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1.
Vector Borne Zoonotic Dis ; 9(6): 583-8, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19125658

ABSTRACT

Raccoons are the reservoir for the raccoon rabies virus variant in the United States. To combat this threat, oral rabies vaccination (ORV) programs are conducted in many eastern states. To aid in these efforts, the genetic structure of raccoons (Procyon lotor) was assessed in southwestern Pennsylvania to determine if select geographic features (i.e., ridges and valleys) serve as corridors or hindrances to raccoon gene flow (e.g., movement) and, therefore, rabies virus trafficking in this physiographic region. Raccoon DNA samples (n = 185) were collected from one ridge site and two adjacent valleys in southwestern Pennsylvania (Westmoreland, Cambria, Fayette, and Somerset counties). Raccoon genetic structure within and among these study sites was characterized at nine microsatellite loci. Results indicated that there was little population subdivision among any sites sampled. Furthermore, analyses using a model-based clustering approach indicated one essentially panmictic population was present among all the raccoons sampled over a reasonably broad geographic area (e.g., sites up to 36 km apart). However, a signature of isolation by distance was detected, suggesting that widths of ORV zones are critical for success. Combined, these data indicate that geographic features within this landscape influence raccoon gene flow only to a limited extent, suggesting that ridges of this physiographic system will not provide substantial long-term natural barriers to rabies virus trafficking. These results may be of value for future ORV efforts in Pennsylvania and other eastern states with similar landscapes.


Subject(s)
Genetics, Population , Geography , Raccoons/genetics , Administration, Oral , Animals , DNA Primers , Disease Reservoirs , Genotype , Markov Chains , Models, Genetic , Pennsylvania , Population Dynamics , Rabies Vaccines , Raccoons/virology
2.
Emerg Infect Dis ; 14(12): 1849-54, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19046506

ABSTRACT

To provide molecular and virologic evidence that domestic dog rabies is no longer enzootic to the United States and to identify putative relatives of dog-related rabies viruses (RVs) circulating in other carnivores, we studied RVs associated with recent and historic dog rabies enzootics worldwide. Molecular, phylogenetic, and epizootiologic evidence shows that domestic dog rabies is no longer enzootic to the United States. Nonetheless, our data suggest that independent rabies enzootics are now established in wild terrestrial carnivores (skunks in California and north-central United States, gray foxes in Texas and Arizona, and mongooses in Puerto Rico), as a consequence of different spillover events from long-term rabies enzootics associated with dogs. These preliminary results highlight the key role of dog RVs and human-dog demographics as operative factors for host shifts and disease reemergence into other important carnivore populations and highlight the need for the elimination of dog-related RVs worldwide.


Subject(s)
Animals, Wild/virology , Carnivora/virology , Communicable Diseases, Emerging/epidemiology , Dog Diseases/epidemiology , Rabies/veterinary , Zoonoses/epidemiology , Animals , Communicable Diseases, Emerging/virology , Dog Diseases/prevention & control , Dog Diseases/virology , Dogs , Foxes/virology , Herpestidae/virology , Humans , Mephitidae/virology , Nucleoproteins/genetics , Phylogeny , Rabies/epidemiology , Rabies/prevention & control , Rabies/virology , Rabies virus/genetics , Rabies virus/isolation & purification , Sequence Analysis, DNA , United States/epidemiology , Zoonoses/virology
3.
PLoS Pathog ; 4(11): e1000212, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19023410

ABSTRACT

Over the past 30 years, Zaire and Sudan ebolaviruses have been responsible for large hemorrhagic fever (HF) outbreaks with case fatalities ranging from 53% to 90%, while a third species, Côte d'Ivoire ebolavirus, caused a single non-fatal HF case. In November 2007, HF cases were reported in Bundibugyo District, Western Uganda. Laboratory investigation of the initial 29 suspect-case blood specimens by classic methods (antigen capture, IgM and IgG ELISA) and a recently developed random-primed pyrosequencing approach quickly identified this to be an Ebola HF outbreak associated with a newly discovered ebolavirus species (Bundibugyo ebolavirus) distantly related to the Côte d'Ivoire ebolavirus found in western Africa. Due to the sequence divergence of this new virus relative to all previously recognized ebolaviruses, these findings have important implications for design of future diagnostic assays to monitor Ebola HF disease in humans and animals, and ongoing efforts to develop effective antivirals and vaccines.


