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Dive into the research topics where Dominic E. Dwyer is active.

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Featured researches published by Dominic E. Dwyer.


Science | 1995

Genomic Structure of an Attenuated Quasi Species of HIV-1 from a Blood Transfusion Donor and Recipients

Nicholas J. Deacon; A. Tsykin; Ajantha Solomon; K. Smith; M. Ludford-Menting; David J. Hooker; Dale A. McPhee; Alison L. Greenway; Anne Ellett; Catherine Chatfield; Victoria A. Lawson; Suzanne M. Crowe; Anne L. Maerz; Secondo Sonza; Jenny Learmont; John S. Sullivan; Anthony L. Cunningham; Dominic E. Dwyer; D. Dowton; John Mills

A blood donor infected with human immunodeficiency virus-type 1 (HIV-1) and a cohort of six blood or blood product recipients infected from this donor remain free of HIV-1-related disease with stable and normal CD4 lymphocyte counts 10 to 14 years after infection. HIV-1 sequences from either virus isolates or patient peripheral blood mononuclear cells had similar deletions in the nef gene and in the region of overlap of nef and the U3 region of the long terminal repeat (LTR). Full-length sequencing of one isolate genome and amplification of selected HIV-1 genome regions from other cohort members revealed no other abnormalities of obvious functional significance. These data show that survival after HIV infection can be determined by the HIV genome and support the importance of nef or the U3 region of the LTR in determining the pathogenicity of HIV-1.


Antiviral Research | 2009

Emergence and spread of oseltamivir-resistant A(H1N1) influenza viruses in Oceania, South East Asia and South Africa

Aeron C. Hurt; Joanne Ernest; Yi-Mo Deng; Pina Iannello; Terry G. Besselaar; Chris Birch; Philippe Buchy; Malinee Chittaganpitch; Shu-Chun Chiu; Dominic E. Dwyer; Aurélie Guigon; Bruce Harrower; Ip Peng Kei; Tuckweng Kok; Cui Lin; Ken McPhie; Apandi Mohd; Remigio M. Olveda; Tony Panayotou; William D. Rawlinson; Lesley Scott; David W. Smith; Holly D'Souza; Naomi Komadina; Robert D. Shaw; Anne Kelso; Ian G. Barr

The neuraminidase inhibitors (NAIs) are an effective class of antiviral drugs for the treatment of influenza A and B infections. Until recently, only a low prevalence of NAI resistance (<1%) had been detected in circulating viruses. However, surveillance in Europe in late 2007 revealed significant numbers of A(H1N1) influenza strains with a H274Y neuraminidase mutation that were highly resistant to the NAI oseltamivir. We examined 264 A(H1N1) viruses collected in 2008 from South Africa, Oceania and SE Asia for their susceptibility to NAIs oseltamivir, zanamivir and peramivir in a fluorescence-based neuraminidase inhibition assay. Viruses with reduced oseltamivir susceptibility were further analysed by pyrosequencing assay. The frequency of the oseltamivir-resistant H274Y mutant increased significantly after May 2008, resulting in an overall proportion of 64% (168/264) resistance among A(H1N1) strains, although this subtype represented only 11.6% of all isolates received during 2008. H274Y mutant viruses demonstrated on average a 1466-fold reduction in oseltamivir susceptibility and 527-fold reduction in peramivir sensitivity compared to wild-type A(H1N1) viruses. The mutation had no impact on zanamivir susceptibility. Ongoing surveillance is essential to monitor how these strains may spread or persist in the future and to evaluate the effectiveness of treatments against them.


Clinical Microbiology Reviews | 2012

Bed Bugs: Clinical Relevance and Control Options

Stephen L. Doggett; Dominic E. Dwyer; Pablo F. Peñas; Richard C. Russell

SUMMARY Since the late 1990s, bed bugs of the species Cimex lectularius and Cimex hemipterus have undergone a worldwide resurgence. These bed bugs are blood-sucking insects that readily bite humans. Cutaneous reactions may occur and can start out as small macular lesions that can develop into distinctive wheals of around 5 cm in diameter, which are accompanied by intense itching. Occasionally, bullous eruptions may result. If bed bugs are numerous, the patient can present with widespread urticaria or eythematous rashes. Often, bites occur in lines along the limbs. Over 40 pathogens have been detected in bed bugs, but there is no definitive evidence that they transmit any disease-causing organisms to humans. Anemia may result when bed bugs are numerous, and their allergens can trigger asthmatic reactions. The misuse of chemicals and other technologies for controlling bed bugs has the potential to have a deleterious impact on human health, while the insect itself can be the cause of significant psychological trauma. The control of bed bugs is challenging and should encompass a multidisciplinary approach utilizing nonchemical means of control and the judicious use of insecticides. For accommodation providers, risk management procedures should be implemented to reduce the potential of bed bug infestations.


