The phytopathogenic oomycete Phytopythium helicoides, previously known as Pythium helicoides, has emerged as a new threat to the Shatangju citrus cultivar (Citrus reticulata cv. Shatangju; '' in Chinese) in southern China. To enable rapid diagnosis and control of the leaf blight and stem rot caused by P. helicoides, we developed a visualized loop-mediated isothermal amplification (LAMP) assay targeting the β-tubulin gene of the pathogen. Using a carefully selected set of primers and optimized reaction conditions at 60 °C for 60 min, the LAMP assay can specifically detect the pathogen among various citrus-associated phytopathogens. The assay demonstrated high sensitivity, detecting as little as 30 pg of the pathogen DNA, comparable to the sensitivity of quantitative polymerase chain reaction (qPCR). We validated the practical application of this LAMP assay for diagnosing infections in citrus leaves and strawberry crowns. This newly developed LAMP assay offers a specific, sensitive, and rapid detection tool for P. helicoides, aiding in the control of Shatangju citrus leaf blight and stem rot, as well as other related crop diseases like strawberry crown rot.
{"title":"Rapid detection of the phytopathogenic oomycete Phytopythium helicoides with a visualized loop-mediated isothermal amplification assay.","authors":"Le-Yao Ren, Ke Wen, Bao-Ping Cheng, Jing-Hao Jin, Vaibhav Srivastava, Xiao-Ren Chen","doi":"10.1007/s42770-024-01578-6","DOIUrl":"10.1007/s42770-024-01578-6","url":null,"abstract":"<p><p>The phytopathogenic oomycete Phytopythium helicoides, previously known as Pythium helicoides, has emerged as a new threat to the Shatangju citrus cultivar (Citrus reticulata cv. Shatangju; '' in Chinese) in southern China. To enable rapid diagnosis and control of the leaf blight and stem rot caused by P. helicoides, we developed a visualized loop-mediated isothermal amplification (LAMP) assay targeting the β-tubulin gene of the pathogen. Using a carefully selected set of primers and optimized reaction conditions at 60 °C for 60 min, the LAMP assay can specifically detect the pathogen among various citrus-associated phytopathogens. The assay demonstrated high sensitivity, detecting as little as 30 pg of the pathogen DNA, comparable to the sensitivity of quantitative polymerase chain reaction (qPCR). We validated the practical application of this LAMP assay for diagnosing infections in citrus leaves and strawberry crowns. This newly developed LAMP assay offers a specific, sensitive, and rapid detection tool for P. helicoides, aiding in the control of Shatangju citrus leaf blight and stem rot, as well as other related crop diseases like strawberry crown rot.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"563-572"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142791082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-12-02DOI: 10.1007/s42770-024-01573-x
Hao Liu, Shumin Wang, Xin Yu, Shuguang Sun, Yingzhen Su
Some natural products have been found to have a positive effect on the treatment of Type 2 Diabetes Mellitus (T2DM). The effective mechanism by which these natural products work may be attributed to their ability to alter the gut microbiome. In this study, considering the beneficial properties of resveratrol for T2DM, the mechanism of resveratrol in releasing of T2DM, the correlation between the apparent traits of resveratrol in T2DM mice and the changes in intestinal flora structure were explored. The intervention of resveratrol in different dose did effectively improve the apparent T2DM symptoms in mice, including reduced fasting blood glucose, enhance to both the insulin tolerance and glucose tolerance. Simultaneously, resveratrol can effectively ameliorate the pathological condition of the colon and rectum in T2DM mice, leading to a reduction in intestinal villi swelling and fat vacuoles. The intervention of resveratrol led to changes in the gut flora structure of T2DM mice. Erysipelas and Ileibacterium are crucial taxa of resveratrol involved in maintaining the balance of the gut microbiota. The abundance of Erysipelotrichaceae and Ileibacterium was significantly elevated under the treatment of resveratrol, and the compose of the gut microbiota was more inclined to healthy mice. T2DM symptoms could be alleviated by resveratrol through different mechanisms compared to metformin intervention.
