Javascript must be enabled to continue!
Enterobacterial repetitive intergenic consensus (ERIC)-PCR analysis as a trace for Burkholderia pseudomallei in Myanmar
View through CrossRef
Melioidosis is a potentially fatal disease caused by Burkholderia pseudomallei, which is endemic in Southeast Asia, including Myanmar. The typeability of enterobacterial repetitive intergenic consensus (ERIC)-PCR assessed for 21 B. pseudomallei, they used the results of sequence types (STs) of the multilocus sequence typing (MLST) method. Among 5 soil and 16 clinical B. pseudomallei isolates, the most significant bands were similar in position but different in minor band formation. ST 90 of two soil strains (Tontae_NMBP001 and Tontae_NMBP002) displayed the same ERIC banding pattern, while ST 56 of two clinical isolates (MMBP005 and MMBP010) from different regions exhibited a single type. The same ST found both clusters in the MLST method. The shared group STs showed four or three satellite variants in the MLST scheme. One novel studied ST (ST 1729) and regarded it as an out-group in the ERIC pattern. ERIC PCR demonstrated high discriminatory power, while MLST provided more discrimination for genetic diversity. MLST requires extensive sequencing and bioinformatics analysis, making it challenging to implement in resource-limited settings. More isolates are needed to validate these findings. Despite its limitations, ERIC PCR represents a valuable and cost-effective alternative to MLST for molecular typing of B. pseudomallei in resource-limited settings.
Cold Spring Harbor Laboratory
Title: Enterobacterial repetitive intergenic consensus (ERIC)-PCR analysis as a trace for Burkholderia pseudomallei in Myanmar
Description:
Melioidosis is a potentially fatal disease caused by Burkholderia pseudomallei, which is endemic in Southeast Asia, including Myanmar.
The typeability of enterobacterial repetitive intergenic consensus (ERIC)-PCR assessed for 21 B.
pseudomallei, they used the results of sequence types (STs) of the multilocus sequence typing (MLST) method.
Among 5 soil and 16 clinical B.
pseudomallei isolates, the most significant bands were similar in position but different in minor band formation.
ST 90 of two soil strains (Tontae_NMBP001 and Tontae_NMBP002) displayed the same ERIC banding pattern, while ST 56 of two clinical isolates (MMBP005 and MMBP010) from different regions exhibited a single type.
The same ST found both clusters in the MLST method.
The shared group STs showed four or three satellite variants in the MLST scheme.
One novel studied ST (ST 1729) and regarded it as an out-group in the ERIC pattern.
ERIC PCR demonstrated high discriminatory power, while MLST provided more discrimination for genetic diversity.
MLST requires extensive sequencing and bioinformatics analysis, making it challenging to implement in resource-limited settings.
More isolates are needed to validate these findings.
Despite its limitations, ERIC PCR represents a valuable and cost-effective alternative to MLST for molecular typing of B.
pseudomallei in resource-limited settings.
Related Results
Isolation and characterization of bacteriophages against Burkholderia species
Isolation and characterization of bacteriophages against Burkholderia species
Abstract
Burkholderia cepacia complex (Bcc) is a potent nosocomial pathogen mainly encountered in immunocompromised, cystic fibrosis and chronic granulomatous patients. The...
Melioidosis in Africa: Time to Uncover the True Disease Load
Melioidosis in Africa: Time to Uncover the True Disease Load
Melioidosis is an often fatal infectious disease with a protean clinical spectrum, caused by the environmental bacterial pathogen Burkholderia pseudomallei. Although the disease ha...
Burkholderia humisilvae sp. nov., Burkholderia solisilvae sp. nov. and Burkholderia rhizosphaerae sp. nov., isolated from forest soil and rhizosphere soil
Burkholderia humisilvae sp. nov., Burkholderia solisilvae sp. nov. and Burkholderia rhizosphaerae sp. nov., isolated from forest soil and rhizosphere soil
Strains Y-12T and Y-47T were isolated from mountain forest soil and strain WR43T was isolated from rhizosphere soil, at Daejeon, Korea. The three strains grew at 10–55 °C (optimal ...
1711. In Vitro Activity of Cefiderocol Against US Achromobacter spp. and Burkholderia spp. Clinical Isolates from the SENTRY Surveillance Program 2020-2021
1711. In Vitro Activity of Cefiderocol Against US Achromobacter spp. and Burkholderia spp. Clinical Isolates from the SENTRY Surveillance Program 2020-2021
Abstract
Background
Infections caused by Achromobacter spp. and Burkholderia spp. have limited clinical treatment options due to...
Genetic diversity, determinants, and dissemination of Burkholderia pseudomallei lineages implicated in melioidosis in Northeast Thailand
Genetic diversity, determinants, and dissemination of Burkholderia pseudomallei lineages implicated in melioidosis in Northeast Thailand
AbstractMelioidosis is an often-fatal neglected tropical disease caused by an environmental bacterium Burkholderia pseudomallei. However, our understanding of the disease-causing b...
Earning vs Learning: Supporting Myanmar Migrant Education on the Thailand Myanmar Border
Earning vs Learning: Supporting Myanmar Migrant Education on the Thailand Myanmar Border
<p><b>This thesis examines a particular case study of a Migrant Learning Centre on the Thailand Myanmar Border. Previous research has identified a variety of access to ...
Disaster diplomacy : a case study of the tripartite core group's post-nargis humanitarian assistance in Myanmar
Disaster diplomacy : a case study of the tripartite core group's post-nargis humanitarian assistance in Myanmar
On 2 May 2008 the devastating Cyclone Nargis hit Myanmar, causing over 140,000 deaths and affecting about 2.4 million people in the country. Despite the desperate situation, the Go...
Abstract 2113: A wild-type-blocking reference sequence enhances COLD-PCR and enables fast amplification and high enrichment of all types of low-prevalence unknown mutations
Abstract 2113: A wild-type-blocking reference sequence enhances COLD-PCR and enables fast amplification and high enrichment of all types of low-prevalence unknown mutations
Abstract
Background: Molecular profiling of somatic mutations in cancer often requires the identification of low-prevalence DNA mutations in an excess of wild-type (...

