Georgina S. E. Rimmer
Centre for Environment, Fisheries and Aquaculture Science
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Publication
Featured researches published by Georgina S. E. Rimmer.
Heredity | 2010
Ross Houston; Chris Haley; Alastair Hamilton; Derrick R Guy; J. C. Mota-Velasco; Almas Gheyas; A. E. Tinch; John B. Taggart; James E. Bron; William G. Starkey; Brendan McAndrew; David W. Verner-Jeffreys; Richard Paley; Georgina S. E. Rimmer; I. Tew; S. C. Bishop
Infectious pancreatic necrosis (IPN) is a viral disease with a significant negative impact on the global aquaculture of Atlantic salmon. IPN outbreaks can occur during specific windows of both the freshwater and seawater stages of the salmon life cycle. Previous research has shown that a proportion of the variation seen in resistance to IPN is because of host genetics, and we have shown that major quantitative trait loci (QTL) affect IPN resistance at the seawater stage of production. In the current study, we completed a large freshwater IPN challenge experiment to allow us to undertake a thorough investigation of the genetic basis of resistance to IPN in salmon fry, with a focus on previously identified QTL regions. The heritability of freshwater IPN resistance was estimated to be 0.26 on the observed scale and 0.55 on the underlying scale. Our results suggest that a single QTL on linkage group 21 explains almost all the genetic variation in IPN mortality under our experimental conditions. A striking contrast in mortality is seen between fry classified as homozygous susceptible versus homozygous resistant, with QTL-resistant fish showing virtually complete resistance to IPN mortality. The findings highlight the importance of the major QTL in the genetic regulation of IPN resistance across distinct physiological lifecycle stages, environmental conditions and viral isolates. These results have clear scientific and practical implications for the control of IPN.
PLOS ONE | 2009
David W. Verner-Jeffreys; Timothy J. Welch; Tamar Schwarz; Michelle J. Pond; Martin J. Woodward; Sarah J. Haig; Georgina S. E. Rimmer; Edward Roberts; Victoria Morrison; Craig Baker-Austin
Background Antimicrobials are used to directly control bacterial infections in pet (ornamental) fish and are routinely added to the water these fish are shipped in to suppress the growth of potential pathogens during transport. Methodology/Principal Findings To assess the potential effects of this sustained selection pressure, 127 Aeromonas spp. isolated from warm and cold water ornamental fish species were screened for tolerance to 34 antimicrobials. Representative isolates were also examined for the presence of 54 resistance genes by a combination of miniaturized microarray and conventional PCR. Forty-seven of 94 Aeromonas spp. isolates recovered from tropical ornamental fish and their carriage water were tolerant to ≥15 antibiotics, representing seven or more different classes of antimicrobial. The quinolone and fluoroquinolone resistance gene, qnrS2, was detected at high frequency (37% tested recent isolates were positive by PCR). Class 1 integrons, IncA/C broad host range plasmids and a range of other antibiotic resistance genes, including floR, bla TEM−1, tet(A), tet(D), tet(E), qacE2, sul1, and a number of different dihydrofolate reductase and aminoglycoside transferase coding genes were also detected in carriage water samples and bacterial isolates. Conclusions These data suggest that ornamental fish and their carriage water act as a reservoir for both multi-resistant bacteria and resistance genes.
Emerging Infectious Diseases | 2012
David W. Verner-Jeffreys; Craig Baker-Austin; Michelle J. Pond; Georgina S. E. Rimmer; R. Kerr; David M. Stone; Rachael Griffin; Peter White; Nicholas Stinton; Kevin Denham; James A. Leigh; Nicola Jones; Matthew Longshaw; Stephen W. Feist
“Doctor” fish might not be such good doctors after all. These fish are used for the increasingly popular spa treatment called fish pedicures. During these sessions, spa patrons immerse their feet in water, allowing the live fish to feed on dead skin, mainly for cosmetic reasons. However, examinations of doctor fish destined for these spas found that they can carry harmful bacteria. Thus, although reports of human infection after fish pedicures are few, there may be some risks. Spa patrons who have underlying medical conditions (such as diabetes, immunosuppression, or even simple breaks in the skin) are already discouraged from taking such treatments. However, spas that offer fish pedicures should also consider using only disease-free fish reared in controlled facilities under high standards of husbandry and welfare.