{"title":"Effect of Resveratrol on the intestinal microbiota in Type2 diabetes Mellitus mice.","authors":"Hao Liu, Shumin Wang, Xin Yu, Shuguang Sun, Yingzhen Su","doi":"10.1007/s42770-024-01573-x","DOIUrl":"10.1007/s42770-024-01573-x","url":null,"abstract":"<p><p>Some natural products have been found to have a positive effect on the treatment of Type 2 Diabetes Mellitus (T2DM). The effective mechanism by which these natural products work may be attributed to their ability to alter the gut microbiome. In this study, considering the beneficial properties of resveratrol for T2DM, the mechanism of resveratrol in releasing of T2DM, the correlation between the apparent traits of resveratrol in T2DM mice and the changes in intestinal flora structure were explored. The intervention of resveratrol in different dose did effectively improve the apparent T2DM symptoms in mice, including reduced fasting blood glucose, enhance to both the insulin tolerance and glucose tolerance. Simultaneously, resveratrol can effectively ameliorate the pathological condition of the colon and rectum in T2DM mice, leading to a reduction in intestinal villi swelling and fat vacuoles. The intervention of resveratrol led to changes in the gut flora structure of T2DM mice. Erysipelas and Ileibacterium are crucial taxa of resveratrol involved in maintaining the balance of the gut microbiota. The abundance of Erysipelotrichaceae and Ileibacterium was significantly elevated under the treatment of resveratrol, and the compose of the gut microbiota was more inclined to healthy mice. T2DM symptoms could be alleviated by resveratrol through different mechanisms compared to metformin intervention.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"447-463"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142766089","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-11-14DOI: 10.1007/s42770-024-01559-9
Saruanna Millena Dos Santos Clemente, Samuel Fernando Dos Santos, Priscilla Régia de Andrade Calaça, Maria Taciana Cavalcanti Vieira Soares, Webert Aurino da Silva, Renata Pimentel Bandeira de Melo, Rinaldo Aparecido Mota, Mércia Rodrigues Barros
<p><p>Campylobacteriosis is among the most reported zoonoses in the world, caused by species of Campylobacter, this disease is characterized by gastroenteritis in humans. The main species involved is Campylobacter jejuni, followed by Campylobacter coli. Contaminated chicken meat is often identified as an important source of infection related to human cases and Brazil is the largest exporter of chicken meat in the world, which makes the characterization of brazilian isolates crucial for the establishment of control measures. The objective was to evaluate the contamination of chilled and frozen carcasses sold in the Northeast of Brazil, by Campylobacter species, identify virulence genes, evaluate bacterial resistance to antibiotics and verify the antimicrobial action of the Crude Extract Containing Enterocins (CECE) produced by a probiotic strain of Enterococcus faecium. In this study, 12 chilled carcasses and 12 frozen carcasses were collected, sold retail in supermarkets. The following regions of the carcass were sampled: breast skin, wing skin, belly skin, neck skin, gizzard and liver. Samples of chicken carcasses were analyzed following ISO 10272-2 guidelines for the isolation of Campylobacter spp. The isolates were tested by PCR to identify genus, species C. jejuni, C. coli and C. lari and genes cdtA, cdtB, cdtC, sodB, dnaJ, cmeA, cmeB, cmeC. The assessment of susceptibility to antibiotics was carried out using the standard disk diffusion method and the antimicrobial activity of CECE was determined using the Minimum Inhibitory Concentration (MIC), the methodologies followed the recommendations and cutoff points according to EUCAST and CLSI. A total of 376 isolates of Campylobacter spp. were obtained, among these, 26 (7.0%) were positive for C. jejuni and no isolates were detected for C. coli and C. lari. The highest frequency of C. jejuni was obtained in chilled carcasses with 23 isolates (88.5%, p < 0.0001), in frozen carcasses three isolates were obtained (11.5%). The most frequency site of C. jejuni was the chest skin (7/27.0%), followed by skin of the wing (6/23.0%), skin of the cloaca (5/19.0%), gizzard (4/15.0%), skin of the neck (2/8.0%) and liver (2/8.0%), no significant differences were found between the sites sampled. The gene frequency was determined in: cdtA (3/11.5%), cdtB (3/11.5%), cdtC (5/19.0%), sodB (9/34.5%), dnaJ (3/11.5%), cmeA (4/15.0%), cmeB (4/15.0%) and cmeC (4/15.0%). The three efflux pump genes were amplified in four isolates (15.3%) and all tested genes were amplified in three isolates (11.5%). All C. jejuni isolates (26/100.0%) were found to be multiresistant to three or more classes of antimicrobials. The index of multiple resistance to antimicrobial drugs (IRMA) ranged from 0.4 to 1.0 among isolates of C. jejuni. The antimicrobial activity of CECE was able to inhibit at least 98.5% of the growth of all C. jejuni isolates. Therefore, chilled chicken carcasses present a greater risk of contamination than frozen car