Microbes and Infection | 2000

Arboviruses associated with human disease in Australia.

Richard C. Russell; Dominic E. Dwyer

Mosquito-borne arboviruses are an important public health issue in Australia. The alphaviruses Ross River and Barmah Forest virus are widespread and active annually, and cause debilitating polyarthritis. The flaviviruses Murray Valley encephalitis, Kunjin and Japanese encephalitis virus are restricted in distribution and activity but may cause life-threatening illness, and dengue viruses are active in some areas.


Emerging Infectious Diseases | 2012

Influenza Virus A (H10N7) in Chickens and Poultry Abattoir Workers, Australia

George G. Arzey; Peter D. Kirkland; K. Edla Arzey; Melinda J. Frost; Patrick Maywood; Stephen Conaty; Aeron C. Hurt; Yi-Mo Deng; Pina Iannello; Ian G. Barr; Dominic E. Dwyer; V. Mala Ratnamohan; Kenneth McPhie; Paul Selleck

In March 2010, an outbreak of low pathogenicity avian influenza A (H10N7) occurred on a chicken farm in Australia. After processing clinically normal birds from the farm, 7 abattoir workers reported conjunctivitis and minor upper respiratory tract symptoms. Influenza virus A subtype H10 infection was detected in 2 workers.


The Journal of Infectious Diseases | 2012

Characteristics of a widespread community cluster of H275Y oseltamivir-resistant A(H1N1)pdm09 influenza in Australia

Aeron C. Hurt; Kate Hardie; Noelene Wilson; Yi-Mo Deng; Maggi Osbourn; Sook-Kwan Leang; Raphael Tc Lee; Pina Iannello; N. Gehrig; R. Shaw; Peter Wark; Natalie Caldwell; R. Givney; L. Xue; Sebastian Maurer-Stroh; Dominic E. Dwyer; Bing Wang; David W. Smith; Avram Levy; Robert Booy; R. Dixit; Tony Merritt; Anne Kelso; Craig Dalton; David N. Durrheim; Ian G. Barr

Background. Oseltamivir resistance in A(H1N1)pdm09 influenza is rare, particularly in untreated community cases. Sustained community transmission has not previously been reported. Methods. Influenza specimens from the Asia–Pacific region were collected through sentinel surveillance, hospital, and general practitioner networks. Clinical and epidemiological information was collected on patients infected with oseltamivir-resistant viruses. Results. Twenty-nine (15%) of 191 A(H1N1)pdm09 viruses collected between May and September 2011 from Hunter New England (HNE), Australia, contained the H275Y neuraminidase substitution responsible for oseltamivir resistance. Only 1 patient had received oseltamivir before specimen collection. The resistant strains were genetically very closely related, suggesting the spread of a single variant. Ninety percent of cases lived within 50 kilometers. Three genetically similar oseltamivir-resistant variants were detected outside of HNE, including 1 strain from Perth, approximately 4000 kilometers away. Computational analysis predicted that neuraminidase substitutions V241I, N369K, and N386S in these viruses may offset the destabilizing effect of the H275Y substitution. Conclusions This cluster represents the first widespread community transmission of H275Y oseltamivir-resistant A(H1N1)pdm09 influenza. These cases and data on potential permissive mutations suggest that currently circulating A(H1N1)pdm09 viruses retain viral fitness in the presence of the H275Y mutation and that widespread emergence of oseltamivir-resistant strains may now be more likely.


Emerging Infectious Diseases | 2010

Oseltamivir resistance in adult oncology and hematology patients infected with pandemic (H1N1) 2009 virus, Australia.

