Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State

Background: The presence of pathogenic bacteria in circulated currency was recorded as a public health hazard. In this study, all examined Sudanese banknotes (100%) were found to be contaminated by gram-negative bacteria. Proteus mirabilis were recovered from 10 examined notes (22.2%, f = 10), E. co...

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Main Authors: Alaa Abdalla Mukhtar, Noha Ahmed Abd Alfadil, Malik Suliman Mohamed, Hisham N Altayb, Salaheldein G Elzaki, Mohamed Salih Hassan
Format: Article
Language:English
Published: Knowledge E 2018-09-01
Series:Sudan Journal of Medical Sciences
Subjects:
Online Access:https://doi.org/10.18502/sjms.v13i3.2955
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author Alaa Abdalla Mukhtar
Noha Ahmed Abd Alfadil
Malik Suliman Mohamed
Hisham N Altayb
Salaheldein G Elzaki
Mohamed Salih Hassan
author_facet Alaa Abdalla Mukhtar
Noha Ahmed Abd Alfadil
Malik Suliman Mohamed
Hisham N Altayb
Salaheldein G Elzaki
Mohamed Salih Hassan
author_sort Alaa Abdalla Mukhtar
collection DOAJ
description Background: The presence of pathogenic bacteria in circulated currency was recorded as a public health hazard. In this study, all examined Sudanese banknotes (100%) were found to be contaminated by gram-negative bacteria. Proteus mirabilis were recovered from 10 examined notes (22.2%, f = 10), E. coli (13.3%, f = 6) and Klebsiella spp. (8.9%, f = 4) were also identified. Only the most resistant P. mirabilis isolate was identified using culture-based and 16S rRNA gene sequencing techniques. Methods: Proteus isolates were identified phenotypically and tested for their susceptibility to 16 of commonly used antibiotics, then most resistant isolate was confirmed genotypically via 16S rRNA gene amplification and sequencing. Bioinformatics analysis using BLAST for sequence similarity search, Clustal W program for multiple sequence alignment, MEGA7 software for phylogenetic analysis. Tree was constructed to show the evolutionary relationships of the obtained sequence with similar sequences in the databases using. Results: The obtained sequence was found to be 100% identical to P. mirabilis 16S rRNA gene using BLAST. The phylogenetic tree was constructed to show the evolutionary relationships of the obtained sequence with similar sequences in the databases using MEGA7 software, and the closest strain was found to be P. mirabilis strain from India (EU411047). Conclusion: This study has shown that some currency notes circulated at Khartoum transportation are carriers of antimicrobial-resistant P. mirabilis that could be potential source for their transmission in public.
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spelling doaj.art-bbea316c5bc64e9aa23464c373e887432022-12-21T22:31:05ZengKnowledge ESudan Journal of Medical Sciences1858-50512018-09-011311210.18502/sjms.v13i3.2955sjms.v13i3.2955Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum StateAlaa Abdalla Mukhtar0Noha Ahmed Abd Alfadil1Malik Suliman Mohamed2Hisham N Altayb3Salaheldein G Elzaki4Mohamed Salih Hassan5 Applied Bioinformatics Center, Africa City of Technology, Khartoum, Sudan Applied Bioinformatics Center, Africa City of Technology, Khartoum, Sudan Applied Bioinformatics Center, Africa City of Technology, Khartoum, Sudan Applied Bioinformatics Center, Africa City of Technology, Khartoum, Sudan Applied Bioinformatics Center, Africa City of Technology, Khartoum, Sudan Applied Bioinformatics Center, Africa City of Technology, Khartoum, SudanBackground: The presence of pathogenic bacteria in circulated currency was recorded as a public health hazard. In this study, all examined Sudanese banknotes (100%) were found to be contaminated by gram-negative bacteria. Proteus mirabilis were recovered from 10 examined notes (22.2%, f = 10), E. coli (13.3%, f = 6) and Klebsiella spp. (8.9%, f = 4) were also identified. Only the most resistant P. mirabilis isolate was identified using culture-based and 16S rRNA gene sequencing techniques. Methods: Proteus isolates were identified phenotypically and tested for their susceptibility to 16 of commonly used antibiotics, then most resistant isolate was confirmed genotypically via 16S rRNA gene amplification and sequencing. Bioinformatics analysis using BLAST for sequence similarity search, Clustal W program for multiple sequence alignment, MEGA7 software for phylogenetic analysis. Tree was constructed to show the evolutionary relationships of the obtained sequence with similar sequences in the databases using. Results: The obtained sequence was found to be 100% identical to P. mirabilis 16S rRNA gene using BLAST. The phylogenetic tree was constructed to show the evolutionary relationships of the obtained sequence with similar sequences in the databases using MEGA7 software, and the closest strain was found to be P. mirabilis strain from India (EU411047). Conclusion: This study has shown that some currency notes circulated at Khartoum transportation are carriers of antimicrobial-resistant P. mirabilis that could be potential source for their transmission in public.https://doi.org/10.18502/sjms.v13i3.2955Proteus mirabilis, banknotes, 16S rRNA, Khartoum State
spellingShingle Alaa Abdalla Mukhtar
Noha Ahmed Abd Alfadil
Malik Suliman Mohamed
Hisham N Altayb
Salaheldein G Elzaki
Mohamed Salih Hassan
Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
Sudan Journal of Medical Sciences
Proteus mirabilis, banknotes, 16S rRNA, Khartoum State
title Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
title_full Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
title_fullStr Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
title_full_unstemmed Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
title_short Identification of Proteus mirabilis on Banknotes Using 16s rRNA Gene in Khartoum State
title_sort identification of proteus mirabilis on banknotes using 16s rrna gene in khartoum state
topic Proteus mirabilis, banknotes, 16S rRNA, Khartoum State
url https://doi.org/10.18502/sjms.v13i3.2955
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