{"title":"Gene profile of virulence, antimicrobial resistance and action of enterocins in Campylobacter species isolated from broiler carcasses.","authors":"Saruanna Millena Dos Santos Clemente, Samuel Fernando Dos Santos, Priscilla Régia de Andrade Calaça, Maria Taciana Cavalcanti Vieira Soares, Webert Aurino da Silva, Renata Pimentel Bandeira de Melo, Rinaldo Aparecido Mota, Mércia Rodrigues Barros","doi":"10.1007/s42770-024-01559-9","DOIUrl":"10.1007/s42770-024-01559-9","url":null,"abstract":"<p><p>Campylobacteriosis is among the most reported zoonoses in the world, caused by species of Campylobacter, this disease is characterized by gastroenteritis in humans. The main species involved is Campylobacter jejuni, followed by Campylobacter coli. Contaminated chicken meat is often identified as an important source of infection related to human cases and Brazil is the largest exporter of chicken meat in the world, which makes the characterization of brazilian isolates crucial for the establishment of control measures. The objective was to evaluate the contamination of chilled and frozen carcasses sold in the Northeast of Brazil, by Campylobacter species, identify virulence genes, evaluate bacterial resistance to antibiotics and verify the antimicrobial action of the Crude Extract Containing Enterocins (CECE) produced by a probiotic strain of Enterococcus faecium. In this study, 12 chilled carcasses and 12 frozen carcasses were collected, sold retail in supermarkets. The following regions of the carcass were sampled: breast skin, wing skin, belly skin, neck skin, gizzard and liver. Samples of chicken carcasses were analyzed following ISO 10272-2 guidelines for the isolation of Campylobacter spp. The isolates were tested by PCR to identify genus, species C. jejuni, C. coli and C. lari and genes cdtA, cdtB, cdtC, sodB, dnaJ, cmeA, cmeB, cmeC. The assessment of susceptibility to antibiotics was carried out using the standard disk diffusion method and the antimicrobial activity of CECE was determined using the Minimum Inhibitory Concentration (MIC), the methodologies followed the recommendations and cutoff points according to EUCAST and CLSI. A total of 376 isolates of Campylobacter spp. were obtained, among these, 26 (7.0%) were positive for C. jejuni and no isolates were detected for C. coli and C. lari. The highest frequency of C. jejuni was obtained in chilled carcasses with 23 isolates (88.5%, p < 0.0001), in frozen carcasses three isolates were obtained (11.5%). The most frequency site of C. jejuni was the chest skin (7/27.0%), followed by skin of the wing (6/23.0%), skin of the cloaca (5/19.0%), gizzard (4/15.0%), skin of the neck (2/8.0%) and liver (2/8.0%), no significant differences were found between the sites sampled. The gene frequency was determined in: cdtA (3/11.5%), cdtB (3/11.5%), cdtC (5/19.0%), sodB (9/34.5%), dnaJ (3/11.5%), cmeA (4/15.0%), cmeB (4/15.0%) and cmeC (4/15.0%). The three efflux pump genes were amplified in four isolates (15.3%) and all tested genes were amplified in three isolates (11.5%). All C. jejuni isolates (26/100.0%) were found to be multiresistant to three or more classes of antimicrobials. The index of multiple resistance to antimicrobial drugs (IRMA) ranged from 0.4 to 1.0 among isolates of C. jejuni. The antimicrobial activity of CECE was able to inhibit at least 98.5% of the growth of all C. jejuni isolates. Therefore, chilled chicken carcasses present a greater risk of contamination than frozen car","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"237-250"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142614740","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-12-17DOI: 10.1007/s42770-024-01581-x
Tereza de Jesus Pinheiro Gomes Bandeira, Ana Leticia Sousa de Oliveira, Luis Fernando Pontes Martins, Rodrigo Moreira Matos, Sheryda Raynna Nobre Guedes Dos Santos, Mateus Cedro Lopes, Raimundo Tadeu Pires Sobreira, Hermano Alexandre Lima Rocha
Respiratory tract infection (RTI) is the most important cause of visiting both public and private medical care services. During the decade preceding Covid-19, in developing countries, there was a gap in the epidemiology of respiratory viral infections, probably due to the difficulty of detecting viral agents in clinical microbiology laboratories routine, at that time. In this context, the aim of this study was to describe the occurrence of virus, demographic factors associated and the likelihood of coinfections detection by multiplex PCR methods. The target also was to determine the involvement of respiratory viruses other than SARS-CoV-2 as agents of upper respiratory tract infections (URTIs) using rapid respiratory panels by multiplex real time PCR with flow chip methodology. Samples of SARSs patients, 530 in total, were tested between 2022 and 2023, obtained from nasopharyngeal swabs, nasopharyngeal exudates or nasopharyngeal aspirates. Of 530 tests, 30% was human rhinovirus, the most prevalent, followed by respiratory syncytial virus B (21.5%) and human adenovirus (17.4%). Among the total of positive samples, 83.8% belonged to patients aged between 0 and 10 years, 62.6% of whom were aged between 1 and 10 years. Multiple virus detection was found in 50.4% of the samples tested, 93.1% of which were from patients under the age of 18. Viral co-infection was evident in the finding and was higher (88.7%) in patients under the age of 18 yeas.