Adrian R Tramontana; B George; Aeron C. Hurt; Joseph S. Doyle; Katherine M Langan; Alistair B. Reid; Janet M. Harper; Karin Thursky; Leon J. Worth; Dominic E. Dwyer; C. Orla Morrissey; Paul D. R. Johnson; Kirsty Buising; Simon J. Harrison; John F. Seymour; Patricia E. Ferguson; Bin Wang; Justin T. Denholm; Allen C. Cheng; Monica A. Slavin

Resistance in virus-infected stem cell transplant recipients illustrates the need for surveillance.


Journal of Virology | 2004

Role of Minority Populations of Human Immunodeficiency Virus Type 1 in the Evolution of Viral Resistance to Protease Inhibitors

Charlotte Charpentier; Dominic E. Dwyer; Fabrizio Mammano; Denise Lecossier; François Clavel; Allan J. Hance

ABSTRACT Human immunodeficiency virus type 1 (HIV-1) drug resistance results from the accumulation of mutations in the viral genes targeted by the drugs. These genetic changes, however, are commonly detected and monitored by techniques that only take into account the dominant population of plasma virus. Because HIV-1-infected patients harbor a complex and diverse mixture of virus populations, the mechanisms underlying the emergence and the evolution of resistance are not fully elucidated. Using techniques that allow the quantification of resistance mutations in minority virus species, we have monitored the evolution of resistance in plasma virus populations from patients failing protease inhibitor treatment. Minority populations with distinct resistance genotypes were detected in all patients throughout the evolution of resistance. The emergence of new dominant genotypes followed two possible mechanisms: (i) emergence of a new mutation in a currently dominant genotype and (ii) emergence of a new genotype derived from a minority virus species. In most cases, these population changes were associated with an increase in resistance at the expense of a reduction in replication capacity. Our findings provide a preliminary indication that minority viral species, which evolve independently of the majority virus population, can eventually become dominant populations, thereby serving as a reservoir of diversity and possibly accelerating the development of drug resistance.


Journal of Clinical Microbiology | 2010

Comparison of a Rapid Antigen Test with Nucleic Acid Testing during Cocirculation of Pandemic Influenza A/H1N1 2009 and Seasonal Influenza A/H3N2

Jen Kok; Christopher C. Blyth; Hong Foo; Jason Patterson; Janette Taylor; Kenneth McPhie; V. Mala Ratnamohan; Jonathan R. Iredell; Dominic E. Dwyer

ABSTRACT The rapid diagnosis of influenza is critical in optimizing clinical management. Rapid antigen tests have decreased sensitivity in detecting pandemic influenza A/H1N1 2009 virus compared to seasonal influenza A subtypes (53.4% versus 74.2%, P < 0.001). Nucleic acid tests should be used to detect pandemic influenza virus when rapid antigen tests are negative.


Journal of Clinical Microbiology | 2005

Rapid and Sensitive Detection of Severe Acute Respiratory Syndrome Coronavirus by Rolling Circle Amplification

Bin Wang; Simon J. Potter; Yiguang Lin; Anthony L. Cunningham; Dominic E. Dwyer; Yuelong Su; Xuejun Ma; Yunde Hou; Nitin K. Saksena

ABSTRACT The severe acute respiratory syndrome (SARS) epidemic of 2003 was responsible for 774 deaths and caused significant economic damage worldwide. Since July 2003, a number of SARS cases have occurred in China, raising the possibility of future epidemics. We describe here a rapid, sensitive, and highly efficient assay for the detection of SARS coronavirus (SARS-CoV) in cultured material and a small number (n = 7) of clinical samples. Using rolling circle amplification (RCA), we were able to achieve sensitive detection levels of SARS-CoV RNA in both solid and liquid phases. The main advantage of RCA is that it can be performed under isothermal conditions with minimal reagents and avoids the generation of false-positive results, a problem that is frequently encountered in PCR-based assays. Furthermore, the RCA technology provides a faster, more sensitive, and economical option to currently available PCR-based methods.

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Jen Kok

University of Sydney

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Holly Seale

University of New South Wales

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Bin Wang

University of New South Wales

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Christopher C. Blyth

University of Western Australia

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C. Raina MacIntyre

University of New South Wales

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C.R. MacIntyre

University of New South Wales

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