Towards understanding the liver fluke transmission dynamics on farms: Detection of liver fluke transmitting snail and liver fluke-specific environmental DNA in water samples from an irrigated dairy farm in Southeast Australia
被引:15
|
作者:
论文数: 引用数:
h-index:
机构:
Rathinasamy, Vignesh
[1
,2
]
论文数: 引用数:
h-index:
机构:
Tran, Lily
[1
,2
]
论文数: 引用数:
h-index:
机构:
Swan, Jaclyn
[1
,2
]
论文数: 引用数:
h-index:
机构:
Kelley, Jane
[1
,2
]
Hosking, Chris
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Hosking, Chris
[1
,2
]
Williamson, Genevieve
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Williamson, Genevieve
[1
,2
]
Knowles, Michaela
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Knowles, Michaela
[1
,2
]
Elliott, Timothy
论文数: 0引用数: 0
h-index: 0
机构:
Armidale Res Ctr, Invetus, Armidale, NSW, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Elliott, Timothy
[4
]
Rawlin, Grant
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, Australia
Dept Jobs Precincts & Reg, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Rawlin, Grant
[1
,2
,3
]
Spithill, Terry W.
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Spithill, Terry W.
[1
,2
]
Beddoe, Travis
论文数: 0引用数: 0
h-index: 0
机构:
La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, AustraliaLa Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
Beddoe, Travis
[1
,2
]
机构:
[1] La Trobe Univ, Dept Anim Plant & Soil Sci, Bundoora, Vic, Australia
[2] La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic, Australia
[3] Dept Jobs Precincts & Reg, Bundoora, Vic, Australia
[4] Armidale Res Ctr, Invetus, Armidale, NSW, Australia
Livestock production around the world is impacted by liver fluke (Fasciola spp.) infection resulting in serious economic losses to the beef, dairy and sheep industries with significant losses of about $90 million per annum in Australia. Triclabendazole (TCBZ) is the most effective anthelmintic treatment available to control liver fluke infections; however, the widespread emergence of TCBZ resistance in livestock threatens liver fluke control. Alternative control measures to lower exposure of livestock to liver fluke infection would help to preserve the usefulness of current anthelmintic treatments. Environmental DNA (eDNA) based identification of liver fluke and the intermediate snail host in the water bodies is a robust method to assess the risk of liver fluke infection on farms. In this study, we used a multiplex quantitative PCR assay of water samples to detect and quantify eDNA of Fasciola hepatica (F. hepatica) and Austropeplea tomentosa (A. tomentosa), a crucial intermediate snail host for liver fluke transmission in South-east Australia. Water samples were collected from an irrigation channel for a period of 7 months in 2016 (February, March, May, September, October, November and December) at a dairy farm located at Maffra, Victoria, South-east Australia. Using an effective eDNA extraction method, the multiplex qPCR assay allows for the independent but simultaneous detection of eDNA released from liver fluke life stages and snails using specific primers and a probe targeting the ITS-2 region of the liver fluke and snail, respectively, with minimal inhibition from contaminants in field collected water samples. The sensitivity of this assay to detect eDNA of liver fluke and snails was observed to be 14 fg and 50 fg, respectively, in the presence of field collected water samples. Differential levels of liver fluke and snail specific eDNA in water were observed at the time points analysed in this study. The successful detection of eDNA specific to liver fluke and snails from the field collected water samples provides a precedent for the use of this method as a monitoring tool to determine the prevalence of liver fluke and liver fluke-transmitting snails in irrigation regions. Further, this method has the enormous potential to allow an assessment of the liver fluke transmission zones on farms and to inform the application of effective control strategies.