{"title":"Molecular detection of respiratory viruses: an observational study on respiratory co-infections in children and adults.","authors":"Tereza de Jesus Pinheiro Gomes Bandeira, Ana Leticia Sousa de Oliveira, Luis Fernando Pontes Martins, Rodrigo Moreira Matos, Sheryda Raynna Nobre Guedes Dos Santos, Mateus Cedro Lopes, Raimundo Tadeu Pires Sobreira, Hermano Alexandre Lima Rocha","doi":"10.1007/s42770-024-01581-x","DOIUrl":"10.1007/s42770-024-01581-x","url":null,"abstract":"<p><p>Respiratory tract infection (RTI) is the most important cause of visiting both public and private medical care services. During the decade preceding Covid-19, in developing countries, there was a gap in the epidemiology of respiratory viral infections, probably due to the difficulty of detecting viral agents in clinical microbiology laboratories routine, at that time. In this context, the aim of this study was to describe the occurrence of virus, demographic factors associated and the likelihood of coinfections detection by multiplex PCR methods. The target also was to determine the involvement of respiratory viruses other than SARS-CoV-2 as agents of upper respiratory tract infections (URTIs) using rapid respiratory panels by multiplex real time PCR with flow chip methodology. Samples of SARSs patients, 530 in total, were tested between 2022 and 2023, obtained from nasopharyngeal swabs, nasopharyngeal exudates or nasopharyngeal aspirates. Of 530 tests, 30% was human rhinovirus, the most prevalent, followed by respiratory syncytial virus B (21.5%) and human adenovirus (17.4%). Among the total of positive samples, 83.8% belonged to patients aged between 0 and 10 years, 62.6% of whom were aged between 1 and 10 years. Multiple virus detection was found in 50.4% of the samples tested, 93.1% of which were from patients under the age of 18. Viral co-infection was evident in the finding and was higher (88.7%) in patients under the age of 18 yeas.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"537-543"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142845981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2025-01-10DOI: 10.1007/s42770-024-01588-4
Letícia Sanfilippo Rojas, Michelle Guzmán de Fernandes, Andressa Cristina Ramaglia da Motta, Luiza Porteiro Carminato, Ana Caroline Zanatta, Gisele Lôbo-Hajdu, Paula Jimenez, Márcio Reis Custódio, Cristiane Cassiolato Pires Hardoim
Culture-dependent and -independent studies have provided access to symbiont genes and the functions they play for host sponges. Thus, this work investigates the diversity, presence of genes of pharmacological interest, biological activities and metabolome of the bacteria isolated from the sponges Aplysina caissara and Aplysina fulva collected on the southwestern Atlantic Coast. The genes for Polyketide Synthases types I and II and Nonribosomal Peptide Synthetases were screened in more than 200 bacterial strains obtained, from which around 40% were putatively novel. Twenty-two were positive for at least one of the genes screened. Among them, 12 exhibited antimicrobial activities and one inhibited the proliferation of cancer cells. The metabolic profiles of the 22 strains were analyzed by liquid chromatography with tandem mass spectrometry and molecular network. The Global Natural Products Social Molecular Networking MolNetEnhancer workflow provided a more comprehensive understanding of the metabolic profiles. The results revealed the existence of a wide range of metabolites, however more than half of the compounds could not be identified. It was further observed that the metabolic diversity among the strains varied primarily due to the cultivation medium used. Together the results obtained here revealed the pharmacological potential of the bacteria isolated from Aplysina species.
{"title":"Presence of polyketide synthases and nonribosomal peptide synthetase in culturable bacteria associated with Aplysina fulva and Aplysina caissara (Porifera).","authors":"Letícia Sanfilippo Rojas, Michelle Guzmán de Fernandes, Andressa Cristina Ramaglia da Motta, Luiza Porteiro Carminato, Ana Caroline Zanatta, Gisele Lôbo-Hajdu, Paula Jimenez, Márcio Reis Custódio, Cristiane Cassiolato Pires Hardoim","doi":"10.1007/s42770-024-01588-4","DOIUrl":"10.1007/s42770-024-01588-4","url":null,"abstract":"<p><p>Culture-dependent and -independent studies have provided access to symbiont genes and the functions they play for host sponges. Thus, this work investigates the diversity, presence of genes of pharmacological interest, biological activities and metabolome of the bacteria isolated from the sponges Aplysina caissara and Aplysina fulva collected on the southwestern Atlantic Coast. The genes for Polyketide Synthases types I and II and Nonribosomal Peptide Synthetases were screened in more than 200 bacterial strains obtained, from which around 40% were putatively novel. Twenty-two were positive for at least one of the genes screened. Among them, 12 exhibited antimicrobial activities and one inhibited the proliferation of cancer cells. The metabolic profiles of the 22 strains were analyzed by liquid chromatography with tandem mass spectrometry and molecular network. The Global Natural Products Social Molecular Networking MolNetEnhancer workflow provided a more comprehensive understanding of the metabolic profiles. The results revealed the existence of a wide range of metabolites, however more than half of the compounds could not be identified. It was further observed that the metabolic diversity among the strains varied primarily due to the cultivation medium used. Together the results obtained here revealed the pharmacological potential of the bacteria isolated from Aplysina species.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"117-136"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142944239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2025-01-10DOI: 10.1007/s42770-024-01596-4
Gabriela B Caldas-Garcia, Ícaro Santos Lopes, Eric Roberto Guimarães Rocha Aguiar
Parasitoid wasps act as natural biological control agents for several harmful insect species. However, there is a lack of information regarding the exogenous RNA viruses that infect parasitoids and may contribute to the success of their parasitism strategies. This study aimed to investigate the presence, abundance, and replication of known exogenous viruses in two parasitoid wasp species and their corresponding preys. Utilizing publicly available RNA deep-sequencing data, two previously validated viruses from the parasitoid Tetrastichus brontispae were assessed in the target beetles Brontispa longissima and Octodonta nipae from the same geographic region. This study revealed the presence of the iflavirus TbRV-3 in both T. brontispae and O. nipae-derived samples, suggesting a potential exchange of the virus between the parasitoid and its host. In addition, there is substantial evidence that the Halyomorpha halys virus infects the parasitoid Telenomus podisi. Thus, this study proposes a close evolutionary relationship between the HhV strain identified in the parasitoid Telenomus podisi and the original strain detected in the prey H. halys. The viral association between trophically related species, such as parasitoids and their hosts, is demonstrated using features such as abundance and the presence of double-stranded RNA, which serves as a proxy for virus replication. Therefore, RNA viruses may coexist at both trophic levels, conferring an evolutionary advantage to the parasitism strategy.
