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Critical Reviews™ in Immunology

Publicou 6 edições por ano

ISSN Imprimir: 1040-8401

ISSN On-line: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

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Sensitive Molecular Diagnostic Assays to Mitigate the Risks of Asymptomatic Bacterial Diseases of Plants

Volume 30, Edição 3, 2010, pp. 271-275
DOI: 10.1615/CritRevImmunol.v30.i3.40
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RESUMO

Our highly concentrated monoculture makes crops vulnerable to pests and diseases. An increase in emerging non-indigenous bacterial diseases poses a real threat to US agriculture. The United States has 100,000 miles of shoreline and 6,000 miles of border, making possible easy introduction of crop pests and diseases. Most threatening to crops are the cross-domain enteric bacteria. In contrast to animals, crops have hundreds of major diseases and development of molecular-based detection protocols for each pathogen is impossible with current technology. Rathayibacter toxicus, a neurotoxin-producing bacterium transmitted by a seed gall nematode, is an example of a high-risk Select Agent. The bacterium infects seeds of grasses without showing any symptoms, often resulting in the death of grazing cattle. A prerequisite for the control of any disease is sensitive detection and proper identification of the causal organism. Detecting bacteria in samples of plants showing symptoms is relatively simple, whereas detection in asymptomatic tissues is difficult due to the extremely low numbers of the target pathogen present. Rapid serological assays work well with symptomatic tissues but not from asymptomatic tissue when bacteria levels are below sensitivity limits. Classical agar-plating assays are 1,000 fold more sensitive then serology or PCR. However, agar plating assays take from 3 to 5 days and require pathogenicity tests to confirm the identity. PCR-based assays allow for rapid, accurate identification but are insensitive due to use of 1 μL sample in comparison to 100 μL used for agar plating. To overcome this disadvantage, an enrichment technique termed BIO-PCR can be used in combination with agar plating for detection with asymptomatic tissues. The key to developing a successful BIO-PCR protocol is to determine the time required for development of pin point-size colonies to appear. For most plant pathogens 15 to 24 hours is sufficient time, whereas for the cross-domain bacteria only 1 to 2 hours is needed. For greater sensitivity, BIO-PCR can be combined with 96-well microliter plates with membranes to detect a single viable cell per 10 mL of an aqueous sample.

CITADO POR
  1. Paquet Valérie E., Charette Steve J., Kümmerli Rolf, Amoeba-resisting bacteria found in multilamellar bodies secreted byDictyostelium discoideum:social amoebae can also package bacteria, FEMS Microbiology Ecology, 92, 3, 2016. Crossref

  2. Charlermroj Ratthaphol, Makornwattana Manlika, Himananto Orawan, Seepiban Channarong, Phuengwas Sudtida, Warin Nuchnard, Gajanandana Oraprapai, Karoonuthaisiri Nitsara, An accurate, specific, sensitive, high-throughput method based on a microsphere immunoassay for multiplex detection of three viruses and bacterial fruit blotch bacterium in cucurbits, Journal of Virological Methods, 247, 2017. Crossref

  3. Ivanov Aleksandr V., Safenkova Irina V., Drenova Natalia V., Zherdev Anatoly V., Dzantiev Boris B., Development of lateral flow assay combined with recombinase polymerase amplification for highly sensitive detection of Dickeya solani, Molecular and Cellular Probes, 53, 2020. Crossref

  4. Lacroix Christelle, Renner Kurra, Cole Ellen, Seabloom Eric W., Borer Elizabeth T., Malmstrom Carolyn M., Schaffner D. W., Methodological Guidelines for Accurate Detection of Viruses in Wild Plant Species, Applied and Environmental Microbiology, 82, 6, 2016. Crossref

  5. Hu Wei-Wei, He Jian-Wei, Guo Shu-Liang, Li Jin, Development and evaluation of a rapid and sensitive multienzyme isothermal rapid amplification with a lateral flow dipstick assay for detection of Acinetobacter baumannii in spiked blood specimens, Frontiers in Cellular and Infection Microbiology, 12, 2022. Crossref

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