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Identification of avaC from Human Gut Microbial Isolates that Converts 5AVA to 2-Piperidone
Qiudi Zhou, Lihui Feng
J. Microbiol. 2024;62(5):367-379.   Published online June 17, 2024
DOI: https://doi.org/10.1007/s12275-024-00141-0
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AbstractAbstract
2-piperidone is a crucial industrial raw material of high-value nylon-5 and nylon-6,5. Currently, a major bottleneck in the biosynthesis of 2-piperidone is the identification of highly efficient 2-piperidone synthases. In this study, we aimed to identify specific strains among 51 human gut bacterial strains capable of producing 2-piperidone and to elucidate its synthetic mechanism. Our findings revealed that four gut bacterial strains, namely Collinsella aerofaciens LFYP39, Collinsella intestinalis LFYP54, Clostridium bolteae LFYP116, and Clostridium hathewayi LFYP18, could produce 2-piperidone from 5-aminovaleric acid (5AVA). Additionally, we observed that 2-piperidone could be synthesized from proline through cross-feeding between Clostridium difficile LFYP43 and one of the four 2-piperidone producing strains, respectively. To identify the enzyme responsible for catalyzing the conversion of 5AVA to 2-piperidone, we utilized a gain-of-function library and identified avaC (5-aminovaleric acid cyclase) in C. intestinalis LFYP54. Moreover, homologous genes of avaC were validated in the other three bacterial strains. Notably, avaC were found to be widely distributed among environmental bacteria. Overall, our research delineated the gut bacterial strains and genes involved in 2-piperidone production, holding promise for enhancing the efficiency of industrial biosynthesis of this compound.
Review
[Minireview]The rationale and potential for using Lactobacillus in the management of periodontitis
Jiaqi Wang , Yingman Liu , Weiru Wang , Jiaojiao Ma , Manman Zhang , Xiaoying Lu , Jie Liu , Yurong Kou
J. Microbiol. 2022;60(4):355-363.   Published online March 28, 2022
DOI: https://doi.org/10.1007/s12275-022-1514-4
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  • 12 Crossref
AbstractAbstract
Periodontitis refers to a wide range of the inflammatory conditions of supporting dental structures. For some patients with periodontitis, antibacterial agents are needed as an adjuvant to mechanical debridement treatments and oral hygiene maintenance. However, the widespread use of broad-spectrum antibiotics for the prophylaxis and treatment of periodontal infections
results
in the emergence of resistant pathogens. Therefore, probiotics have become markedly interesting to researchers as a potentially safe alternative to periodontal treatment and maintenance. Probiotics have been used in medicine for decades and extensively applied to the treatment of inflammatory diseases through the modulation of microbial synergy and other mechanisms. A growing amount of evidence has shown that using Lactobacillus strains for oral cavity maintenance could improve periodontal health. In this study, we reviewed studies showing proof of the inhibitory effects of Lactobacillus species on periodontal inflammation. We also explored the rationale and potential for using Lactobacillus species in the management of periodontitis.