{"title":"Expanding the evidence for cross-species viral transmission from trophic interactions of parasitoid wasps and their hosts.","authors":"Gabriela B Caldas-Garcia, Ícaro Santos Lopes, Eric Roberto Guimarães Rocha Aguiar","doi":"10.1007/s42770-024-01596-4","DOIUrl":"10.1007/s42770-024-01596-4","url":null,"abstract":"<p><p>Parasitoid wasps act as natural biological control agents for several harmful insect species. However, there is a lack of information regarding the exogenous RNA viruses that infect parasitoids and may contribute to the success of their parasitism strategies. This study aimed to investigate the presence, abundance, and replication of known exogenous viruses in two parasitoid wasp species and their corresponding preys. Utilizing publicly available RNA deep-sequencing data, two previously validated viruses from the parasitoid Tetrastichus brontispae were assessed in the target beetles Brontispa longissima and Octodonta nipae from the same geographic region. This study revealed the presence of the iflavirus TbRV-3 in both T. brontispae and O. nipae-derived samples, suggesting a potential exchange of the virus between the parasitoid and its host. In addition, there is substantial evidence that the Halyomorpha halys virus infects the parasitoid Telenomus podisi. Thus, this study proposes a close evolutionary relationship between the HhV strain identified in the parasitoid Telenomus podisi and the original strain detected in the prey H. halys. The viral association between trophically related species, such as parasitoids and their hosts, is demonstrated using features such as abundance and the presence of double-stranded RNA, which serves as a proxy for virus replication. Therefore, RNA viruses may coexist at both trophic levels, conferring an evolutionary advantage to the parasitism strategy.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"191-202"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142944493","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-11-06DOI: 10.1007/s42770-024-01552-2
Emiliane Fernanda Silva Freitas, Lucas Dutra Pinto Nunes, Jaqueline Aparecida de Oliveira, Olinto Liparini Pereira
Widely produced and marketed worldwide, orchids suffers from several diseases that have a negative effect on production. Black rot disease is among the most common and severe disease, characterized by black spots of rot on leaves, pseudobulbs and roots, which usually lead to the plant death. The world literature lists some Phytophthora species as causal agents of the disease, but there is no advanced study on the etiology of this disease in Brazil, which makes it difficult to determine an efficient control method. This work aims to contribute to the study of the etiology of black rot on Cattleya leopoldii in Brazil. Severely diseased C. leopoldii plants with typical symptoms of black rot, collected from a commercial orchid farm in Brazil, were taken to the laboratory and used to isolate the pathogen. Based on morphological characters analysis combined with molecular data, the isolates were identified as belonging to the species Phytophthora heterospora. This is the first worldwide report of P. heterospora causing black rot disease on orchids.
