Frontiers in Cellular and Infection Microbiology最新文献

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CATH-2-derived antimicrobial peptide inhibits multidrug-resistant Escherichia coli infection in chickens 源自 CATH-2 的抗菌肽可抑制鸡感染耐多药大肠杆菌
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-05-15 DOI: 10.3389/fcimb.2024.1390934
Shihao Hao, Wenhui Shi, Liujun Chen, Tianyou Kong, Bin Wang, Shuming Chen, Xiaomin Guo
{"title":"CATH-2-derived antimicrobial peptide inhibits multidrug-resistant Escherichia coli infection in chickens","authors":"Shihao Hao, Wenhui Shi, Liujun Chen, Tianyou Kong, Bin Wang, Shuming Chen, Xiaomin Guo","doi":"10.3389/fcimb.2024.1390934","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1390934","url":null,"abstract":"Avian colibacillosis (AC), caused by infection with Escherichia coli (E. coli), is a major threat to poultry health, food safety and public health, and results in high mortality and significant economic losses. Currently, new drugs are urgently needed to replace antibiotics due to the continuous emergence and increasing resistance of multidrug-resistant (MDR) strains of E. coli caused by the irrational use of antibiotics in agriculture and animal husbandry. In recent years, antimicrobial peptides (AMPs), which uniquely evolved to protect the host, have emerged as a leading alternative to antibiotics in clinical settings. CATH-2, a member of the antimicrobial cathelicidin peptide family, has been reported to have antibacterial activity. To enhance the antimicrobial potency and reduce the adverse effects on animals, we designed five novel AMPs, named C2-1, C2-2, C2-3, C2-4 and C2-5, based on chicken CATH-2, the secondary structures of these AMPs were consistently α-helical and had an altered net charge and hydrophobicity compared to those of the CATH-2 (1-15) sequences. Subsequently, the antimicrobial activities of CATH-2 (1-15) and five designed peptides against MDR E. coli were evaluated in vitro. Specifically, C2-2 showed excellent antimicrobial activity against either the ATCC standard strain or veterinary clinical isolates of MDR E. coli, with concentrations ranging from 2-8 μg/mL. Furthermore, C2-2 maintained its strong antibacterial efficacy under high temperature and saline conditions, demonstrating significant stability. Similarly, C2-2 retained a high level of safety with no significant hemolytic activity on chicken mature red blood cells or cytotoxicity on chicken kidney cells over the concentration range of 0-64 μg/mL. Moreover, the administration of C2-2 improved the survival rate and reduced the bacterial load in the heart, liver and spleen during MDR E. coli infection in chickens. Additionally, pathological damage to the heart, liver and intestine was prevented when MDR E. coli infected chickens were treated with C2-2. Together, our study showed that C2-2 may be a promising novel therapeutic agent for the treatment of MDR E. coli infections and AC.","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"63 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140973626","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Structural and functional alteration of the gut microbiota in elderly patients with hyperlipidemia 老年高脂血症患者肠道微生物群的结构和功能改变
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-05-15 DOI: 10.3389/fcimb.2024.1333145
Meng Xia, Yafang Xu, Huajun Li, Juan Huang, Haolin Zhou, Chuanzhou Gao, Jingyi Han
{"title":"Structural and functional alteration of the gut microbiota in elderly patients with hyperlipidemia","authors":"Meng Xia, Yafang Xu, Huajun Li, Juan Huang, Haolin Zhou, Chuanzhou Gao, Jingyi Han","doi":"10.3389/fcimb.2024.1333145","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1333145","url":null,"abstract":"To investigate the structure, composition, and functions of the gut microbiota in elderly patients with hyperlipidemia.Sixteen older patients diagnosed with hyperlipidemia (M group) and 10 healthy, age-matched normal volunteers (N group) were included. These groups were further subdivided by sex into the male normal (NM, n = 5), female normal (NF, n = 5), male hyperlipidemia (MM, n = 8), and female hyperlipidemia (MF, n = 8) subgroups. Stool samples were collected for high-throughput sequencing of 16S rRNA genes. Blood samples were collected for clinical biochemical index testing.Alpha- and beta-diversity analyses revealed that the structure and composition of the gut microbiota were significantly different between the M and N groups. The relative abundances of Bacteroides, Parabacteroides, Blautia, Peptococcus, and Bifidobacterium were significantly decreased, while those of Lactobacillus, Helicobacter, and Desulfovibrio were significantly higher in the M group. There were also significant sex-related differences in microbial structure between the NM and NF groups, and between the MM and MF groups. Through functional prediction with PICRUSt 2, we observed distinct between-group variations in metabolic pathways associated with the gut microbiota and their impact on the