Rapid detection by multiplex PCR of Genomic Islands, prophages and Integrative Conjugative Elements in V. cholerae 7th pandemic variants

2012 ◽  
Vol 88 (1) ◽  
pp. 98-102 ◽  
Author(s):  
Matteo Spagnoletti ◽  
Daniela Ceccarelli ◽  
Mauro M. Colombo
2009 ◽  
Vol 41 (3) ◽  
pp. 181 ◽  
Author(s):  
Junyoung Kim ◽  
Semi Jeon ◽  
Hogeun Rhie ◽  
Bokkwon Lee ◽  
Misun Park ◽  
...  

2004 ◽  
Vol 42 (6) ◽  
pp. 2821-2824 ◽  
Author(s):  
S. Chattopadhyay ◽  
R. Patra ◽  
T. Ramamurthy ◽  
A. Chowdhury ◽  
A. Santra ◽  
...  

2012 ◽  
Vol 11 (19) ◽  
pp. 3544-3549
Author(s):  
Zengqi Yang ◽  
Li Qiu ◽  
Chao Sun ◽  
Hu Yang ◽  
Chunli Li ◽  
...  

2021 ◽  
Vol 30 (4) ◽  
pp. 20-26
Author(s):  
Le Thanh Huong ◽  
Ha Thi Phuong Mai ◽  
Hoang Thi Thu Ha ◽  
Nguyen Dong Tu ◽  
Bui Tien Sy ◽  
...  

Listeria monocytogenes is widely present in the natural environment. This bacteria can cause infections in both humans and animals. In humans, the most vulnerable groups to be infected with L. monocytogenes are the elderly, people with an impaired immune system and chronically illness, pregnant women, and newborn babies. The aim of this study was to develop a multiplex PCR assay for the rapid detection of L. monocytogenes in mock clinical samples. A pair of primers were designed for detection of L. monocytogenes based on prs, a Listeria genus specific gene, and hly, a hemolysin gene. The specificity of the primers were tested by using different L. monocytogenes strains and other common pathogenic bacteria. The results showed that L. monocytogenes strains were positive in the detection and other tested strains were negative in mock (spiked) clinical samples. The sensitivity of multiplex PCR assay was 102 CFU/ml per reaction. The specificity and sensitivity of multiplex PCR technology for detecting L. monocytogenes in mock (spiked) clinical samples were high, and the assay could be completed within 1.5 hours. Therefore, this established multiplex PCR provides a rapid and reliable method and will be useful for the detection of L. monocytogenes in mock clinical samples.


2020 ◽  
Vol 117 (38) ◽  
pp. 23762-23773
Author(s):  
Archana Pant ◽  
Satyabrata Bag ◽  
Bipasa Saha ◽  
Jyoti Verma ◽  
Pawan Kumar ◽  
...  

Bacterial species are hosts to horizontally acquired mobile genetic elements (MGEs), which encode virulence, toxin, antimicrobial resistance, and other metabolic functions. The bipartite genome ofVibrio choleraeharbors sporadic and conserved MGEs that contribute in the disease development and survival of the pathogens. For a comprehensive understanding of dynamics of MGEs in the bacterial genome, we engineered the genome ofV. choleraeand examined in vitro and in vivo stability of genomic islands (GIs), integrative conjugative elements (ICEs), and prophages. Recombinant vectors carrying the integration module of these GIs, ICE and CTXΦ, helped us to understand the efficiency of integrations of MGEs in theV. choleraechromosome. We have deleted more than 250 acquired genes from 6 different loci in theV. choleraechromosome and showed contribution of CTX prophage in the essentiality of SOS response master regulator LexA, which is otherwise not essential for viability in other bacteria, includingEscherichia coli. In addition, we observed that the core genome-encoded RecA helps CTXΦ to bypassV. choleraeimmunity and allow it to replicate in the host bacterium in the presence of similar prophage in the chromosome. Finally, our proteomics analysis reveals the importance of MGEs in modulating the levels of cellular proteome. This study engineered the genome ofV. choleraeto remove all of the GIs, ICEs, and prophages and revealed important interactions between core and acquired genomes.


2002 ◽  
Vol 40 (4) ◽  
pp. 1436-1440 ◽  
Author(s):  
S. D. Belanger ◽  
M. Boissinot ◽  
C. Menard ◽  
F. J. Picard ◽  
M. G. Bergeron

LWT ◽  
2019 ◽  
Vol 116 ◽  
pp. 108474 ◽  
Author(s):  
Moutong Chen ◽  
Jianheng Cheng ◽  
Rui Pang ◽  
Jumei Zhang ◽  
Yuetao Chen ◽  
...  

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