PLOS ONE | 2016
Irene Cano; David W. Verner-Jeffreys; Ronny van Aerle; Richard Paley; Edmund J. Peeler; Matthew Green; Georgina S. E. Rimmer; Jacqueline Savage; C Joiner; Amanda Bayley; Jason Mewett; Jonathan Hulland; Stephen W. Feist
The transmission of puffy skin disease (PSD) to rainbow trout Oncorhynchus mykiss Walbaum was tested in the laboratory by conducting co-habitation challenges with puffy skin (PS)-affected fish (Trojans) collected from the field. Two separate challenges were conducted using Trojans sourced from two different sites and diploid (first trial) or triploid (second trial) naïve fish. PSD-specific clinical signs were observed in both groups of naïve fish, with 66% of the fish sampled during the challenges showing signs of varying severity. The first clinical features of PSD were presented as white oval skin patches on one or both flanks 15–21 days post-challenge (dpc). The extent of the lesions ranged from 10 to 90% of the body surface, depending on the severity of the lesion. Both the severity and number of affected fish increased during the challenge. Macroscopically, oedema of the skin and multifocal petechial haemorrhaging were observed towards the end of the trials. Abnormal fish behaviour consisting of “flashing” and excessive mucous production was noted from 15 dpc onwards. Fish with severe PSD lesions also displayed inappetence and associated emaciation. Rodlet cells were observed in 41% of the fresh skin scrapes analysed from the second trial. Histologically epidermal oedema was observed in 31% of the naive fish showing gross pathology, with additional 12% displaying epidermal hyperplasia, mostly observed at the end of the challenge. Other concomitant features of the PSD lesions in challenged fish were epithelial erosion and sloughing, and occasionally mild or focal inflammation. No consistent pathology of internal organs was observed. The parasites Ichthyophthirius multifiliis and Ichthyobodo necator were observed in skin samples of a proportion of naïve challenged fish and in Trojans but not in control fish. The presence of these and other known fish pathogens in the skin of PSD-fish was confirmed by high-throughput sequencing analysis. In summary, we have demonstrated that PSD is a transmissible condition. However, even though a number of known fish pathogens were identified in the skin tissues of PSD-fish, the actual causative infectious agent(s) remain(s) unknown.
Applied and Environmental Microbiology | 2017
Irene Cano; Ronny van Aerle; Stuart Ross; David W. Verner-Jeffreys; Richard Paley; Georgina S. E. Rimmer; David Ryder; Patrick Hooper; David A. Stone; Stephen W. Feist
ABSTRACT One of the fastest growing fisheries in the UK is the king scallop (Pecten maximus L.), also currently rated as the second most valuable fishery. Mass mortality events in scallops have been reported worldwide, often with the causative agent(s) remaining uncharacterized. In May 2013 and 2014, two mass mortality events affecting king scallops were recorded in the Lyme Bay marine protected area (MPA) in Southwest England. Histopathological examination showed gill epithelial tissues infected with intracellular microcolonies (IMCs) of bacteria resembling Rickettsia-like organisms (RLOs), often with bacteria released in vascular spaces. Large colonies were associated with cellular and tissue disruption of the gills. Ultrastructural examination confirmed the intracellular location of these organisms in affected epithelial cells. The 16S rRNA gene sequences of the putative IMCs obtained from infected king scallop gill samples, collected from both mortality events, were identical and had a 99.4% identity to 16S rRNA gene sequences obtained from “Candidatus Endonucleobacter bathymodioli” and 95% with Endozoicomonas species. In situ hybridization assays using 16S rRNA gene probes confirmed the presence of the sequenced IMC gene in the gill tissues. Additional DNA sequences of the bacterium were obtained using high-throughput (Illumina) sequencing, and bioinformatic analysis identified over 1,000 genes with high similarity to protein sequences from Endozoicomonas spp. (ranging from 77 to 87% identity). Specific PCR assays were developed and applied to screen for the presence of IMC 16S rRNA gene sequences in king scallop gill tissues collected at the Lyme Bay MPA during 2015 and 2016. There was 100% prevalence of the IMCs in these gill tissues, and the 16S rRNA gene sequences identified were identical to the sequence found during the previous mortality event. IMPORTANCE Molluscan mass mortalities associated with IMCs have been reported worldwide for many years; however, apart from histological and ultrastructural characterization, characterization of the etiological agents is limited. In the present work, we provide detailed molecular characterization of an Endozoicomonas-like organism (ELO) associated with an important commercial scallop species.
BMC Genomics | 2016
Diego Robledo; John B. Taggart; Jacqueline Ireland; Brendan McAndrew; William G. Starkey; Chris Haley; Alastair Hamilton; Derrick R Guy; J. C. Mota-Velasco; Almas Gheyas; A. E. Tinch; David W. Verner-Jeffreys; Richard Paley; Georgina S. E. Rimmer; Ian J. Tew; Stephen Bishop; James E. Bron; Ross Houston
Journal of Fish Diseases | 2015
Irene Cano; C Joiner; Amanda Bayley; Georgina S. E. Rimmer; K Bateman; S. W. Feist; David M. Stone; Richard Paley
Journal of Fish Diseases | 2018
Hannah J. Tidbury; C Joiner; Georgina S. E. Rimmer; Holly V. Potter; Nick G. H. Taylor
Archive | 2011
Ross Houston; Stephen Bishop; Chris Haley; James E. Bron; John B. Taggart; Brendan McAndrew; William G. Starkey; Alastair Hamilton; Derrick R Guy; J. C. Mota-Velasco; Almas Gheyas; A. E. Tinch; David W. Verner-Jeffreys; Richard Paley; Georgina S. E. Rimmer; I. Tew
Genomics in Aquaculture International Symposium | 2009
Ross Houston; Chris Haley; Almas Gheyas; Derrick R Guy; Alastair Hamilton; J. C. Mota-Velasco; A. E. Tinch; James E. Bron; Jacqueline Ireland; Brendan McAndrew; William G. Starkey; John B. Taggart; Richard Paley; Georgina S. E. Rimmer; I. Tew; David W. Verner-Jeffreys; Stephen Bishop