Journal Articles
- Dynamics of Microbial Community Structure, Function and Assembly Mechanism with Increasing Stand Age of Slash Pine (Pinus elliottii) Plantations in Houtian Sandy Area, South China
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Xiaoyang Zhang , Si-Yi Xiong , Xiukun Wu , Bei-Bei Zeng , Yang-Mei Mo , Zhi-Cheng Deng , Qi Wei , Yang Gao , Licao Cui , Jianping Liu , Haozhi Long
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J. Microbiol. 2023;61(11):953-966. Published online November 29, 2023
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DOI: https://doi.org/10.1007/s12275-023-00089-7
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75
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Abstract
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Establishing slash pine plantations is the primary method for restoring sandification land in the Houtian area of South China.
However, the microbial variation pattern with increasing stand age remains unclear. In this study, we investigated microbial
community structure and function in bare sandy land and four stand age gradients, exploring ecological processes that
determine their assembly. We did not observe a significant increase in the absolute abundance of bacteria or fungi with stand
age. Bacterial communities were dominated by Chloroflexi, Actinobacteria, Proteobacteria, and Acidobacteria; the relative
abundance of Chloroflexi significantly declined while Proteobacteria and Acidobacteria significantly increased with stand
age. Fungal communities showed succession at the genus level, with Pisolithus most abundant in soils of younger stands
(1- and 6-year-old). Turnover of fungal communities was primarily driven by stochastic processes; both deterministic and
stochastic processes influenced the assembly of bacterial communities, with the relative importance of stochastic processes
gradually increasing with stand age. Bacterial and fungal communities showed the strongest correlation with the diameter
at breast height, followed by soil available phosphorus and water content. Notably, there was a significant increase in the
relative abundance of functional groups involved in nitrogen fixation and uptake as stand age increased. Overall, this study
highlights the important effects of slash pine stand age on microbial communities in sandy lands and suggests attention to
the nitrogen and phosphorus requirements of slash pine plantations in the later stages of sandy management.
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Citations
Citations to this article as recorded by

- Assembly processes and networks of soil microbial communities along karst forest succession
Wanxia Peng, Min Song, Hu Du, Shanghua Jiang, Fuping Zeng, Huijun Chen, Tongqing Song
CATENA.2025; 248: 108574. CrossRef - Temporal dynamics of soil microbial symbioses in the root zone of wolfberry: deciphering the effects of biotic and abiotic factors on bacterial and fungal ecological networks
Mengyuan He, Qianqian Wang, Yiming Wang, Junhua Zhang
Frontiers in Plant Science.2025;[Epub] CrossRef - Assessing the health of climate-sensitive trees in a subalpine ecosystem through microbial community dynamics
Bo Ram Kang, Soo Bin Kim, Jin-Kyung Hong, Seok Hyun Ahn, Jinwon Kim, Nayeon Lee, Tae Kwon Lee
Science of The Total Environment.2024; 957: 177724. CrossRef - The complex relationships between diatoms, bacterial communities, and dissolved organic matter: Effects of silicon concentration
Xiding Wang, Yang Liu, Yi Zhang, Peng Wu, Xudong Liu, Fangru Nan, Qi Liu, Junping Lv, Jia Feng, Shulian Xie
Algal Research.2024; 79: 103460. CrossRef - Assembly and co-occurrence pattern of microbial communities in bulk and rhizosphere soils of Pinus elliottii plantations on sandy lands in China
Haozhi Long, Si-Yi Xiong, Yang-Mei Mo, Bei-Bei Zeng, Bin-Xuan Shan, Ting Xiao, Yang Gao, Chaoyu Cui
Plant and Soil.2024;[Epub] CrossRef
- Analysis of phylogenetic markers for classification of a hydrogen peroxide producing Streptococcus oralis isolated from saliva by a newly devised differential medium
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Ha Pham , Thi Dieu Thuy Tran , Youri Yang , Jae-Hyung Ahn , Hor-Gil Hur , Yong-Hak Kim
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J. Microbiol. 2022;60(8):795-805. Published online July 14, 2022
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DOI: https://doi.org/10.1007/s12275-022-2261-2
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47
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Abstract
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Hydrogen peroxide (H2O2) is produced by alpha-hemolytic
streptococci in aerobic conditions. However, the suitable method
for detection of H2O2-producing streptococci in oral
microbiota has not been setup. Here we show that o-dianisidine
dye and horseradish peroxidase were useful in tryptic
soy agar medium to detect and isolate H2O2-producing
bacteria with the detection limit of one target colony in > 106
colony-forming units. As a proof, we isolated the strain HP01
(KCTC 21190) from a saliva sample using the medium and
analyzed its characteristics. Further tests showed that the strain
HP01 belongs to Streptococcus oralis in the Mitis group and
characteristically forms short-chain streptococcal cells with
a high capacity of acid tolerance and biofilm formation. The
genome analysis revealed divergence of the strain HP01 from
the type strains of S. oralis. They showed distinctive phylogenetic
distances in their ROS-scavenging proteins, including
superoxide dismutase SodA, thioredoxin TrxA, thioredoxin
reductase TrxB, thioredoxin-like protein YtpP, and glutaredoxin-
like protein NrdH, as well as a large number of antimicrobial
resistance genes and horizontally transferred genes.
