TY - JOUR
T1 - Genomic insights into the 2022–2023Vibrio cholerae outbreak in Malawi
AU - Chaguza, Chrispin
AU - Chibwe, Innocent
AU - Chaima, David
AU - Musicha, Patrick
AU - Ndeketa, Latif
AU - Kasambara, Watipaso
AU - Mhango, Chimwemwe
AU - Mseka, Upendo L.
AU - Bitilinyu-Bangoh, Joseph
AU - Mvula, Bernard
AU - Kipandula, Wakisa
AU - Bonongwe, Patrick
AU - Munthali, Richard J.
AU - Ngwira, Selemani
AU - Mwendera, Chikondi A.
AU - Kalizang’oma, Akuzike
AU - Jambo, Kondwani C.
AU - Kambalame, Dzinkambani
AU - Kamng’ona, Arox W.
AU - Steele, A. Duncan
AU - Chauma-Mwale, Annie
AU - Hungerford, Daniel
AU - Kagoli, Matthew
AU - Nyaga, Martin M.
AU - Dube, Queen
AU - French, Neil
AU - Msefula, Chisomo L.
AU - Cunliffe, Nigel A.
AU - Jere, Khuzwayo C.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Malawi experienced its deadliest Vibrio cholerae (Vc) outbreak following devastating cyclones, with >58,000 cases and >1700 deaths reported between March 2022 and May 2023. Here, we use population genomics to investigate the attributes and origin of the Malawi 2022–2023 Vc outbreak isolates. Our results demonstrate the predominance of ST69 clone, also known as the seventh cholera pandemic El Tor (7PET) lineage, expressing O1 Ogawa (~ 80%) serotype followed by Inaba (~ 16%) and sporadic non-O1/non-7PET serogroups (~ 4%). Phylogenetic reconstruction revealed that the Malawi outbreak strains correspond to a recent importation from Asia into Africa (sublineage AFR15). These isolates harboured known antimicrobial resistance and virulence elements, notably the ICEGEN/ICEVchHai1/ICEVchind5 SXT/R391-like integrative conjugative elements and a CTXφ prophage with the ctxB7 genotype compared to historical Malawian Vc isolates. These data suggest that the devastating cyclones coupled with the recent importation of 7PET serogroup O1 strains, may explain the magnitude of the 2022–2023 cholera outbreak in Malawi.
AB - Malawi experienced its deadliest Vibrio cholerae (Vc) outbreak following devastating cyclones, with >58,000 cases and >1700 deaths reported between March 2022 and May 2023. Here, we use population genomics to investigate the attributes and origin of the Malawi 2022–2023 Vc outbreak isolates. Our results demonstrate the predominance of ST69 clone, also known as the seventh cholera pandemic El Tor (7PET) lineage, expressing O1 Ogawa (~ 80%) serotype followed by Inaba (~ 16%) and sporadic non-O1/non-7PET serogroups (~ 4%). Phylogenetic reconstruction revealed that the Malawi outbreak strains correspond to a recent importation from Asia into Africa (sublineage AFR15). These isolates harboured known antimicrobial resistance and virulence elements, notably the ICEGEN/ICEVchHai1/ICEVchind5 SXT/R391-like integrative conjugative elements and a CTXφ prophage with the ctxB7 genotype compared to historical Malawian Vc isolates. These data suggest that the devastating cyclones coupled with the recent importation of 7PET serogroup O1 strains, may explain the magnitude of the 2022–2023 cholera outbreak in Malawi.
UR - http://www.scopus.com/inward/record.url?scp=85199764271&partnerID=8YFLogxK
U2 - 10.1038/s41467-024-50484-w
DO - 10.1038/s41467-024-50484-w
M3 - Article
C2 - 39060226
AN - SCOPUS:85199764271
SN - 2041-1723
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6291
ER -