1970
DOI: 10.13057/biodiv/d120101
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Identification and characterization of Salmonella typhi isolates from Southwest Sumba District, East Nusa Tenggara based on 16S rRNA gene sequences

Abstract: The incidence rate of typhoid fever in the Southwest Sumba District, East Nusa Tenggara was approximately about 725/100,000. In spite of such rate, there was not much known-yet about the molecular epidemiology of the disease. Thus, having accurate data and a strong discriminatory ability was crucial to scrutinize the molecular epidemiology of S. typhi with a molecular phylogenetic approach based on 16S rRNA gene sequences. Sixteen isolates representative of S. typhi from different geographical regions in South… Show more

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Cited by 5 publications
(4 citation statements)
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“…Preparation of pathogenic bacteria. Three pathogenic bacteria consisting of Salmonella typhi BPE 122.4 CCA, was obtained from previous research collections [11] [12], Salmonella typhi NCTC 786, which was obtained from PT Biofarma, and Staphylococcus aureus ATCC 25923 was cultured in BHI broth (Merck) at 37ºC for 16-18 hours [3]. Meanwhile, the cells are harvested through a centrifugation process at a speed of 13.500 rpm for 15 minutes.…”
Section: Determination Of Bacteriocin Activitymentioning
confidence: 99%
“…Preparation of pathogenic bacteria. Three pathogenic bacteria consisting of Salmonella typhi BPE 122.4 CCA, was obtained from previous research collections [11] [12], Salmonella typhi NCTC 786, which was obtained from PT Biofarma, and Staphylococcus aureus ATCC 25923 was cultured in BHI broth (Merck) at 37ºC for 16-18 hours [3]. Meanwhile, the cells are harvested through a centrifugation process at a speed of 13.500 rpm for 15 minutes.…”
Section: Determination Of Bacteriocin Activitymentioning
confidence: 99%
“…The pathogenic bacteria used were Gram-positive, specifically Staphylococcus aureus ATCC 25923. However, Salmonella typhi 122.4 CCA [15] and Salmonella typhi NCTC 786 obtained from PT. Biofarma were equally used.…”
Section: Pathogenic Bacteria Strain Preparationmentioning
confidence: 99%
“…These methods are the most popular and reliable in differentiating DEC strain from those of non-pathogenic bacteria. Moreover, the phylogeny and taxonomy of bacteria can also be studied using 16S rRNA gene sequence as genetic markers (Fujioka et al 2009;Amarantini et al 2011;Botkin et al 2012;Fialho et al 2013;Suardana 2014). The gene sequence of 16S rRNA is used because 16S rRNA gene is found in almost all bacteria, 16S rRNA gene does not change its function over time, and 16S rRNA gene (1500 bp) is large enough for information purposes.…”
Section: Introductionmentioning
confidence: 99%
“…Characteristics of molecular targets from these methods allow the study of bacterial phylogenetic, both for bacteria detection or identification in clinical laboratories (Rahmani et al 2006;Amarantini et al 2011;Rinanda 2011;Suardana 2014;Ghazali and Rashid 2019). This research aims to study nucleotide sequence of 16S rRNA gene of pathogenic E. coli isolated from cow meat in Yogyakarta using Polymerase Chain Reaction (PCR).…”
Section: Introductionmentioning
confidence: 99%