兰花在世界各地广泛生产和销售,但有几种病害会对生产造成负面影响。黑腐病是最常见、最严重的病害之一,其特征是叶片、假鳞茎和根部出现黑色腐烂斑点,通常会导致植株死亡。世界文献将一些疫霉菌列为黑腐病的病原菌,但巴西尚未对黑腐病的病因进行深入研究,因此难以确定有效的控制方法。这项工作旨在为巴西 Cattleya leopoldii 黑腐病的病原学研究做出贡献。从巴西的一个商业兰花农场收集到的具有典型黑腐病症状的重病 C. leopoldii 植株被送往实验室用于分离病原体。根据形态特征分析和分子数据,确定分离物属于异孢噬菌体(Phytophthora heterospora)。这是全世界首次报道异孢疫霉(P. heterospora)引起兰花黑腐病。
{"title":"Phytophthora heterospora is the causal agent of black rot disease on the orchid Cattleya leopoldii in Brazil.","authors":"Emiliane Fernanda Silva Freitas, Lucas Dutra Pinto Nunes, Jaqueline Aparecida de Oliveira, Olinto Liparini Pereira","doi":"10.1007/s42770-024-01552-2","DOIUrl":"10.1007/s42770-024-01552-2","url":null,"abstract":"<p><p>Widely produced and marketed worldwide, orchids suffers from several diseases that have a negative effect on production. Black rot disease is among the most common and severe disease, characterized by black spots of rot on leaves, pseudobulbs and roots, which usually lead to the plant death. The world literature lists some Phytophthora species as causal agents of the disease, but there is no advanced study on the etiology of this disease in Brazil, which makes it difficult to determine an efficient control method. This work aims to contribute to the study of the etiology of black rot on Cattleya leopoldii in Brazil. Severely diseased C. leopoldii plants with typical symptoms of black rot, collected from a commercial orchid farm in Brazil, were taken to the laboratory and used to isolate the pathogen. Based on morphological characters analysis combined with molecular data, the isolates were identified as belonging to the species Phytophthora heterospora. This is the first worldwide report of P. heterospora causing black rot disease on orchids.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"635-641"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142581851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-12-12DOI: 10.1007/s42770-024-01585-7
Evandro Ademir Deak, Thomas Newton Martin, Jessica Deolinda Leivas Stecca, Gerusa Mussuquini Conceição, Matheus Martins Ferreira, Vítor Sauzem Rumpel, Acir Felipe Grolli Carvalho, Francisco Javier López Baena
The success of biological nitrogen fixation (BNF) in soybean depends on two crucial factors, viz., seed inoculation and soil nutritional balance. The macronutrient sulfur (S) is vital to the formation of ferredoxin, a common source of electrons that controls the proper functioning of the subunits of the enzyme nitrogenase, responsible for the conversion of atmospheric nitrogen (N2) to ammonia (NH3+). However, as the S dynamics is a complex process in soil, it may cause to the plants to be sulfur limited. This study aims at assessing the relationship between S fertilization through the use of elemental-S, and bacterial inoculation (Bradyrhizobium spp.) and co-inoculation (Bradyrhizobium spp. and Azospirillum brasilense) on nodulation, production and quality of soybean. The study was performed on the 2017/2018 and 2018/2019 crop seasons, involving four experiments where two were carried out in Santa Maria and two in Augusto Pestana, Rio Grande do Sul, Brazil. Adopting the randomized experimental block design, the treatments included a 3 × 4 factorial design, with three inoculations (Non-inoculated control, Inoculation and Co-inoculation) together with four doses of S (0, 20, 40 and 60 kg ha- 1). Evaluations were done of the plant nodulation, accumulation of shoot dry matter, yield constituents, and quality of the soybean grain. S fertilization and co-inoculation promote an increase in plant nodulation, proving to be an important strategy to support nitrogen supply to soybean crops. The application of elemental sulfur in doses between 20 and 40 kg ha- 1 promotes nodulation, the accumulation of dry mass of plants, the productivity and quality of soybeans, in addition to benefiting nodulation when combined with co-inoculation of Bradyrhizobium ssp. and Azospirillum brasilense.
大豆生物固氮的成功与否取决于两个关键因素,即种子接种和土壤营养平衡。常量营养素硫(S)对铁氧还蛋白的形成至关重要,铁氧还蛋白是控制酶氮酶亚基正常功能的常见电子来源,负责将大气中的氮(N2)转化为氨(NH3+)。然而,由于土壤中硫的动态是一个复杂的过程,它可能会导致植物受到硫的限制。本研究旨在探讨元素硫施肥与细菌接种(慢生根瘤菌)和共接种(慢生根瘤菌与巴西氮螺旋菌)对大豆结瘤、产量和品质的关系。该研究在2017/2018和2018/2019作物季节进行,涉及四项实验,其中两项在圣玛丽亚进行,两项在巴西南大德州奥古斯托佩斯塔纳进行。试验采用随机区组设计,采用3 × 4因子设计,3次接种(未接种对照、接种和共接种),4次接种S(0、20、40和60 kg ha- 1)。对大豆植株结瘤、地上部干物质积累、产量成分和籽粒品质进行了评价。施硫和共接种促进了植物结瘤的增加,是支持大豆作物氮素供应的重要策略。单质硫的施用剂量在20 - 40 kg / h1之间,可促进结瘤、植物干质量的积累、大豆的产量和质量,此外,与缓生根瘤菌共接种也有利于结瘤。和巴西偶氮螺旋菌。