Citations

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  • The Effectiveness of Probiotics on Oral Health During Adult Orthodontic Treatment With Fixed Appliances: A Two-Arm Parallel-Group Randomized Controlled Clinical Trial
    Lana Hasan Albardawel, Kinda Sultan, Mohammad Y. Hajeer, Mohammad Maarouf
    Cureus.2024;[Epub]     CrossRef
  • New insights into nanotherapeutics for periodontitis: a triple concerto of antimicrobial activity, immunomodulation and periodontium regeneration
    Jiaxin Li, Yuxiao Wang, Maomao Tang, Chengdong Zhang, Yachen Fei, Meng Li, Mengjie Li, Shuangying Gui, Jian Guo
    Journal of Nanobiotechnology.2024;[Epub]     CrossRef
  • HAMLET, a human milk protein-lipid complex, modulates amoxicillin induced changes in an ex vivo biofilm model of the oral microbiome
    Navdeep Kaur Brar, Achal Dhariwal, Sudhanshu Shekhar, Roger Junges, Anders P. Hakansson, Fernanda Cristina Petersen
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Limosilactobacillus reuteri supernatant attenuates inflammatory responses of human gingival fibroblasts to LPS but not to elevated glucose levels
    T. M. Janson, L. L. Ramenzoni, C. R. Hatz, U. Schlagenhauf, T. Attin, P. R. Schmidlin
    Journal of Periodontal Research.2024; 59(5): 974.     CrossRef
  • Microbiological and clinical effects of probiotic-related Zeger therapy on gingival health: a randomized controlled clinical trial
    Xin Chen, Yi Zhao, Kun Xue, Mengyao Leng, Wei Yin
    BMC Oral Health.2024;[Epub]     CrossRef
  • Mediterranean diet: a potential player in the link between oral microbiome and oral diseases
    Giuseppina Augimeri, Giovanna Caparello, Ippolito Caputo, Rodolfo Reda, Luca Testarelli, Daniela Bonofiglio
    Journal of Oral Microbiology.2024;[Epub]     CrossRef
  • Effect of Dietary Composite Probiotic Supplementation on the Microbiota of Different Oral Sites in Cats
    Mingrui Zhang, Yingyue Cui, Xiaoying Mei, Longxian Li, Haotian Wang, Yingying Li, Yi Wu
    Veterinary Sciences.2024; 11(8): 351.     CrossRef
  • Efficacy of the Probiotic L. brevis in Counteracting the Demineralizing Process of the Tooth Enamel Surface: Results from an In Vitro Study
    Serena Altamura, Francesca Rosaria Augello, Eleonora Ortu, Davide Pietropaoli, Benedetta Cinque, Mario Giannoni, Francesca Lombardi
    Biomolecules.2024; 14(5): 605.     CrossRef
  • Effects of systemic Bifidobacterium longum and Lactobacillus rhamnosus probiotics on the ligature-induced periodontitis in rat
    Ying-Wu Chen, Ming-Lun Lee, Cheng-Yang Chiang, Earl Fu
    Journal of Dental Sciences.2023; 18(4): 1477.     CrossRef
  • Evaluation of Antioxidant and Antibacterial Effects of Lyophilized Cell-Free Probiotic Supernatants of Three Lactobacillus spp. and Their Cytocompatibility Against Periodontal Ligament Stem Cells
    Maryam Torshabi, Mohammad Mahdi Bardouni, Atieh Hashemi
    Iranian Journal of Pharmaceutical Research.2023;[Epub]     CrossRef
  • Managing Oral Health in the Context of Antimicrobial Resistance
    Lucinda J. Bessa, João Botelho, Vanessa Machado, Ricardo Alves, José João Mendes
    International Journal of Environmental Research and Public Health.2022; 19(24): 16448.     CrossRef
  • Use of the Probiotic Bifidobacterium animalis subsp. lactis HN019 in Oral Diseases
    Lisa Danielly Curcino Araujo, Flávia Aparecida Chaves Furlaneto, Léa Assed Bezerra da Silva, Yvonne L. Kapila
    International Journal of Molecular Sciences.2022; 23(16): 9334.     CrossRef
Journal Articles
Genetic characterization of African swine fever virus in Cameroon, 2010–2018
Abel Wade , Jenna Elizabeth Achenbach , Carmina Gallardo , Tirumala Bharani K. Settypalli , Abdoulkadiri Souley , Gaston Djonwe , Angelika Loitsch , Gwenaelle Dauphin , Jean Justin Essia Ngang , Onana Boyomo , Giovanni Cattoli , Adama Diallo , Charles Euloge Lamien
J. Microbiol. 2019;57(4):316-324.   Published online March 30, 2019
DOI: https://doi.org/10.1007/s12275-019-8457-4
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AbstractAbstract
African swine fever (ASF) is a highly lethal haemorrhagic disease in domestic and wild swine that has acquired great importance in sub-Saharan Africa since 1997. ASF was first reported in Cameroon in 1982 and was detected only in Southern Cameroon (South, West, East, Northwest, Southwest, Littoral, and Centre regions) until February 2010 when suspected ASF outbreaks were reported in the North and Far North regions. We investigated those outbreaks by analysing samples that were collected from sick pigs between 2010 and 2018. We confirmed 428 positive samples by ELISA and realtime PCR and molecularly characterized 48 representative isolates. All the identified virus isolates were classified as ASFV genotype I based on the partial B646L gene (C-terminal end of VP72 gene) and the full E183L gene encoding p54 protein analysis. Furthermore, analysis of the central variable region (CVR) within the B602L gene demonstrated that there were 3 different variants of ASFV genotype I, with 19, 20, and 21 tetrameric tandem repeat sequences (TRSs), that were involved in the 2010–2018 outbreaks in Cameroon. Among them, only variant A (19 TRSs) was identical to the Cam/82 isolate found in the country during the first outbreaks in 1981–1982. This study demonstrated that the three variants of ASFV isolates involved in these outbreaks were similar to those of neighbouring countries, suggesting a movement of ASFV strains across borders. Designing common control measures in affected regions and providing a compensation programme for farmers will help reduce the incidence and spread of this disease.

