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1.
J Fish Dis ; 42(1): 85-95, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30411368

ABSTRACT

A total of 777 fish from three growing regions of New Zealand Chinook salmon farms comprising of five sites were tested. Quantitative PCR was used to determine the distribution of New Zealand rickettsia-like organism and Tenacibaculum maritimum. Genetic information from these bacteria were then compared with strains reported worldwide. Using this information, suggested associations of pathogens with clinically affected fish were made. NZ-RLO was detected in two of the three regions, and T. maritimum was detected in all regions. Three strains of NZ-RLO were identified during this study. Based on analysis of the ITS rRNA gene, NZ-RLO1 appears to be part of an Australasian grouping sharing high similarity with the Tasmanian RLO, NZ-RLO2 was shown to be the same as an Irish strain, and NZ-RLO3 was shown be closely related to two strains from Chile. Based on multi-locus sequence typing, the New Zealand T. maritimum was the same as Australian strains. NZ-RLOs were detected more frequently in fish with skin ulcers than fish without skin ulcers. While additional research is required to investigate the pathogenicity of these organisms, this is the first time that NZ-RLOs have been associated with the development of clinical infections in farmed Chinook salmon.


Subject(s)
Fish Diseases/microbiology , Flavobacteriaceae Infections/veterinary , Piscirickettsiaceae Infections/veterinary , Piscirickettsiaceae/genetics , Salmon , Tenacibaculum/genetics , Animals , Aquaculture , Genes, rRNA , Multilocus Sequence Typing , New Zealand/epidemiology , Phylogeny , Piscirickettsiaceae Infections/epidemiology , Skin Ulcer/veterinary
2.
Health Aff (Millwood) ; 36(7): 1211-1217, 2017 07 01.
Article in English | MEDLINE | ID: mdl-28679807

ABSTRACT

Although end-of-life medical spending is often viewed as a major component of aggregate medical expenditure, accurate measures of this type of medical spending are scarce. We used detailed health care data for the period 2009-11 from Denmark, England, France, Germany, Japan, the Netherlands, Taiwan, the United States, and the Canadian province of Quebec to measure the composition and magnitude of medical spending in the three years before death. In all nine countries, medical spending at the end of life was high relative to spending at other ages. Spending during the last twelve months of life made up a modest share of aggregate spending, ranging from 8.5 percent in the United States to 11.2 percent in Taiwan, but spending in the last three calendar years of life reached 24.5 percent in Taiwan. This suggests that high aggregate medical spending is due not to last-ditch efforts to save lives but to spending on people with chronic conditions, which are associated with shorter life expectancies.


Subject(s)
Financing, Government/statistics & numerical data , Health Expenditures/statistics & numerical data , Terminal Care/economics , Europe , Global Health , Humans , Japan , North America
3.
Dis Aquat Organ ; 68(1): 1-5, 2005 Dec 30.
Article in English | MEDLINE | ID: mdl-16465828

ABSTRACT

In 1995, and again in 1998, high mortalities of pilchards Sardinops sagax neopilchardus were seen over their entire geographical range on the Australian coastline. A virus with typical herpesvirus morphology was identified as the causative agent, although the source of the virus remains unknown. At the time of the mortality events, the only available diagnostic test available for the detection of the virus was electron microscopy and hence, development of a rapid diagnostic test for detection and identification of the virus was required. Initial sequence data for Pilchard herpesvirus (PHV) was acquired by comparing the highly conserved region of the ORF 62 gene of other piscine herpesviruses (Ictalurid herpesvirus 1 [Channel catfish virus, CCV] and Salmonid herpesvirus 2 [Oncorhynchus masou virus, SaHV2, OMV]), and designing primers that successfully amplified a fragment of PHV. Here we describe the use of polymerase chain reaction (PCR) technology to detect PHV in infected tissues. Sequence analysis of amplified fragment resulting from this PCR is different from all known herpesviruses and can therefore distinguish PHV from all known viruses.


Subject(s)
Disease Outbreaks/veterinary , Fish Diseases/virology , Herpesviridae Infections/veterinary , Herpesviridae/isolation & purification , Polymerase Chain Reaction/veterinary , Animals , Australia/epidemiology , Base Sequence , DNA Primers , Electrophoresis, Agar Gel/veterinary , Endodeoxyribonucleases/genetics , Fish Diseases/mortality , Fishes , Herpesviridae/genetics , Herpesviridae Infections/mortality , Herpesviridae Infections/virology , Molecular Sequence Data , Polymerase Chain Reaction/methods , Sensitivity and Specificity , Sequence Analysis, DNA/veterinary , Viral Proteins/genetics
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