Subject(s)
Disease Outbreaks , Ebolavirus/isolation & purification , Hemorrhagic Fever, Ebola/virology , Antigens, Viral/analysis , Base Sequence , Enzyme-Linked Immunosorbent Assay , Hemorrhagic Fever, Ebola/epidemiology , Humans , RNA, Viral/genetics , Uganda/epidemiology
4.
J Virol ; 82(22): 11152-66, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18786992

ABSTRACT

Rift Valley fever (RVF) virus historically has caused widespread and extensive outbreaks of severe human and livestock disease throughout Africa, Madagascar, and the Arabian Peninsula. Following unusually heavy rainfall during the late autumn of 2006, reports of human and animal illness consistent with RVF virus infection emerged across semiarid regions of the Garissa District of northeastern Kenya and southern Somalia. Following initial RVF virus laboratory confirmation, a high-throughput RVF diagnostic facility was established at the Kenyan Central Veterinary Laboratories in Kabete, Kenya, to support the real-time identification of infected livestock and to facilitate outbreak response and control activities. A total of 3,250 specimens from a variety of animal species, including domesticated livestock (cattle, sheep, goats, and camels) and wildlife collected from a total of 55 of 71 Kenyan administrative districts, were tested by molecular and serologic assays. Evidence of RVF infection was found in 9.2% of animals tested and across 23 districts of Kenya, reflecting the large number of affected livestock and the geographic extent of the outbreak. The complete S, M, and/or L genome segment sequence was obtained from a total of 31 RVF virus specimens spanning the entire known outbreak period (December-May) and geographic areas affected by RVF virus activity. Extensive genomic analyses demonstrated the concurrent circulation of multiple virus lineages, gene segment reassortment, and the common ancestry of the 2006/2007 outbreak viruses with those from the 1997-1998 east African RVF outbreak. Evidence of recent increases in genomic diversity and effective population size 2 to 4 years prior to the 2006-2007 outbreak also was found, indicating ongoing RVF virus activity and evolution during the interepizootic/epidemic period. These findings have implications for further studies of basic RVF virus ecology and the design of future surveillance/diagnostic activities, and they highlight the critical need for safe and effective vaccines and antiviral compounds to combat this significant veterinary and public health threat.


Subject(s)
Disease Outbreaks , Rift Valley Fever/veterinary , Rift Valley fever virus/classification , Rift Valley fever virus/isolation & purification , Animals , Animals, Domestic , Camelus , Cattle , Cattle Diseases/virology , Cluster Analysis , Genotype , Goat Diseases/virology , Goats , Humans , Kenya/epidemiology , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , Rift Valley Fever/virology , Rift Valley fever virus/genetics , Sequence Analysis, DNA , Serotyping , Sheep , Sheep Diseases/virology
5.
J Gen Virol ; 87(Pt 8): 2309-2321, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16847127

ABSTRACT

Bats represent the major source of human rabies cases in the New World. In the USA, most cases are associated with species that are not commonly found or reported rabid. To understand better the epidemiology and public health significance of potentially important bat species, a molecular study was performed on samples collected from naturally infected rabid western pipistrelle (Pipistrellus hesperus), eastern pipistrelle (Pipistrellus subflavus) and silver-haired bats (Lasionycteris noctivagans) from different regions of their geographical distribution in the USA. A 264 bp fragment at the 5' end of the N gene coding region was sequenced and analysed in comparison with rabies virus variants circulating within other North American mammals. Phylogenetic analysis demonstrated that P. hesperus bats maintain a unique rabies virus variant. Preliminary data also suggest that P. subflavus and Lasionycteris noctivagans may harbour two different rabies virus variants (Ps and Ln) that are likely to be maintained independently by each bat species, which recently appear to have emerged as major vectors of human disease.