Citations

Citations to this article as recorded by  
  • African swine fever; insights into genomic aspects, reservoirs and transmission patterns of virus
    Bader S. Alotaibi, Chia-Hung Wu, Majid Khan, Mohsin Nawaz, Chien-Chin Chen, Abid Ali
    Frontiers in Veterinary Science.2024;[Epub]     CrossRef
  • Assessment of Nine Real-Time PCR Kits for African Swine Fever Virus Approved in Republic of Korea
    Siwon Lee, Tae Uk Han, Jin-Ho Kim
    Viruses.2024; 16(10): 1627.     CrossRef
  • A multi gene-approach genotyping method identifies 24 genetic clusters within the genotype II-European African swine fever viruses circulating from 2007 to 2022
    Carmina Gallardo, Nadia Casado, Alejandro Soler, Igor Djadjovski, Laura Krivko, Encarnación Madueño, Raquel Nieto, Covadonga Perez, Alicia Simon, Emiliya Ivanova, Daniel Donescu, Vesna Milicevik, Eleni Chondrokouki, Imbi Nurmoja, Maciej Frant, Francesco F
    Frontiers in Veterinary Science.2023;[Epub]     CrossRef
  • Internal Validation of the ASFV MONODOSE dtec-qPCR Kit for African Swine Fever Virus Detection under the UNE-EN ISO/IEC 17025:2005 Criteria
    Gema Bru, Marta Martínez-Candela, Paloma Romero, Aaron Navarro, Antonio Martínez-Murcia
    Veterinary Sciences.2023; 10(9): 564.     CrossRef
  • Porcine circovirus‐2 in Africa: Identification of continent‐specific clusters and evidence of independent viral introductions from Europe, North America and Asia
    Giovanni Franzo, Tirumala B.K. Settypalli, Ebere Roseann Agusi, Clement Meseko, Germaine Minoungou, Bruno Lalidia Ouoba, Zerbo Lamouni Habibata, Abel Wade, José Luís de Barros, Curé Georges Tshilenge, Esayas Gelaye, Martha Yami, Daniel Gizaw, Tesfaye Rufa
    Transboundary and Emerging Diseases.2022;[Epub]     CrossRef
  • A QP509L/QP383R-Deleted African Swine Fever Virus Is Highly Attenuated in Swine but Does Not Confer Protection against Parental Virus Challenge
    Dan Li, Panxue Wu, Huanan Liu, Tao Feng, Wenping Yang, Yi Ru, Pan Li, Xiaolan Qi, Zhengwang Shi, Haixue Zheng, Tom Gallagher
    Journal of Virology.2022;[Epub]     CrossRef
  • Comparison of the sensitivity, specificity, correlation and inter‐assay agreement of eight diagnostic in vitro assays for the detection of African swine fever virus
    Agathe Auer, Tirumala B.K. Settypalli, Beatrice Mouille, Angelique Angot, Cristian De Battisti, Charles E. Lamien, Giovanni Cattoli
    Transboundary and Emerging Diseases.2022;[Epub]     CrossRef
  • Review of the Pig-Adapted African Swine Fever Viruses in and Outside Africa
    Mary-Louise Penrith, Juanita Van Heerden, Livio Heath, Edward Okoth Abworo, Armanda D. S. Bastos
    Pathogens.2022; 11(10): 1190.     CrossRef
  • Molecular characterization of African swine fever viruses from Burkina Faso, 2018
    Moctar Sidi, Habibata Lamouni Zerbo, Bruno Lalidia Ouoba, Tirumala Bharani K. Settypalli, Gregorie Bazimo, Hamidou Sandaogo Ouandaogo, Boubacar N’paton Sie, Ilboudo Sidwatta Guy, Drabo Dji-tombo Adama, Joseph Savadogo, Anne Kabore-Ouedraogo, Marietou Guit
    BMC Veterinary Research.2022;[Epub]     CrossRef
  • Functional Analysis and Proteomics Profiling of Extracellular Vesicles From Swine Plasma Infected by African Swine Fever Virus
    Guowei Xu, Xijuan Shi, Huanan Liu, Chaochao Shen, Bo Yang, Ting Zhang, Xuehui Chen, Dengshuai Zhao, Jinke Yang, Yu Hao, Huimei Cui, Xingguo Yuan, Xiangtao Liu, Keshan Zhang, Haixue Zheng
    Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
  • Molecular Characterization of African Swine Fever Virus From 2019-2020 Outbreaks in Guangxi Province, Southern China
    Kaichuang Shi, Huixin Liu, Yanwen Yin, Hongbin Si, Feng Long, Shuping Feng
    Frontiers in Veterinary Science.2022;[Epub]     CrossRef
  • Molecular Characterization of ASFV and Differential Diagnosis of Erysipelothrix in ASFV-Infected Pigs in Pig Production Regions in Cameroon
    Ebanja Joseph Ebwanga, Stephen Mbigha Ghogomu, Jan Paeshuyse
    Veterinary Sciences.2022; 9(8): 440.     CrossRef
  • Risk factors of African swine fever virus in suspected infected pigs in smallholder farming systems in South-Kivu province, Democratic Republic of Congo
    Patrick N. Bisimwa, Michel Dione, Bisimwa Basengere, Ciza Arsène Mushagalusa, Lucilla Steinaa, Juliette Ongus
    Journal of Veterinary Science.2021;[Epub]     CrossRef
  • Molecular characterization of African Swine fever viruses in Burkina Faso, Mali, and Senegal 1989–2016
    Germaine L. Minoungou, Mariame Diop, Marthin Dakouo, Abdoul Karim Ouattara, Tirumala Bharani K. Settypalli, Modou M. Lo, Satigui Sidibe, Estelle Kanyala, Yaya Sidi Kone, Moctar Sidi Diallo, Anne Ouedraogo, Kadiatou Coulibaly, Victorine Ouedraogo, Ibrahim
    Transboundary and Emerging Diseases.2021; 68(5): 2842.     CrossRef
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    Fengxue Wang, He Zhang, Lina Hou, Chao Yang, Yongjun Wen
    Research in Veterinary Science.2021; 136: 535.     CrossRef
  • African Swine Fever Virus (ASFV): Biology, Genomics and Genotypes Circulating in Sub-Saharan Africa
    Emma P. Njau, Eunice M. Machuka, Sarah Cleaveland, Gabriel M. Shirima, Lughano J. Kusiluka, Edward A. Okoth, Roger Pelle
    Viruses.2021; 13(11): 2285.     CrossRef
  • African Swine Fever in Cameroon: A Review
    Ebanja Joseph Ebwanga, Stephen Mbigha Ghogomu, Jan Paeshuyse
    Pathogens.2021; 10(4): 421.     CrossRef
  • African Swine Fever: Prevalence, Farm Characteristics, Farmer’s Insight and Attitude toward Reporting of African Swine Fever Cases in the Northwest, West, Littoral and Southwest Regions of Cameroon
    Ebanja Joseph Ebwanga, Stephen Mbigha Ghogomu, Jan Paeshuyse
    Agriculture.2021; 12(1): 44.     CrossRef
  • Isolation and Genetic Characterization of African Swine Fever Virus from Domestic Pig Farms in South Korea, 2019
    Hyun-Joo Kim, Ki-Hyun Cho, Ji-Hyoung Ryu, Min-Kyung Jang, Ha-Gyeong Chae, Ji-Da Choi, Jin-Ju Nah, Yong-Joo Kim, Hae-Eun Kang
    Viruses.2020; 12(11): 1237.     CrossRef
  • Genetic Analysis of African Swine Fever Virus From the 2018 Outbreak in South-Eastern Burundi
    Jean N. Hakizimana, Lionel Nyabongo, Jean B. Ntirandekura, Clara Yona, Désiré Ntakirutimana, Olivier Kamana, Hans Nauwynck, Gerald Misinzo
    Frontiers in Veterinary Science.2020;[Epub]     CrossRef
  • A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
    Lynnette C. Goatley, Ana Luisa Reis, Raquel Portugal, Hannah Goldswain, Gareth L. Shimmon, Zoe Hargreaves, Chak-Sum Ho, María Montoya, Pedro J. Sánchez-Cordón, Geraldine Taylor, Linda K. Dixon, Christopher L. Netherton
