dc.contributor.author | Phiri, Abel F.N.D. | |
dc.contributor.author | Abia, Akebe Luther King | |
dc.contributor.author | Amoako, Daniel Gyamfi | |
dc.contributor.author | Mkakosya, Rajab | |
dc.contributor.author | Sundsfjord, Arnfinn | |
dc.contributor.author | Essack, Sabiha | |
dc.contributor.author | Simonsen, Gunnar Skov | |
dc.date.accessioned | 2021-09-13T08:48:23Z | |
dc.date.available | 2021-09-13T08:48:23Z | |
dc.date.issued | 2021-04-28 | |
dc.description.abstract | Although numerous studies have investigated diarrhoea aetiology in many sub-Saharan African countries, recent data on <i>Shigella</i> species’ involvement in community-acquired acute diarrhoea (CA-AD) in Malawi are scarce. This study investigated the incidence, antibiotic susceptibility profile, genotypic characteristics, and clonal relationships of <i>Shigella flexneri</i> among 243 patients presenting with acute diarrhoea at a District Hospital in Lilongwe, Malawi. <i>Shigella</i> spp. were isolated and identified using standard microbiological and serological methods and confirmed by identifying the <i>ipaH</i> gene using real-time polymerase chain reaction. The isolates’ antibiotic susceptibility to 20 antibiotics was determined using the VITEK 2 system according to EUCAST guidelines. Genes conferring resistance to sulfamethoxazole (<i>sul1</i>, <i>sul2</i> and <i>sul3</i>), trimethoprim (<i>dfrA1</i>, <i>dfrA12</i> and <i>dfrA17</i>) and ampicillin (<i>oxa-1</i> and <i>oxa-2</i>), and virulence genes (<i>ipaBCD, sat, ial, virA, sen, set1A</i> and <i>set1B</i>) were detected by real-time PCR. Clonal relatedness was assessed using ERIC-PCR. Thirty-four <i>Shigella flexneri</i> isolates were isolated (an overall incidence of 14.0%). All the isolates were fully resistant to sulfamethoxazole/trimethoprim (100%) and ampicillin (100%) but susceptible to the other antibiotics tested. The <i>sul1 (79%), sul2 (79%), sul3 (47%), dfrA12 (71%)</i> and <i>dfrA17</i> (56%) sulfonamide and trimethoprim resistance genes were identified; <i>Oxa-1, oxa-2</i> and <i>dfrA1</i> were not detected. The virulence genes <i>ipaBCD (85%), sat (85%), ial (82%), virA (76%), sen (71%), stx (71%), set1A (26%)</i> and <i>set1B</i> (18%) were detected. ERIC-PCR profiling revealed that the Shigella isolates were genetically distinct and clonally unrelated, indicating the potential involvement of genetically distinct <i>S. flexneri</i> in CA-AD in Malawi. The high percentage resistance to ampicillin and sulfamethoxazole/trimethoprim and the presence of several virulence determinants in these isolates emphasises a need for continuous molecular surveillance studies to inform preventive measures and management of <i>Shigella</i>-associated diarrhoeal infections in Malawi. | en_US |
dc.identifier.citation | Phiri, Abia, Amoako, Mkakosya, Sundsfjord, Essack, Simonsen. Burden, antibiotic resistance, and clonality of shigella spp. Implicated in community-acquired acute diarrhoea in Lilongwe, Malawi. Tropical Medicine and Infectious Disease. 2021;6(2) | en_US |
dc.identifier.cristinID | FRIDAID 1918413 | |
dc.identifier.doi | 10.3390/tropicalmed6020063 | |
dc.identifier.issn | 2414-6366 | |
dc.identifier.uri | https://hdl.handle.net/10037/22496 | |
dc.language.iso | eng | en_US |
dc.publisher | MDPI | en_US |
dc.relation.journal | Tropical Medicine and Infectious Disease | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2021 The Author(s) | en_US |
dc.subject | VDP::Medical disciplines: 700 | en_US |
dc.subject | VDP::Medisinske Fag: 700 | en_US |
dc.title | Burden, antibiotic resistance, and clonality of shigella spp. Implicated in community-acquired acute diarrhoea in Lilongwe, Malawi | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |