Single-tube multiplex real-time PCR assay for rapid and reliable detection of HLA-A*31:01 allele

2018 ◽  
Vol 19 (10) ◽  
pp. 837-846 ◽  
Author(s):  
Tingting Zhang ◽  
Ying Xiao ◽  
Yanxia Wang ◽  
Yanwei Li ◽  
Lirong Zhang ◽  
...  
Author(s):  
Kundan Tandel ◽  
Mahadevan Kumar ◽  
G.S. Bhalla ◽  
S.P.S. Shergill ◽  
Vijaya Swarnim ◽  
...  

Plant Disease ◽  
2019 ◽  
Vol 103 (12) ◽  
pp. 3031-3040 ◽  
Author(s):  
Shabnam Rahimi-Khameneh ◽  
Sanni Hsieh ◽  
Renlin Xu ◽  
Tyler J. Avis ◽  
Sean Li ◽  
...  

Bacterial diseases of onion are reported to cause significant economic losses. Pantoea allii Brady, one of the pathogens causing the center rot on onions, has not yet been reported in Canada. We report the pathogenicity of P. allii on commercially available Canadian green onions (scallions). All P. allii-inoculated plants, irrespective of the inoculum concentration, exhibited typical leaf chlorotic discoloration on green onion leaves, which can reduce their marketability. Reisolation of P. allii from infected scallion tissues and reidentification by sequencing and phylogenetic analyses of the leuS gene suggest that the pathogen can survive in infected tissues 21 days after inoculation. This is the first report of P. allii as a potential pathogen of green onions. This study also reports the development and validation of a TaqMan real-time PCR assay targeting the leuS gene for reliable detection of P. allii in pure cultures and in planta. A 642-bp leuS gene fragment was targeted because it showed high nucleotide diversity and positively correlated with genome-based average nucleotide identity with respect to percent similarity index and identity of Pantoea species. The assay specificity was validated using 61 bacterial and fungal strains. Under optimal conditions, the selected primers and FAM-labeled TaqMan probe were specific for the detection of nine reference P. allii strains by real-time PCR. The 52 strains of other Pantoea spp. (n = 25), non-Pantoea spp. (n = 20), and fungi/oomycetes (n = 7) tested negative (no detectable fluorescence). Onion tissues spiked with P. allii, naturally infested onion bulbs, greenhouse infected green onion leaf samples, as well as an interlaboratory blind test were used to validate the assay specificity. The sensitivities of a 1-pg DNA concentration and 30 CFU are comparable to previously reported real-time PCR assays of other bacterial pathogens. The TaqMan real-time PCR assay developed in this study will facilitate reliable detection of P. allii and could be a useful tool for screening onion imports or exports for the presence of this pathogen.


2017 ◽  
Vol 18 (9) ◽  
pp. 853-963 ◽  
Author(s):  
Huijuan Wang ◽  
Xing Kang ◽  
Shaohe Zhou ◽  
Rong Chen ◽  
Zhengbin Liu ◽  
...  

2019 ◽  
Vol 72 (7) ◽  
pp. 487-492 ◽  
Author(s):  
Samson S Y Wong ◽  
Rosana W S Poon ◽  
Kelvin K W To ◽  
Jasper F W Chan ◽  
Gang Lu ◽  
...  

AimsHelminth infections are becoming uncommon in high-income countries and laboratory staff may lose expertise in their morphological identification, especially in histological sections where speciation of helminths is challenging. Commercially available molecular diagnostic panels for faecal specimens only offer tests for protozoa but not helminths. We aim to improve the identification accuracy of helminths using a multiplex PCR assay.MethodsWe designed three pairs of PCR primers and probes targeting multicopy genes for a multiplex single-tube real-time PCR assay which covers 16 trematode (28S rRNA gene), 24 cestode (cox1 gene) and 33 nematode (cox1 gene) species. Helminths (n=27) from faecal samples (n=10), fresh parasites (n=11), formalin-fixed specimens (n=4), cerebrospinal fluid (n=1) and bile (n=1) were examined morphologically and tested by PCR. Fifty stool samples negative for parasites by microscopy were also tested.ResultsThe PCR assay correctly identified the genera of all tested helminths. Agarose gel electrophoresis and sequencing of the purified PCR amplicons confirmed that the PCR products were of correct sizes with 100% correlation with the respective species. Sequencing of the cox1 gene failed to identify Capillaria spp. in one sample owing to the lack of corresponding sequences in GenBank. PCR and sequencing of the nematode 18S rRNA gene using consensus primers showed 100% homology with Capillaria spp. sequence. No positive PCR products were found in the negative stool samples.ConclusionsThe highly specific test correctly identified all helminths in our cohort. It is a useful adjunct to helminth identification in difficult situations such as histological sections.


Cytotherapy ◽  
2014 ◽  
Vol 16 (4) ◽  
pp. S45
Author(s):  
K. Janetzko ◽  
G. Rink ◽  
A. Hecker ◽  
K. Bieback ◽  
H. Klueter ◽  
...  

2014 ◽  
Vol 5 (1) ◽  
pp. 48-52 ◽  
Author(s):  
Chelsea L. Wright ◽  
Wayne L. Hynes ◽  
Breanna T. White ◽  
Mindy N. Marshall ◽  
Holly D. Gaff ◽  
...  

Tuberculosis ◽  
2018 ◽  
Vol 112 ◽  
pp. 120-125 ◽  
Author(s):  
Kenneth Siu-Sing Leung ◽  
Gilman Kit-Hang Siu ◽  
Kingsley King-Gee Tam ◽  
Pak-Leung Ho ◽  
Samson Sai-Yin Wong ◽  
...  

2014 ◽  
Vol 41 (1) ◽  
pp. 9-9 ◽  
Author(s):  
Karin Janetzko ◽  
Gabi Rink ◽  
Andrea Hecker ◽  
Karen Bieback ◽  
Harald Klüter ◽  
...  

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