Ernest C. J. Seamark
University of Pretoria
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Featured researches published by Ernest C. J. Seamark.
PLOS ONE | 2016
Muriel Dietrich; Mabotse A. Tjale; Jacqueline Weyer; Teresa Kearney; Ernest C. J. Seamark; Louis Hendrik Nel; Ara Monadjem; Wanda Markotter
In addition to several emerging viruses, bats have been reported to host multiple bacteria but their zoonotic threats remain poorly understood, especially in Africa where the diversity of bats is important. Here, we investigated the presence and diversity of Bartonella and Rickettsia spp. in bats and their ectoparasites (Diptera and Siphonaptera) collected across South Africa and Swaziland. We collected 384 blood samples and 14 ectoparasites across 29 different bat species and found positive samples in four insectivorous and two frugivorous bat species, as well as their Nycteribiidae flies. Phylogenetic analyses revealed diverse Bartonella genotypes and one main group of Rickettsia, distinct from those previously reported in bats and their ectoparasites, and for some closely related to human pathogens. Our results suggest a differential pattern of host specificity depending on bat species. Bartonella spp. identified in bat flies and blood were identical supporting that bat flies may serve as vectors. Our results represent the first report of bat-borne Bartonella and Rickettsia spp. in these countries and highlight the potential role of bats as reservoirs of human bacterial pathogens.
Fems Microbiology Letters | 2017
Muriel Dietrich; Teresa Kearney; Ernest C. J. Seamark; Wanda Markotter
&NA; Animal‐associated microbiotas form complex communities, which play crucial functions for their host, including susceptibility to infections. Despite increasing attention to bats as reservoirs of zoonotic pathogens, their microbiota is poorly documented, especially for samples potentially implicated in pathogen transmission such as urine and saliva. Here, using low‐biomass individual samples, we examined the composition and structure of bacterial communities excreted by insectivorous bats, focusing on three body habitats (saliva, urine and faeces). We show that niche specialisation occurs as bacterial community composition was distinct across body habitats with the majority of phylotypes being body habitat specific. Our results suggest that urine harbours more diverse bacterial communities than saliva and faeces and reveal potentially zoonotic bacteria such as Leptospira, Rickettsia, Bartonella and Coxiella in all body habitats. Our study emphasised that, in addition to the traditional use of gut‐associated samples such as faeces, both urine and saliva are also of interest because of their diverse microbiota and the potential transmission of pathogenic bacteria. Our results represent a critical baseline for future studies investigating the interactions between microbiota and infection dynamics in bats.
PLOS ONE | 2018
Marike Geldenhuys; Marinda Mortlock; Jacqueline Weyer; K.I.O. Bezuidt; Ernest C. J. Seamark; Teresa Kearney; Cheryl D. Gleasner; Tracy Erkkila; Helen H. Cui; Wanda Markotter
Species within the Neoromicia bat genus are abundant and widely distributed in Africa. It is common for these insectivorous bats to roost in anthropogenic structures in urban regions. Additionally, Neoromicia capensis have previously been identified as potential hosts for Middle East respiratory syndrome (MERS)-related coronaviruses. This study aimed to ascertain the gastrointestinal virome of these bats, as viruses excreted in fecal material or which may be replicating in rectal or intestinal tissues have the greatest opportunities of coming into contact with other hosts. Samples were collected in five regions of South Africa over eight years. Initial virome composition was determined by viral metagenomic sequencing by pooling samples and enriching for viral particles. Libraries were sequenced on the Illumina MiSeq and NextSeq500 platforms, producing a combined 37 million reads. Bioinformatics analysis of the high throughput sequencing data detected the full genome of a novel species of the Circoviridae family, and also identified sequence data from the Adenoviridae, Coronaviridae, Herpesviridae, Parvoviridae, Papillomaviridae, Phenuiviridae, and Picornaviridae families. Metagenomic sequencing data was insufficient to determine the viral diversity of certain families due to the fragmented coverage of genomes and lack of suitable sequencing depth, as some viruses were detected from the analysis of reads-data only. Follow up conventional PCR assays targeting conserved gene regions for the Adenoviridae, Coronaviridae, and Herpesviridae families were used to confirm metagenomic data and generate additional sequences to determine genetic diversity. The complete coding genome of a MERS-related coronavirus was recovered with additional amplicon sequencing on the MiSeq platform. The new genome shared 97.2% overall nucleotide identity to a previous Neoromicia-associated MERS-related virus, also from South Africa. Conventional PCR analysis detected diverse adenovirus and herpesvirus sequences that were widespread throughout Neoromicia populations in South Africa. Furthermore, similar adenovirus sequences were detected within these populations throughout several years. With the exception of the coronaviruses, the study represents the first report of sequence data from several viral families within a Southern African insectivorous bat genus; highlighting the need for continued investigations in this regard.
Mammalia | 2017
Teresa Kearney; Mark Keith; Ernest C. J. Seamark
Abstract Eight bat species were recorded at Gatkop Cave, in the northern part of South Africa in December 2011 (Cloeotis percivali, Hipposideros caffer, Myotis tricolor, Miniopterus natalensis, Nycteris thebaica, Rhinolophus blasii, Rhinolophus smithersi, and Rhinolophus simulator). With the exception of M. natalensis, R. simulator and Myo. tricolor, the other five species were recorded for the first time at Gatkop Cave during this time of the year, when thousands of M. natalensis use the cave as a maternity and nursery roost. Previously it was suggested the large numbers of M. natalensis using Gatkop Cave during the maternal period excluded other bat species. The reason for this recorded change in species roost composition at Gatkop Cave during the maternal period in relation to previous records made from the late 1960s and the mid 1980s is not clear, two possible reasons are the loss of other roosts, or these species were previously present but were not captured as a result of the particular methods used.
Archive | 2007
Victor Van Cakenberghe; Ernest C. J. Seamark
Annals of the Transvaal Museum. - Pretoria | 2008
Teresa Kearney; Victor Van Cakenberghe; Ernest C. J. Seamark; Captain Ndhlovu; Lientjie Cohen
Annals of the Transvaal Museum | 2008
Teresa Kearney; Victor Van Cakenberghe; Ernest C. J. Seamark; Captain Ndhlovu; Lientjie Cohen
Annals of the Transvaal Museum | 2005
Teresa Kearney; Ernest C. J. Seamark
Archive | 2018
Muriel Dietrich; Teresa Kearney; Ernest C. J. Seamark; Janusz Paweska; Wanda Markotter
European journal of taxonomy | 2017
Victor Van Cakenberghe; Guy-Crispin Gembu Tungaluna; Prescott Musaba Akawa; Ernest C. J. Seamark; Erik Verheyen