The concatenated ROS-scavenging protein sequence can be
used to identify and evaluate Streptococcus species and subspecies
based on phylogenetic analysis.
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Citations
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- Alleviation of H2O2 toxicity by extracellular catalases in the phycosphere of Microcystis aeruginosa
Yerim Park, Wonjae Kim, Yeji Cha, Minkyung Kim, Woojun Park
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Review
- Minireview] Loop-mediated isothermal amplification (LAMP): principle, features, and future prospects
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Tsugunori Notomi , Yasuyoshi Mori , Norihiro Tomita , Hidetoshi Kanda
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J. Microbiol. 2015;53(1):1-5. Published online January 4, 2015
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DOI: https://doi.org/10.1007/s12275-015-4656-9
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78
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Abstract
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Loop-mediated isothermal amplification (LAMP), a newly developed gene amplification method, combines rapidity, simplicity, and high specificity. Several tests have been developed based on this method, and simplicity is maintained throughout all steps, from extraction of nucleic acids to detection of amplification. In the LAMP reaction, samples are amplified at a fixed temperature through a repetition of two types of elongation reactions occurring at the loop regions: self-elongation of templates from the stem loop structure formed at the 3'-terminal and the binding and elongation of new primers to the loop region. The LAMP reaction has a wide range of possible applications, including point-of-care testing, genetic testing in resource-poor settings (such as in developing countries), and rapid testing of food products and environmental samples.
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Annals of Laboratory Medicine.2018; 38(2): 119. CrossRef - A field survey using LAMP assay for detection of Schistosoma mansoni in a low-transmission area of schistosomiasis in Umbuzeiro, Brazil: Assessment in human and snail samples
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PLOS Neglected Tropical Diseases.2018; 12(3): e0006314. CrossRef - A rapid and eco-friendly isothermal amplification microdevice for multiplex detection of foodborne pathogens
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Analytical Chemistry.2018; 90(12): 7221. CrossRef - Application of the LAMP assay for the detection of the Argentine ant, Linepithema humile (Hymenoptera: Formicidae), from captures of pan traps
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Applied Entomology and Zoology.2018; 53(2): 275. CrossRef - Lineage specific detection of the scaly form of the pen shell Atrina spp. by a loop-mediated isothermal amplification method
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Fisheries Science.2018; 84(5): 837. CrossRef - Diagnosis of amphimeriasis by LAMPhimerus assay in human stool samples long-term storage onto filter paper
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Molecular Ecology Resources.2018; 18(2): 251. CrossRef - Exponential Isothermal Amplification of Nucleic Acids and Assays for Proteins, Cells, Small Molecules, and Enzyme Activities: An EXPAR Example
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Angewandte Chemie International Edition.2018; 57(37): 11856. CrossRef - Loop-mediated isothermal amplification (LAMP) shield for Arduino DNA detection
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Sensors.2018; 18(10): 3423. CrossRef - Chromogenic detection of yam mosaic virus by closed-tube reverse transcription loop-mediated isothermal amplification (CT-RT-LAMP)
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PLOS Neglected Tropical Diseases.2018; 12(2): e0006264. CrossRef - Community-Acquired Pneumonia in Children: the Challenges of Microbiological Diagnosis
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Acta Tropica.2018; 178: 86. CrossRef - Detection of HCV genotypes 1b and 2a by a reverse transcription loop‐mediated isothermal amplification assay
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Scientific Reports.2017;[Epub] CrossRef - Microbial genomics and antimicrobial susceptibility testing
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BioChip Journal.2017; 11(1): 8. CrossRef - Development of a Quantitative Loop-Mediated Isothermal Amplification Assay for the Rapid Detection of Novel Goose Parvovirus