functionality of the nervous system. Pearson’s correlation coefficient was used as a distance metric to build co-abundance networks. A hypergeometric test was used to detect taxonomies with significant enrichment in specific clusters. We speculated that modules with Muribaculaceae and Lachnospiraceae as the core microbes play an important ecological role in the intestinal microbiota of the M group. The relative intestinal abundances of Agathobacter and Faecalibacterium in the M group were positively correlated with serum triglyceride and low-density lipoprotein levels, while the relative abundance of Bifidobacterium was negatively correlated with the serum lipoprotein a level.","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"72 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140973587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Small non-coding RNAs in Gram negative bacteria 社论:革兰氏阴性细菌中的小非编码 RNA
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-05-13 DOI: 10.3389/fcimb.2024.1426124
Bindu Subhadra, M. Sarshar
{"title":"Editorial: Small non-coding RNAs in Gram negative bacteria","authors":"Bindu Subhadra, M. Sarshar","doi":"10.3389/fcimb.2024.1426124","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1426124","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"05 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140984259","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Stem cell technologies meet stem cell biology to shine new light into tropical infectious diseases 社论:干细胞技术与干细胞生物学相结合,为热带传染病带来新曙光
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-05-07 DOI: 10.3389/fcimb.2024.1411728
Alena Pance, Gabriel Rinaldi
{"title":"Editorial: Stem cell technologies meet stem cell biology to shine new light into tropical infectious diseases","authors":"Alena Pance, Gabriel Rinaldi","doi":"10.3389/fcimb.2024.1411728","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1411728","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"67 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141002367","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: COVID-19 and vaccination-associated ocular complications 社论:COVID-19 和疫苗接种相关眼部并发症
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-05-06 DOI: 10.3389/fcimb.2024.1413435
Xinyuan Zhang, Rachael Niederer, Kelvin Yi Chong Teo
{"title":"Editorial: COVID-19 and vaccination-associated ocular complications","authors":"Xinyuan Zhang, Rachael Niederer, Kelvin Yi Chong Teo","doi":"10.3389/fcimb.2024.1413435","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1413435","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"161 8‐10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141007224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Standards in personalized phage therapy: from phage collection to phage production 社论:个性化噬菌体疗法的标准:从噬菌体采集到噬菌体生产
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-03-22 DOI: 10.3389/fcimb.2024.1376386
S. Kiljunen, Grégory Resch
{"title":"Editorial: Standards in personalized phage therapy: from phage collection to phage production","authors":"S. Kiljunen, Grégory Resch","doi":"10.3389/fcimb.2024.1376386","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1376386","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":" 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140219304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A multicenter clinical epidemiology of pediatric pneumococcal meningitis in China: results from the Chinese Pediatric Bacterial Meningitis Surveillance (CPBMS) 2019–2020 中国小儿肺炎球菌脑膜炎多中心临床流行病学:2019-2020年中国小儿细菌性脑膜炎监测(CPBMS)结果
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-03-15 DOI: 10.3389/fcimb.2024.1353433
Caiyun Wang, Hongmei Xu, Gang Liu, Jing Liu, Hui Yu, Biquan Chen, Guo Zheng, Min Shu, Lijun Du, Zhiwei Xu, Lisu Huang, Haibo Li, Sainan Shu, Ying-Hu Chen
{"title":"A multicenter clinical epidemiology of pediatric pneumococcal meningitis in China: results from the Chinese Pediatric Bacterial Meningitis Surveillance (CPBMS) 2019–2020","authors":"Caiyun Wang, Hongmei Xu, Gang Liu, Jing Liu, Hui Yu, Biquan Chen, Guo Zheng, Min Shu, Lijun Du, Zhiwei Xu, Lisu Huang, Haibo Li, Sainan Shu, Ying-Hu Chen","doi":"10.3389/fcimb.2024.1353433","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1353433","url":null,"abstract":"To analyze the clinical epidemiological characteristics including clinical features, disease prognosis of pneumococcal meningitis (PM), and drug sensitivity of S. pneumoniae isolates in Chinese children.A retrospective analysis was performed on the clinical, laboratory microbiological data of 160 hospitalized children less than 15 years of age with PM from January 2019 to December 2020 in 33 tertiary hospitals in China.A total of 160 PM patients were diagnosed, including 103 males and 57 females The onset age was 15 days to 15 years old, and the median age was 1 year and 3 months. There were 137 cases (85.6%) in the 3 months to <5 years age group, especially in the 3 months to <3 years age group (109 cases, 68.2%); S. pneumoniae was isolated from cerebrospinal fluid (CSF) culture in 95(35.6%), and 57(35.6%) in blood culture. The positive rates of S. pneumoniae detection by CSF metagenomic next-generation sequencing (mNGS)and antigen detection method were 40.2% (35/87) and 26.9% (21/78). Fifty-five cases (34.4%) had one or more predisposing factors of bacterial meningitis; and 113 cases (70.6%) had one or more extracranial infection diseases Fever (147, 91.9%) was the most common clinical symptom, followed by vomiting (61, 38.1%) and altered mental status (47,29.4%). Among 160 children with PM, the main intracranial imaging complications were subdural effusion and (or) empyema in 43 cases (26.9%), hydrocephalus in 24 cases (15.0%), cerebral abscess in 23 cases (14.4%), intracranial hemorrhage in 8 cases (5.0%), and other cerebrovascular diseases in 13 cases (8.1%) including encephalomalacia, cerebral infarction, and encephalatrophy. Subdural effusion and (or) empyema and hydrocephalus mainly occurred in children < 1 years old (90.7% (39/43) and 83.3% (20/24), respectively). 17 cases with PM (39.5%) had more than one intracranial imaging abnormality. S. pneumoniae isolates were completely sensitive to vancomycin (100.0%, 75/75), linezolid (100.0%,56/56), ertapenem (6/6); highly sensitive to levofloxacin (81.5%, 22/27), moxifloxacin (14/17), rifampicin (96.2%, 25/26), and chloramphenicol (91.3%, 21/23); moderately sensitive to cefotaxime (56.1%, 23/41), meropenem (51.1%, 23/45) and ceftriaxone (63.5, 33/52); less sensitive to penicillin (19.6%, 27/138) and clindamycin (1/19); completely resistant to erythromycin (100.0%, 31/31). The cure and improvement rate were 22.5% (36/160)and 66.3% (106/160), respectively. 18 cases (11.3%) had an adverse outcome, including 6 cases withdrawing treatment therapy, 5 cases unhealed, 5 cases died, and 2 recurrences. S. pneumoniae was completely susceptible to vancomycin (100.0%, 75/75), linezolid (100.0%, 56/56), and ertapenem (6/6); susceptible to cefotaxime, meropenem, and ceftriaxone in the order of 56.1% (23/41), 51.1% (23/45), and 63.5 (33/52); completely resistant to erythromycin (100.0%, 31/31).Pediatric PM is more common in children aged 3 months to < 3 years old. Intracranial complications mostly occur in c","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"77 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140239572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Combating antimicrobial resistance: peptides and other novel therapeutic interventions to treat ocular, oral and skin infections 社论:对抗抗菌药耐药性:治疗眼部、口腔和皮肤感染的肽和其他新型治疗干预措施
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-03-14 DOI: 10.3389/fcimb.2024.1388744
Sanhita Roy, Peter N. Monk
{"title":"Editorial: Combating antimicrobial resistance: peptides and other novel therapeutic interventions to treat ocular, oral and skin infections","authors":"Sanhita Roy, Peter N. Monk","doi":"10.3389/fcimb.2024.1388744","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1388744","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"8 16","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140242115","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Prophylactic efficacy and safety of COVID-19 vaccines in preventing disease caused by various SARS CoV-2 variants 社论:COVID-19疫苗预防各种SARS CoV-2变种引起的疾病的有效性和安全性
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-03-13 DOI: 10.3389/fcimb.2024.1384601
Haidar Abdul-Lateef Mousa, M. A. Ansari
{"title":"Editorial: Prophylactic efficacy and safety of COVID-19 vaccines in preventing disease caused by various SARS CoV-2 variants","authors":"Haidar Abdul-Lateef Mousa, M. A. Ansari","doi":"10.3389/fcimb.2024.1384601","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1384601","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"1990 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140246652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Strategies in the drug discovery and development for leishmaniasis: immunomodulators, natural products, synthetic compounds, and drug repositioning 社论:利什曼病药物研发战略:免疫调节剂、天然产品、合成化合物和药物重新定位
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-03-13 DOI: 10.3389/fcimb.2024.1384244
Taís Fontoura de Almeida, Edézio F. Cunha-Junior, João Luiz Mendes Wanderley, Juliana da Silva Pacheco, L. H. Pinto-da-Silva, V. V. Andrade-Neto, Suzana Passos Chaves
{"title":"Editorial: Strategies in the drug discovery and development for leishmaniasis: immunomodulators, natural products, synthetic compounds, and drug repositioning","authors":"Taís Fontoura de Almeida, Edézio F. Cunha-Junior, João Luiz Mendes Wanderley, Juliana da Silva Pacheco, L. H. Pinto-da-Silva, V. V. Andrade-Neto, Suzana Passos Chaves","doi":"10.3389/fcimb.2024.1384244","DOIUrl":"https://doi.org/10.3389/fcimb.2024.1384244","url":null,"abstract":"","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140245840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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