robustness of the bacteria. Also, a cytochrome P450 (cytP450) enzymes that play a pivotal role in the detoxification of xenobiotics was found in IITR150, when aligned with three other cytP450 showed over 99.0% similarity at amino acid level. In conclusion, experimental and whole genome analysis provide capabilities of strain IITR150 involved in PAHs metabolism which could be useful in biodegradation of mixed PAHs contaminated soils.
Supplementary information: The online version contains supplementary material available at 10.1007/s12088-024-01407-2.
多环芳烃(PAHs)主要通过污染环境中的细菌活性进行生物降解。从含油污泥处理场分离出一株具有生长和降解多种多环芳烃能力的木氧化无色杆菌(菌株IITR150)。菌株IITR150利用萘、菲、蒽、苯并(a)芘、苯并(a)蒽和氟蒽作为其生长的碳源。最初,这种细菌是根据其将吲哚转化为靛蓝的能力进行筛选的,并形成吲哚途径的代谢物,如吲哚基、isatin和靛玉红。发现一个编码萘1,2-双加氧酶的1014 bp基因启动萘的生物降解,与报道的基因有42.85%的同源性。木索酸A. xylosoxidans IITR150的全基因组测序结果显示,其基因组大小为5.9 Mb,内含5625个预测CDS。在5625个预测的CDS中,鉴定出细胞色素P450、儿茶酚2,3-双加氧酶(catE)、萘1,2-双加氧酶系统铁氧还蛋白- nad (P)(+)还原酶组分(nahA)、萘1,2-双加氧酶系统和铁氧还蛋白组分(nahB)基因,表明该细菌利用不同芳香族化合物的代谢潜力。此外,多环芳烃降解基因的鉴定以及基因组的见解表明了细菌的稳健性。此外,在IITR150中发现了一个细胞色素P450 (cytP450)酶,该酶在异种生物解毒中起关键作用,当与其他三个cytP450在氨基酸水平上比对时,其相似性超过99.0%。结果表明,菌株IITR150具有参与多环芳烃代谢的能力,可用于混合多环芳烃污染土壤的生物降解。补充信息:在线版本包含补充资料,下载地址:10.1007/s12088-024-01407-2。
{"title":"Characterization of Multiple Polycyclic Aromatic Hydrocarbons (PAHs) Degrading <i>Achromobacter xylosoxidans</i> IITR150: Novel Insights from Whole Genome Analysis.","authors":"Gulfishan Khan, Srikrishna Subramanian, Varsha Tripathi, Saurabh Singh, Natesan Manickam","doi":"10.1007/s12088-024-01407-2","DOIUrl":"10.1007/s12088-024-01407-2","url":null,"abstract":"<p><p>Polycyclic aromatic hydrocarbons (PAHs) are biodegraded primarily by bacterial activities from polluted environments. From an oily sludge disposals site an <i>Achromobacter xylosoxidans</i> bacterium (designated as strain IITR150) was isolated with capability to grow and degrade multiple PAHs. Strain IITR150 was found to utilize naphthalene, phenanthrene, anthracene, benz(a)pyrene, benz(a)anthracene, and fluoranthene as the carbon source for its growth. Initially, the bacterium was screened based on its ability to turn indole into indigo and formed metabolites of the indole pathway such as indoxyl, isatin and indirubin. A 1014 bp gene encoding for a naphthalene 1,2-dioxygenase was found to initiate the biodegradation of naphthalene to have 42.85% homology to reported genes. Whole genome sequencing of <i>A. xylosoxidans</i> IITR150 had showed 5.9 Mb genome size containing 5625 predicted CDS. Among 5625 predicted CDS, cytochrome P450, catechol 2,3-dioxygenase (<i>cat</i>E), naphthalene 1,2-dioxygenase system ferredoxin-NAD(P) ( +) reductase component (<i>nah</i>A), naphthalene 1,2-dioxygenase system, and ferredoxin components (<i>nah</i>B) genes were identified that indicated the metabolic potential of the bacterium for utilization of different aromatic compounds. Besides identification of PAHs degrading genes along with genomic insights suggests the robustness of the bacteria. Also, a cytochrome P450 (<i>cyt</i>P450) enzymes that play a pivotal role in the detoxification of xenobiotics was found in IITR150, when aligned with three other <i>cyt</i>P450 showed over 99.0% similarity at amino acid level. In conclusion, experimental and whole genome analysis provide capabilities of strain IITR150 involved in PAHs metabolism which could be useful in biodegradation of mixed PAHs contaminated soils.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12088-024-01407-2.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 4","pages":"1985-1994"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712251/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145804507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}