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William Cevallos, Pedro Fernández-Soto, Manuel Calvopiña, Cristina Fontecha-Cuenca, Hiromu Sugiyama, Megumi Sato, Julio López Abán, Belén Vicente, Antonio Muro, David Blair
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Nanoscale.2017; 9(5): 1852. CrossRef - Loop‐mediated isothermal amplification (LAMP) as an alternative to PCR: A rapid on‐site detection of gene doping
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Journal of Food Quality.2017; 2017: 1. CrossRef - Development of a recombinase polymerase amplification lateral flow dipstick (RPA-LFD) for the field diagnosis of caprine arthritis-encephalitis virus (CAEV) infection
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Nematology.2017; 19(5): 559. CrossRef - A smart sealed nucleic acid biosensor based on endogenous reference gene detection to screen and identify mammals on site
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PeerJ.2017; 5: e3799. CrossRef - Sequence-specific validation of LAMP amplicons in real-time optomagnetic detection of Dengue serotype 2 synthetic DNA
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Molecular Medicine Reports.2017; 15(5): 3203. CrossRef - Colorimetric tests for diagnosis of filarial infection and vector surveillance using non-instrumented nucleic acid loop-mediated isothermal amplification (NINA-LAMP)
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Korean Journal of Chemical Engineering.2017; 34(10): 2678. CrossRef - Rapid on-site evaluation of the development of resistance to quinone outside inhibitors in Botrytis cinerea
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Molecular Ecology Resources.2017; 17(2): 138. CrossRef - Rapid and Sensitive Detection of sFAT-1 Transgenic Pigs by Visual Loop-Mediated Isothermal Amplification
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Applied Biochemistry and Biotechnology.2016; 179(6): 938. CrossRef - Peste des petits ruminants diagnosis and diagnostic tools at a glance: perspectives on global control and eradication
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Archives of Virology.2016; 161(11): 2953. CrossRef - Molecular Identification of an Invasive Wood-Boring InsectLyctus brunneus(Coleoptera: Bostrichidae: Lyctinae) Using Frass by Loop-Mediated Isothermal Amplification and Nested PCR Assays
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Bioorganic & Medicinal Chemistry Letters.2016; 26(3): 841. CrossRef - A field-deployable mobile molecular diagnostic system for malaria at the point of need
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Frontiers in Microbiology.2016;[Epub] CrossRef - Molecular Identification of the Western Drywood Termite (Isoptera: Kalotermitidae) by Loop-Mediated Isothermal Amplification of DNA from Fecal Pellets
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Journal of Economic Entomology.2016; 109(5): 2234. CrossRef - An Innovative Method for Rapid Identification and Detection of Vibrio alginolyticus in Different Infection Models
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Frontiers in Microbiology.2016;[Epub] CrossRef - Rapid authentication of the precious herb saffron by loop-mediated isothermal amplification (LAMP) based on internal transcribed spacer 2 (ITS2) sequence
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Frontiers in Plant Science.2016;[Epub] CrossRef - A novel microfluidic device that integrates nucleic acid extraction, amplification, and detection to identify an EGFR mutation in lung cancer tissues
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Nan Cheng, Yuancong Xu, Xinghua Yan, Ying Shang, Pengyu Zhu, Wenying Tian, Zhihong Liang, Wentao Xu
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Hehe Wang, William W. Turechek, Tzong-Yueh Chen
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Anneke van der Zee, Joop F. P. Schellekens, Frits R. Mooi
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Yongxi Zhao, Feng Chen, Qian Li, Lihua Wang, Chunhai Fan
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Lei Zhang, Rachel N. Deraney, Anubhav Tripathi
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Research Support, Non-U.S. Gov't
- Improved Prediction of Coreceptor Usage and Phenotype of HIV-1 Based on Combined Features of V3 Loop Sequence Using Random Forest
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Shungao Xu , Xinxiang Huang , Huaxi Xu , Chiyu Zhang
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J. Microbiol. 2007;45(5):441-446.