{"title":"Sulfur fertilization and inoculation of soybean with Azospirillum brasilense and Bradyrhizobium spp. can improve grain yield and quality.","authors":"Evandro Ademir Deak, Thomas Newton Martin, Jessica Deolinda Leivas Stecca, Gerusa Mussuquini Conceição, Matheus Martins Ferreira, Vítor Sauzem Rumpel, Acir Felipe Grolli Carvalho, Francisco Javier López Baena","doi":"10.1007/s42770-024-01585-7","DOIUrl":"10.1007/s42770-024-01585-7","url":null,"abstract":"<p><p>The success of biological nitrogen fixation (BNF) in soybean depends on two crucial factors, viz., seed inoculation and soil nutritional balance. The macronutrient sulfur (S) is vital to the formation of ferredoxin, a common source of electrons that controls the proper functioning of the subunits of the enzyme nitrogenase, responsible for the conversion of atmospheric nitrogen (N<sub>2</sub>) to ammonia (NH<sub>3</sub><sup>+</sup>). However, as the S dynamics is a complex process in soil, it may cause to the plants to be sulfur limited. This study aims at assessing the relationship between S fertilization through the use of elemental-S, and bacterial inoculation (Bradyrhizobium spp.) and co-inoculation (Bradyrhizobium spp. and Azospirillum brasilense) on nodulation, production and quality of soybean. The study was performed on the 2017/2018 and 2018/2019 crop seasons, involving four experiments where two were carried out in Santa Maria and two in Augusto Pestana, Rio Grande do Sul, Brazil. Adopting the randomized experimental block design, the treatments included a 3 × 4 factorial design, with three inoculations (Non-inoculated control, Inoculation and Co-inoculation) together with four doses of S (0, 20, 40 and 60 kg ha<sup>- 1</sup>). Evaluations were done of the plant nodulation, accumulation of shoot dry matter, yield constituents, and quality of the soybean grain. S fertilization and co-inoculation promote an increase in plant nodulation, proving to be an important strategy to support nitrogen supply to soybean crops. The application of elemental sulfur in doses between 20 and 40 kg ha<sup>- 1</sup> promotes nodulation, the accumulation of dry mass of plants, the productivity and quality of soybeans, in addition to benefiting nodulation when combined with co-inoculation of Bradyrhizobium ssp. and Azospirillum brasilense.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"573-588"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142811844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2025-01-15DOI: 10.1007/s42770-025-01612-1
Rachel Menezes Castelo, Marília de Albuquerque Oliveira, Roselayne Ferro Furtado, Bruno Peixoto de Oliveira, Lucas Vinicius Leite Martoni, Terezinha Feitosa Machado, Celli Rodrigues Muniz, Flávia Oliveira Monteiro da Silva Abreu, Sérgio Antônio Spinola Machado, Airis Maria Araújo Melo, Huai N Cheng, Atanu Biswas, Carlucio Roberto Alves
Carbon dots in biosensing have advanced significantly, adding improvements to different detection techniques. In this study, an amperometric immunosensor for Salmonella Thyphimurium was designed using antibodies labeled with carbon dots (Cdots) from pequi almond (Caryocar brasiliensis). Cdots were synthesized by pyrolysis and characterized by FTIR, UV/fluorescence, electrochemistry, zeta potential, and transmission electron microscopy (TEM). A particle size of 6.80 ± 2.13 nm was estimated, and the zeta potential was - 47.4 mV, indicating the preponderant presence of acidic groups, as confirmed by FTIR. The impedance evaluation of the response of biosensors assembled for live (Rct = 13.4 kΩ) and dead (Rct = 499.7 Ω) Salmonella showed a significant difference in their values, in agreement with chronoamperometric analyses, which had their current values drastically reduced from - 2.2 mA (live) to 0 mA (dead). An analytical curve for Salmonella was established with the limit of detection lower than 1 CFU/mL. This electrochemical biosensor using pequi carbon dots for antibody labeling showed promising results for detecting the pathogen. Thus, carbon dots can be used as substitutes for enzymes in labeling antibodies used in the design and production of sensors.
{"title":"Carbon-dot pequi-nut in the development of immunosensor to detect pathogenic bacteria.","authors":"Rachel Menezes Castelo, Marília de Albuquerque Oliveira, Roselayne Ferro Furtado, Bruno Peixoto de Oliveira, Lucas Vinicius Leite Martoni, Terezinha Feitosa Machado, Celli Rodrigues Muniz, Flávia Oliveira Monteiro da Silva Abreu, Sérgio Antônio Spinola Machado, Airis Maria Araújo Melo, Huai N Cheng, Atanu Biswas, Carlucio Roberto Alves","doi":"10.1007/s42770-025-01612-1","DOIUrl":"10.1007/s42770-025-01612-1","url":null,"abstract":"<p><p>Carbon dots in biosensing have advanced significantly, adding improvements to different detection techniques. In this study, an amperometric immunosensor for Salmonella Thyphimurium was designed using antibodies labeled with carbon dots (Cdots) from pequi almond (Caryocar brasiliensis). Cdots were synthesized by pyrolysis and characterized by FTIR, UV/fluorescence, electrochemistry, zeta potential, and transmission electron microscopy (TEM). A particle size of 6.80 ± 2.13 nm was estimated, and the zeta potential was - 47.4 mV, indicating the preponderant presence of acidic groups, as confirmed by FTIR. The impedance evaluation of the response of biosensors assembled for live (Rct = 13.4 kΩ) and dead (Rct = 499.7 Ω) Salmonella showed a significant difference in their values, in agreement with chronoamperometric analyses, which had their current values drastically reduced from - 2.2 mA (live) to 0 mA (dead). An analytical curve for Salmonella was established with the limit of detection lower than 1 CFU/mL. This electrochemical biosensor using pequi carbon dots for antibody labeling showed promising results for detecting the pathogen. Thus, carbon dots can be used as substitutes for enzymes in labeling antibodies used in the design and production of sensors.