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      Neonatal listeriosis during a countrywide epidemic in South Africa: A tertiary hospital's experience

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          Abstract

          BACKGROUND. A countrywide epidemic of Listeria monocytogenes (LM) in South Africa began in the first quarter of 2017, rapidly becoming the world's largest LM outbreak to date.METHODS. We describe the clinical course of neonates with culture-confirmed LM infection admitted to a tertiary neonatal unit at Tygerberg Hospital, Cape Town (1 January 2017 - 31 January 2018). Current epidemic LM cases were compared with a historical cohort of sporadic neonatal LM cases at our institution (2006 - 2016). The global literature on epidemic neonatal LM outbreaks (1 January 1978 - 31 December 2017) was reviewed.RESULTS. Twelve neonates (median gestational age 35 weeks, median birth weight 2 020 g) were treated for confirmed LM bacteraemia in 2017/18, presenting at a median age of 0.5 days. In 5 cases, neurolisteriosis was suspected. Three neonates died (25.0%) v. 8/13 neonatal deaths (61.6%) in the sporadic listeriosis cohort (2006 - 2016) (p=0.075). The institution's neonatal LM infection incidence increased significantly in 2017 from a historical rate of 0.17/1 000 live births to 1.4/1 000 (p<0.001). During the current LM epidemic, the crude neonatal fatality rate exceeded the average calculated global epidemic neonatal LM mortality (3/12 (25.0%) v. 50/290 (17.2%); p=0.448). Possible factors contributing to the high mortality rate in this epidemic LM neonatal cohort may include more virulent disease associated with sequence type 6 and the predominance of early-onset disease.CONCLUSIONS. Epidemic neonatal listeriosis at Tygerberg Hospital was associated with a predominance of bacteraemic, early-onset disease. Listeriosis-associated mortality rates were higher than previously published, but lower than the rate in a historical institutional cohort.

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          Listeria monocytogenes lineages: Genomics, evolution, ecology, and phenotypic characteristics.

          Listeria monocytogenes consists of at least 4 evolutionary lineages (I, II, III, and IV) with different but overlapping ecological niches. Most L. monocytogenes isolates seem to belong to lineages I and II, which harbor the serotypes more commonly associated with human clinical cases, including serotype 1/2a (lineage II) and serotypes 1/2b and 4b (lineage I). Lineage II strains are common in foods, seem to be widespread in the natural and farm environments, and are also commonly isolated from animal listeriosis cases and sporadic human clinical cases. Most human listeriosis outbreaks are associated with lineage I isolates though. In addition, a number of studies indicate that, in many countries, lineage I strains are overrepresented among human isolates, as compared to lineage II strains. Lineage III and IV strains on the other hand are rare and predominantly isolated from animal sources. The apparent differences in the distribution of strains representing the L. monocytogenes lineages has lead to a number of studies aimed at identifying phenotypic differences among the different lineages. Interestingly, lineage II isolates seem to carry more plasmids than lineage I isolates and these plasmids often confer resistance to toxic metals and possibly other compounds that may be found in the environment. Moreover, lineage II isolates seem to be more resistant to bacteriocins than lineage I isolates, which probably confers an advantage in environments where bacteriocin-producing organisms are abundant. A large number of lineage II isolates and strains have been shown to be virulence-attenuated due to premature stop codon mutations in inlA and mutations in prfA. A subset of lineage I isolates carry a listeriolysin S hemolysin, which is not present in isolates belonging to lineages II, III, or IV. While lineage II isolates also show higher recombination rates than lineage I isolates, possibly facilitating adaptation of lineage II strains to diverse environments, lineage I isolates are clonal and show a low prevalence of plasmids and IS elements, suggesting that lineage I isolates may have mechanisms that limit the acquisition of foreign DNA by horizontal gene transfer. Diversifying selection has also been shown to have played an important role during evolution of the L. monocytogenes lineages and during divergence of L. monocytogenes from the non-pathogenic species L. innocua. Overall evidence thus suggests that the 4 L. monocytogenes lineages identified so far represent distinct ecologic, genetic, and phenotypic characteristics, which appear to affect their ability to be transmitted through foods and to cause human disease. Further insights into the ecology, evolution, and characteristics of these lineages will thus not only provide an improved understanding of the evolution of this foodborne pathogen, but may also facilitate improved control of foodborne listeriosis. Copyright © 2010 Elsevier GmbH. All rights reserved.
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            Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study

            Listeriosis is a severe foodborne infection and a notifiable disease in France. We did a nationwide prospective study to characterise its clinical features and prognostic factors.
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              Listeria monocytogenes sequence type 6 and increased rate of unfavorable outcome in meningitis: epidemiologic cohort study.

              We analyzed clinical characteristics, treatment, genetic diversity, and outcome of 92 adults with Listeria monocytogenes meningitis included in 2 prospective nationwide cohort studies.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                samj
                SAMJ: South African Medical Journal
                SAMJ, S. Afr. med. j.
                Health and Medical Publishing Group (Cape Town, Western Cape Province, South Africa )
                0256-9574
                2078-5135
                October 2018
                : 108
                : 10
                : 818-827
                Affiliations
                [08] Cape Town orgnameTygerberg Hospital orgdiv1National Health Laboratory Service South Africa
                [06] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Global Health South Africa
                [01] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Paediatrics and Child Health South Africa
                [03] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Paediatrics and Child Health South Africa
                [09] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Science orgdiv2Department of Paediatrics and Child Health South Africa
                [07] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Medical Microbiology South Africa
                [04] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Paediatrics and Child Health South Africa
                [02] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Global Health South Africa
                [05] Cape Town orgnameStellenbosch University orgdiv1Faculty of Medicine and Health Sciences orgdiv2Department of Paediatrics and Child Health South Africa
                Article
                S0256-95742018001100014
                10.7196/samj.2018.v108i10.13207
                30421708
                2bd5d452-6c67-492a-9572-e9fb475be0fc

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

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                Figures: 0, Tables: 0, Equations: 0, References: 35, Pages: 10
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                SciELO South Africa


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