Pulford Caisey V, Perez-Sepulveda Blanca M, Ingle Danielle J, Bengtsson Rebecca J, Bennett Rebecca J, Rodwell Ella V, Pardos de la Gandara Maria, Chong Charlotte E, De Silva P Malaka, Ravel Magali, Guibert Véronique, Njamkepo Elisabeth, Hall Neil, Chattaway Marie A, Howden Benjamin P, Williamson Deborah A, Hinton Jay C D, Weill François-Xavier, Baker Kate S
Clinical Infection, Microbiology, and Immunology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Department of Microbiology and Immunology, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Lancet Microbe. 2025 Jul 25:101150. doi: 10.1016/j.lanmic.2025.101150.
Non-typhoidal Salmonella is a globally important bacterial pathogen, typically associated with foodborne gastrointestinal infection. Some non-typhoidal Salmonella serovars can also colonise typically sterile sites in people to cause invasive non-typhoidal Salmonella disease. Salmonella enterica serovar Panama is responsible for a substantial number of cases of human bloodstream infection, but despite its global dissemination, numerous outbreaks, and a reported association with invasive non-typhoidal Salmonella disease, S enterica serovar Panama (S Panama) is understudied. We aimed to describe the genomic epidemiology and evolutionary history of S Panama to provide a vital baseline of understanding for this globally important serovar.
In this genomic epidemiology study, we analysed S Panama genomes derived from historical collections, national surveillance datasets, and publicly available epidemiological and whole-genome sequencing data which span the years 1931-2019. Maximum likelihood and Bayesian phylodynamic approaches were used to investigate population structure and evolutionary history and to infer geotemporal dissemination. A combination of different bioinformatic approaches with short-read and long-read data were used to characterise geographical and clade-specific trends in antimicrobial resistance (AMR) and genetic markers for invasiveness.
We analysed 836 S Panama genomes, of which 559 (67%) were sequenced as part of this study. The collection represents all inhabited continents and includes isolates collected between 1931 and 2019. We identified the presence of four geographically linked S Panama clades (C1 [ie, the Latin America and the Caribbean clade; n=338], C2 [ie, the European clade; n=124], C3 [ie, the Martinique clade; n=131], and C4 [ie, the Asia and Oceania clade; n=104]) and regional trends in AMR profiles. Most isolates (715 [86%] of 836) were pan-susceptible to antibiotics and belonged to clades circulating in Latin America and the Caribbean (64%, n=458). Most antibiotic-resistant isolates in our collection (113 [93%] of 121) fell within clades C4 (ie, the Asia and Oceania clade) and C2 (ie, the European clade), the latter of which had the highest invasiveness index values based on the conservation of 196 extraintestinal predictor genes.
This first large-scale phylogenetic analysis of S Panama has revealed important information about the population structure, AMR, global ecology, and genetic markers of invasiveness of the identified genomic subtypes. Our findings provide an important baseline for understanding S Panama infection. The presence of multidrug-resistant clades with elevated invasiveness index values should be monitored through ongoing surveillance, as such clades could pose an increased public health risk.
UK Research and Innovation Global Challenges Research Fund and Biotechnology and Biological Sciences Research Council, UK Medical Research Council, Wellcome Trust, John Lennon Memorial Scholarship, Institut Pasteur, Santé publique France, Fondation Le Roch-Les Mousquetaires, Investissement d'Avenir Programme, and Australian National Health and Medical Research Council.
非伤寒沙门氏菌是一种在全球范围内具有重要意义的细菌病原体,通常与食源性胃肠道感染有关。一些非伤寒沙门氏菌血清型也可在人体通常无菌的部位定植,从而导致侵袭性非伤寒沙门氏菌病。肠炎沙门氏菌巴拿马血清型导致了大量人类血流感染病例,但尽管其在全球传播、多次爆发疫情,且有报道称其与侵袭性非伤寒沙门氏菌病有关,但对肠炎沙门氏菌巴拿马血清型(S巴拿马)的研究仍不足。我们旨在描述S巴拿马的基因组流行病学和进化史,为这种在全球具有重要意义的血清型提供至关重要的理解基线。
在这项基因组流行病学研究中,我们分析了来自历史馆藏、国家监测数据集以及公开可得的流行病学和全基因组测序数据(时间跨度为1931年至2019年)中的S巴拿马基因组。使用最大似然法和贝叶斯系统发育动力学方法来研究种群结构和进化史,并推断地理时间传播情况。结合不同的生物信息学方法以及短读长和长读长数据,以表征抗菌药物耐药性(AMR)的地理和分支特异性趋势以及侵袭性的遗传标记。
我们分析了836个S巴拿马基因组,其中559个(67%)是本研究测序的。该样本涵盖了所有有人居住的大陆,包括1931年至2019年期间收集的分离株。我们确定存在四个地理相关的S巴拿马分支(C1[即拉丁美洲和加勒比分支;n = 338]、C2[即欧洲分支;n = 124]、C3[即马提尼克分支;n = 131]和C4[即亚洲和大洋洲分支;n = 104])以及AMR谱的区域趋势。大多数分离株(836个中的715个[86%])对多种抗生素敏感,属于在拉丁美洲和加勒比地区传播的分支(6