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"275-284"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142982756","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-12-02DOI: 10.1007/s42770-024-01575-9
Yangjing Ou, Dan Li, Xi Long, Huiyang He, Ling Qing, Yuqiu Tian, Jing Ren, Qing Zhou, Yingzheng Tan
The objective of this study was to investigate the early diagnostic value of nanopore sequencing in alveolar lavage smear-negative pulmonary tuberculosis (PTB). A prospective study was conducted on patients hospitalized at Zhuzhou Central Hospital from October 2021 to June 2022 and suspected to have PTB. Alveolar lavage fluid specimens were collected from these patients and simultaneously subjected to centrifugal bacterial collection smear method in a sandwich cup, bifidobacteria solid culture (referred to as culture), Mycobacterium tuberculosis-DNA (TB-DNA), and nanopore sequencing for detection of Mycobacterium tuberculosis. These patients were ultimately diagnosed with smear-negative PTB. The final clinical diagnosis was used as a reference to compare the diagnostic efficacy of Nanopore sequencing, culture, and TB-DNA for PTB. The results showed that the positive rates detected by nanopore sequencing, culture, and TB-DNA in the 103 suspected tuberculosis patients were 73.8%, 13.6%, and 33.0%, respectively. The sensitivity of nanopore sequencing was significantly higher than culture (P < 0.001) and TB-DNA (P < 0.001) for the identification of smear-negative PTB. Similarly, the positive rate of TB-DNA was also significantly higher than that of culture (P = 0.001). In conclusion, nanopore sequencing exhibited the highest sensitivity for the rapid diagnosis of Mycobacterium tuberculosis in alveolar lavage fluid specimens, using clinical diagnosis as a reference standard, and it could improve the PTB clinical diagnosis.
本研究的目的是探讨纳米孔测序在肺泡灌洗涂片阴性肺结核(PTB)中的早期诊断价值。对2021年10月至2022年6月在株洲中心医院住院的疑似肺结核患者进行前瞻性研究。采集患者肺泡灌洗液标本,同时采用夹心杯离心细菌收集涂片法、双歧杆菌固体培养(简称培养)、结核分枝杆菌- dna (TB-DNA)、纳米孔测序检测结核分枝杆菌。这些患者最终被诊断为涂片阴性肺结核。以最终的临床诊断为参考,比较纳米孔测序、培养和TB-DNA对PTB的诊断效果。结果表明,103例疑似结核患者的纳米孔测序、培养和TB-DNA阳性率分别为73.8%、13.6%和33.0%。纳米孔测序的灵敏度显著高于培养(P
{"title":"Study on the early diagnostic value of nanopore sequencing in alveolar lavage fluid smear-negative pulmonary tuberculosis.","authors":"Yangjing Ou, Dan Li, Xi Long, Huiyang He, Ling Qing, Yuqiu Tian, Jing Ren, Qing Zhou, Yingzheng Tan","doi":"10.1007/s42770-024-01575-9","DOIUrl":"10.1007/s42770-024-01575-9","url":null,"abstract":"<p><p>The objective of this study was to investigate the early diagnostic value of nanopore sequencing in alveolar lavage smear-negative pulmonary tuberculosis (PTB). A prospective study was conducted on patients hospitalized at Zhuzhou Central Hospital from October 2021 to June 2022 and suspected to have PTB. Alveolar lavage fluid specimens were collected from these patients and simultaneously subjected to centrifugal bacterial collection smear method in a sandwich cup, bifidobacteria solid culture (referred to as culture), Mycobacterium tuberculosis-DNA (TB-DNA), and nanopore sequencing for detection of Mycobacterium tuberculosis. These patients were ultimately diagnosed with smear-negative PTB. The final clinical diagnosis was used as a reference to compare the diagnostic efficacy of Nanopore sequencing, culture, and TB-DNA for PTB. The results showed that the positive rates detected by nanopore sequencing, culture, and TB-DNA in the 103 suspected tuberculosis patients were 73.8%, 13.6%, and 33.0%, respectively. The sensitivity of nanopore sequencing was significantly higher than culture (P < 0.001) and TB-DNA (P < 0.001) for the identification of smear-negative PTB. Similarly, the positive rate of TB-DNA was also significantly higher than that of culture (P = 0.001). In conclusion, nanopore sequencing exhibited the highest sensitivity for the rapid diagnosis of Mycobacterium tuberculosis in alveolar lavage fluid specimens, using clinical diagnosis as a reference standard, and it could improve the PTB clinical diagnosis.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"365-372"},"PeriodicalIF":2.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142766171","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}