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  • Epidemiology of African Swine Fever in Piggeries in the Center, South and South-West of Cameroon
    Victor Ngu Ngwa, Abdelrazak Abouna, André Pagnah Zoli, Anna-Rita Attili
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  • A seven-gene-deleted African swine fever virus is safe and effective as a live attenuated vaccine in pigs
    Weiye Chen, Dongming Zhao, Xijun He, Renqiang Liu, Zilong Wang, Xianfeng Zhang, Fang Li, Dan Shan, Hefeng Chen, Jiwen Zhang, Lulu Wang, Zhiyuan Wen, Xijun Wang, Yuntao Guan, Jinxiong Liu, Zhigao Bu
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    Sandra Blome, Kati Franzke, Martin Beer
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  • Molecular Characterization of African Swine Fever Virus Isolates in Estonia in 2014–2019
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  • Molecular characterization of African swine fever virus from outbreaks in Namibia in 2018
    Umberto Molini, Borden Mushonga, Tirumala B. K. Settypalli, William G. Dundon, Siegfried Khaiseb, Mark Jago, Giovanni Cattoli, Charles E. Lamien
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Intestinibaculum porci gen. nov., sp. nov., a new member of the family Erysipelotrichaceae isolated from the small intestine of a swine
Ji-Sun Kim , Hanna Choe , Yu-Ri Lee , Kyung Mo Kim , Doo-Sang Park
J. Microbiol. 2019;57(5):381-387.   Published online February 22, 2019
DOI: https://doi.org/10.1007/s12275-019-8631-8
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AbstractAbstract
A strictly anaerobic, Gram-stain-positive, catalase-negative, non-motile, rod-shaped bacterium, designated SG0102T, was isolated from the small intestine of a swine. Optimal growth occurred at 37°C and pH 7.0. Furthermore, growth was observed in the presence of up to 3% (w/v) NaCl but not at salinity levels higher than 4%. The comparative analysis of 16S rRNA gene sequences showed that strain SG0102T was most closely related to Kandleria vitulina DSM 20405T (93.3%), followed by Catenibacterium mitsuokai KCTC 5053T (91.1%), Sharpea azabuensis KCTC 15217T (91.0%), and Eggerthia catenaformis DSM 5348T (89.6%). The average nucleotide identity values between strain SG0102T and related species, K. vitulina DSM 20405T, C. mitsuokai KCTC 5053T, S. azabuensis KCTC 15217T, and E. catenaformis DSM 5348T, were 71.0, 69.3, 70.0, and 69.2%, respectively. The phylogenetic analysis based on 16S rRNA gene sequence revealed that strain SG0102T belonged to the family Erysipelotrichaceae in the class Erysipelotrichia. The DNA G+C content of the strain SG0102T was 39.5 mol%. The major cellular fatty acids (> 10%) of strain SG0102T were C16:0, C16:0 dimethyl acetal, and C18:2 ω9/12c. The cell wall peptidoglycan of strain SG0102T contained the meso-diaminopimelic acid. The strain SG0102T produced lactic acid as a major end product of fermentation. These distinct phenotypic and phylogenetic properties suggest that strain SG0102T represents a novel species in a novel genus of the family Erysipelotrichaceae, for which the name Intestinibaculum porci gen. nov. sp. nov. is proposed. The type strain is SG0102T (= KCTC 15725T = NBRC 113396T).

