2013
DOI: 10.1645/12-4.1
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Severe Ulceronecrotic Dermatitis Associated with Mite Infestation in the Critically Endangered Amargosa Vole (Microtus californicus scirpensis)

Abstract: The entire range of the critically endangered Amargosa vole (Microtus californicus scirpensis) consists of less than 20 km(2) of riparian habitat in the Amargosa River drainage of the Mojave Desert in southern California. In September 2010, deformities on ears and chiggers on the ears and genitalia were detected, with some individuals so severely affected that they were missing ear pinnae altogether. Follow-up trapping was performed to document the presence of mites and mite-associated disease, and molecular c… Show more

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Cited by 16 publications
(8 citation statements)
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“…Mites were pierced with a sterile needle to facilitate DNA extraction, followed by DNA isolation using the QIAmp DNA Micro Kit (Qiagen, Hilden, Germany) according to manufacturer instructions. PCR primers were used in a 25-μL volume PCR reaction containing GoTaq Green Master Mix (Promega, Madison, WI), with cycling conditions as previously described ( Black and Piesman, 1994 ; Morelli and Spicer, 2007 ; Dowling and Oconnor, 2010 ; Foley et al., 2013 ). PCR products were visualized on a 1% agarose gel and purified using ExoSAP-IT (ThermoFisher, West Sacramento, CA) before sequencing on an ABI 3730 sequencer (UCDNA Sequencing Facility, Davis, CA) using the forward primer.…”
Section: Methodsmentioning
confidence: 99%
“…Mites were pierced with a sterile needle to facilitate DNA extraction, followed by DNA isolation using the QIAmp DNA Micro Kit (Qiagen, Hilden, Germany) according to manufacturer instructions. PCR primers were used in a 25-μL volume PCR reaction containing GoTaq Green Master Mix (Promega, Madison, WI), with cycling conditions as previously described ( Black and Piesman, 1994 ; Morelli and Spicer, 2007 ; Dowling and Oconnor, 2010 ; Foley et al., 2013 ). PCR products were visualized on a 1% agarose gel and purified using ExoSAP-IT (ThermoFisher, West Sacramento, CA) before sequencing on an ABI 3730 sequencer (UCDNA Sequencing Facility, Davis, CA) using the forward primer.…”
Section: Methodsmentioning
confidence: 99%
“…We heated samples at 100 C for 15 min with 100 mL of 0.7 M NH 4 OH and then cooled samples on ice for 30 sec, followed by 15 min of heating at 100 C with open lids to evaporate ammonia. We viewed mites with a compound microscope to confirm them as being larval Neotrombicula microti (Foley et al 2013) and then extracted mites individually as for ticks. We viewed lice with a dissecting microscope and identified them as either biting or sucking lice but did not further test, as this was outside the scope of our survey for pathogens.…”
Section: Field Studiesmentioning
confidence: 99%
“…For instance, Amargosa voles experience severe and highly prevalent lesions due to chiggers [ 115 ], while California voles (the larger species of which Amargosa voles are a subspecies) have been shown to be fatally susceptible to plague and tularemia [ 6 , 116 ]. Chiggers on Amargosa voles are highly prevalent, and often associated with severe lesions, although their presence did not appear to impact body mass or fitness [ 117 ]. The fleas O .…”
Section: Discussionmentioning
confidence: 99%