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DOI: https://doi.org/2592 [pii]
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Abstract
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HIV-1 coreceptor usage and phenotype mainly determined by V3 loop are associated with the disease progression of AIDS. Predicting HIV-1 coreceptor usage and phenotype facilitates the monitoring of R5-to-X4 switch and treatment decision-making. In this study, we employed random forest to predict HIV-1 biological phenotype, based on 37 random features of V3 loop. In comparison with PSSM method, our RF predictor obtained higher prediction accuracy (95.1% for coreceptor usage and 92.1% for phenotype), especially for non-B non-C HIV-1 subtypes (96.6% for coreceptor usage and 95.3% for phenotype). The net charge, polarity of V3 loop and five V3 sites are seven most important features for predicting HIV-1 coreceptor usage or phenotype. Among these features, V3 polarity and four V3 sites (22, 12, 18 and 13) are first reported to have high contribution to HIV-1 biological phenotype prediction.
- Mutational analysis of P2 structure in T4 phage td intron
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Shin, sook , Park, In kook
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J. Microbiol. 1995;33(1):91-94.
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Abstract
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The functional role of P2 stem-loop structure of T4 td intron in splicing in vivo and in vitro was investigated. Site-directed mutagenesis was employed to create the subtitution, deletion and reversion mutants of P2 stem=loop structure. Two substitution mutation(U16→G, A31→C) and on deletion mutation (G21□C26) resulted in a complete loss of enzyme activity whereas the compensatory double mutation restored about 82% of activity of the wild type. The transcription rate of two substitution mutations and P2 loop deletion is lower than that of the wild type. The disruption of P2 stem-loop structure by introducing substitution and deletion mutation resulted in a complete abolishment of Rna splicing in bitro. However, a compensatory double mutation showed splicing activity very similar to the wild type.
- Mutational Analysis of an Essential RNA Stem-loop Structure in a Minimal RNA Substrate Specifically Cleaved by Leishmania RNA Virus 1-4 (LRV1-4) Capsid Endoribonuclease
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Youngtae Ro , Jean L. Patterson
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J. Microbiol. 2003;41(3):239-247.
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Abstract
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The LRV1-4 capsid protein possesses an endoribonuclease activity that is responsible for the single sitespecific cleavage in the 5’ untranslated region (UTR) of its own viral RNA genome and the formation of a conserved stem-loop structure (stem-loop IV) in the UTR is essential for the accurate RNA cleavage by the capsid protein. To delineate the nucleotide sequences, which are essential for the correct formation of the stem-loop structure for the accurate RNA cleavage by the viral capsid protein, a wildtype minimal RNA transcript (RNA 5’ 249-342) and several synthetic RNA transcripts encoding pointmutations in the stem-loop region were generated in an in vitro transcription system, and used as substrates for the RNA cleavage assay and RNase mapping studies. When the RNA 5’ 249-342 transcript was subjected to RNase T1 and A mapping studies, the results showed that the predicted RNA secondary structure in the stem-loop region using FOLD analysis only existed in the presence of Mg2+ ions, suggesting that the metal ion stabilizes the stem-loop structure of the substrate RNA in solution. When point-mutated RNA substrates were used in the RNA cleavage assay and RNase T1 mapping study, the specific nucleotide sequences in the stem-loop region were not required for the accurate RNA cleavage by the viral capsid protein, but the formation of a stem-loop like structure in a region (nucleotides from 267 to 287) stabilized by Mg_2^+ ions was critical for the accurate RNA cleavage. The RNase T1 mapping and EMSA studies revealed that the Ca2+ and Mn2+ ions, among the reagents tested, could change the mobility of the substrate RNA 5’ 249-342 on a gel similarly to that of Mg_2^+ ions, but only Ca_2^+ ions identically showed the stabilizing effect of Mg_2^+ ions on the stem-loop structure, suggesting that binding of the metal ions (Mg_2^+ or Ca_2^+) onto the RNA substrate in solution causes change and stabilization of the RNA stem-loop structure, and only the substrate RNA with a rigid stem-loop structure in the essential region can be accurately cleaved by the LRV1-4 viral capsid protein.