Citations

Citations to this article as recorded by  
  • An Update on Novel Taxa and Revised Taxonomic Status of Bacteria Isolated from Domestic Animals Described in 2018 to 2021
    Erik Munson, Sara D. Lawhon, Claire R. Burbick, Amanda Zapp, Maia Villaflor, Elizabeth Thelen, Romney M. Humphries
    Journal of Clinical Microbiology.2023;[Epub]     CrossRef
  • Rumen microbial composition associated with the non‐glucogenic to glucogenic short‐chain fatty acids ratio in Holstein cows
    Shuhei Takizawa, Takumi Shinkai, Yosuke Kobayashi, Masahiro Masuda, Kenji Hashiba, Kota Uchisawa, Fuminori Terada
    Animal Science Journal.2023;[Epub]     CrossRef
  • The gut microbiome and resistome of conventionally vs. pasture-raised pigs
    Devin B. Holman, Katherine E. Gzyl, Arun Kommadath
    Microbial Genomics .2023;[Epub]     CrossRef
  • Copranaerobaculum intestinale gen. nov., sp. nov., a novel anaerobic bacterium isolated from human faeces
    Jun-Hui Feng, Yu-Xiao Chang, Liang-Hui Li, Meng-Meng Li, Zong-Yu Huang, Ni Han, Wen-Jun Li, Rui-Fu Yang, Ping-Hua Qu, Yu-Jing Bi
    International Journal of Systematic and Evolutionary Microbiology .2022;[Epub]     CrossRef
  • Differences in the Composition of the Rumen Microbiota of Finishing Beef Cattle Divergently Ranked for Residual Methane Emissions
    Paul E. Smith, Alan K. Kelly, David A. Kenny, Sinéad M. Waters
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • List of new names and new combinations previously effectively, but not validly, published
    Aharon Oren, George Garrity
    International Journal of Systematic and Evolutionary Microbiology .2020; 70(3): 1443.     CrossRef
Comparison of antibiotic resistance and copper tolerance of Enterococcus spp. and Lactobacillus spp. isolated from piglets before and after weaning
Xueting Zou , Mengwei Weng , Xu Ji , Rong Guo , Weijiang Zheng , Wen Yao
J. Microbiol. 2017;55(9):703-710.   Published online September 2, 2017
DOI: https://doi.org/10.1007/s12275-017-6241-x
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AbstractAbstract
In China, antimicrobials and copper are used extensively as growth-promoting agents for piglets. This study aimed to characterize the role of in-feed copper in the emergence of copper-tolerant and antibiotic-resistant Enterococcus and Lactobacillus isolates in Chinese pig farms. Feces of the same eight piglets from four litters at 7 and 55 days old and their mothers were traced in order to isolate Enterococcus spp. and Lactobacillus spp.. The minimum inhibitory concentrations of 10 antimicrobials and copper sulfate were determined using an agar dilution method. The feed levels of Cu2+ for lactating sows, suckling piglets, and weaned piglets were 6, 177, and 18 mg/kg, respectively. All the 136 Enterococcus isolates were sensitive to vancomycin; and the resistance rates to penicillin, enrofloxacin, and high level streptomycin resistance increased significantly after weaning. For the 155 Lactobacillus isolates, the resistance rates to ampicillin, chloramphenicol, tetracycline, and enrofloxacin were significantly higher in weaned piglets. The ratios of copper tolerant Enterococcus and Lactobacillus isolates both increased significantly after weaning (P < 0.05). A phenotypic correlation was observed after classifying the isolates into two groups (CuSO4 MIC50 < 16 or 􎃶􀁇16 for enterococci; CuSO4 MIC50 < 12 or 􎃶􀁇12 for lactobacilli) and comparing the antimicrobial-resistant percentage of two groups. On species level, a significant increase of E. faecalis to enrofloxacin was observed in line with the increase of copper MIC (P < 0.05). The findings revealed the changes of the antibiotic resistance and copper tolerance level of enterococci and lactobacilli between suckling and weaned piglets and demonstrated that there might be a strong association between in-feed copper and increased antibiotic resistance in enterococci and lactobacilli in Chinese intensive swine farms.

Citations

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  • Comparative Genome Analysis and Characterization of the Probiotic Properties of Lactic Acid Bacteria Isolated from the Gastrointestinal Tract of Wild Boars in the Czech Republic
    Katerina Kavanova, Iveta Kostovova, Monika Moravkova, Tereza Kubasova, Vladimir Babak, Magdalena Crhanova
    Probiotics and Antimicrobial Proteins.2024;[Epub]     CrossRef
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    Andreia Rebelo, Bárbara Duarte, Ana R. Freitas, Agostinho Almeida, Rui Azevedo, Edgar Pinto, Luísa Peixe, Patrícia Antunes, Carla Novais
    Science of The Total Environment.2023; 900: 165769.     CrossRef
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    Feng Zhang, Erhui Jin, Xiaodan Liu, Xu Ji, Hong Hu
    Animals.2022; 12(18): 2418.     CrossRef
  • Antibiotic Susceptibility, Resistance Gene Determinants and Corresponding Genomic Regions in Lactobacillus amylovorus Isolates Derived from Wild Boars and Domestic Pigs
    Monika Moravkova, Iveta Kostovova, Katerina Kavanova, Radko Pechar, Stanislav Stanek, Ales Brychta, Michal Zeman, Tereza Kubasova
    Microorganisms.2022; 11(1): 103.     CrossRef
  • Lactobacillus fermentum and Lactobacillus plantarum bioremediation ability assessment for copper and zinc
    Saeed Hasr Moradi Kargar, Najmeh Hadizadeh Shirazi
    Archives of Microbiology.2020; 202(7): 1957.     CrossRef
  • Selection and dissemination of antimicrobial resistance in Agri-food production
    Guyue Cheng, Jianan Ning, Saeed Ahmed, Junhong Huang, Rizwan Ullah, Boyu An, Haihong Hao, Menghong Dai, Lingli Huang, Xu Wang, Zonghui Yuan
    Antimicrobial Resistance & Infection Control.2019;[Epub]     CrossRef
Research Support, Non-U.S. Gov't
NOTE] Lysinibacillus jejuensis sp. nov., Isolated from Swinery Waste
Ji-Young Kim , So-Hyun Park , Duck-Chul Oh , Young-Ju Kim
J. Microbiol. 2013;51(6):872-876.   Published online December 19, 2013
DOI: https://doi.org/10.1007/s12275-013-2500-7
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AbstractAbstract
A Gram-positive, endospore-forming, rod-shaped bacterium, designated strain N2-5T, was isolated from swinery waste collected in Jeju, Republic of Korea. A phylogenetic analysis based on 16S rRNA gene sequences demonstrated that strain N2-5T formed a phyletic group within the phylum Firmicutes with less than 97.0% similarities to members of the genus Lysinibacillus, its nearest phylogenetic neighbors. The highest levels of sequence similarity to the isolate were observed against Lysinibacillus xylanilyticus XDB9T (96.8%), Lysinibacillus macroides LMG 18474T (95.6%), and Lysinibacillus parviboronicapiens BAM-582 T (95.6%). The organism grew optimally at 30°C and pH 7 and in the presence of 1–3% (w/v) NaCl. Strain N2-5T was chemotaxonomically characterized by possessing menaquinone-7 (MK-7) as the major menaquinone, and iso-C15:0 (54.9%), iso-C17:1ω10c (12.0%), and C16:1ω7c alcohol (11.8%) as the predominant fatty acids. The genomic DNA G+C content of the novel strain was 43.3 mol% and the cell-wall peptidoglycan was type A4α. The major polar lipids were diphosphatidylglycerol, phosphatidylglycerol, and phosphatidylethanolamine. Based on its phenotypic properties and phylogenetic data, strain N2-5T (=DSM 28310T =KCTC13837 T) represents a novel species in the genus Lysinibacillus, for which the name Lysinibacillus jejuensis sp. nov. is proposed.

Citations

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  • Distribution and Characterization of Quaternary Ammonium Biocides Resistant Bacteria in Different Soils, in South-Western China
    Ziyi Guo, Cunli Qin, Lilan Zhang
    Microorganisms.2024; 12(8): 1742.     CrossRef
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    Amit Yadav, Ruchi Teware, Agrima Bhatt, Yash Bhavsar, Akanksha Maurya, Vipool Thorat, Venkata Ramana Vemuluri, Kiran Kirdat
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    Archives of Microbiology.2020; 202(6): 1529.     CrossRef
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