Subject(s)
Chiroptera/virology , Rabies virus/classification , Rabies virus/genetics , Rabies/veterinary , Rabies/virology , Amino Acid Sequence , Animals , Genome, Viral , Geography , Humans , Molecular Sequence Data , Nucleocapsid Proteins/genetics , Phylogeny , Rabies virus/isolation & purification , Sequence Analysis, DNA , United States
6.
Mol Phylogenet Evol ; 40(1): 251-8, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16626977

ABSTRACT

Recently, sequences from two nuclear genes (exon 6 of the dentin matrix protein 1 gene and intron 7 of the beta-fibrinogen gene) and one mitochondrial gene (cytochrome b gene) were used independently in an attempt to resolve phylogenetic relationships within the neotomine-peromyscine complex. Although these studies provided testable hypotheses regarding this group of rodents, the affinities of certain tribes and genera remain uncertain. To elucidate these relationships, the three data partitions were tested for heterogeneity and then concatenated according to conditional data combination and total evidence approaches. Support was found for five clades, four of which correspond to well recognized tribes (the Neotomini, Peromyscini=Reithrodontomyini, Baiomyini, and Tylomyini). Recommendations are made regarding the recognition of Ochrotomys as a tribe of its own, the Ochrotomyini, paralleling other recent findings. The Peromyscini, Baiomyini, and Ochrotomyini are unresolved in relation to each other, but as a whole are sister to the Neotomini. The Tylomyini is basal to all clades. It appears that combined data from the nuclear and mitochondrial genes (analyzing all three partitions simultaneously) resulted in the best phylogenetic hypothesis regarding the complex.


Subject(s)
Cell Nucleus/genetics , DNA, Mitochondrial/genetics , Rodentia/genetics , Animals , Base Sequence , Cytochromes b/genetics , Extracellular Matrix Proteins/genetics , Fibrinogen/genetics , Phosphoproteins/genetics , Phylogeny , Rodentia/classification
7.
J Wildl Dis ; 41(1): 1-11, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15827206

ABSTRACT

Sin Nombre virus (SNV) is an etiologic agent of hantavirus pulmonary syndrome. To better understand the natural history of this virus we studied population dynamics and temporal pattern of infection of its rodent hosts in southeastern Colorado (USA) from 1995 to 2000. We present evidence for the presence of two hantaviruses, SNV in deer mice (Peromyscus maniculatus) and El Moro Canyon virus in western harvest mice (Reithrodontomys megalotis), at our study sites. Sin Nombre virus appeared only sporadically in deer mouse populations; overall prevalence of antibody to SNV was 2.6%. El Moro Canyon virus was enzootic: seroconversions occurred throughout the year; antibody prevalence (11.9% overall) showed a delayed-density-dependent pattern, peaking as relative abundance of mice was declining. Males of both host species were more frequently infected than were females. An apparently lower mean survivorship (persistence at the trapping site) for SNV antibody-positive deer mice could indicate a detrimental effect of SNV on its host, but might also be explained by the fact that antibody-positive mice were older when first captured.


Subject(s)
Antibodies, Viral/blood , Arvicolinae/virology , Hantavirus Pulmonary Syndrome/veterinary , Peromyscus/virology , Rodent Diseases/epidemiology , Sin Nombre virus/immunology , Age Factors , Animals , Colorado/epidemiology , Female , Geography , Orthohantavirus/immunology , Hantavirus Infections/epidemiology , Hantavirus Infections/veterinary , Hantavirus Pulmonary Syndrome/epidemiology , Incidence , Longevity , Male , Rodent Diseases/virology , Rodentia , Seasons , Seroepidemiologic Studies , Sex Factors
8.
J Wildl Dis ; 41(1): 12-28, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15827207

ABSTRACT

We followed seasonal and year-to-year population dynamics for a diverse rodent assemblage in a short-grass prairie ecosystem in southeastern Colorado (USA) for 6 yr. We captured 2,798 individual rodents (range, one to 812 individuals per species) belonging to 19 species. The two most common species, deer mice (Peromyscus maniculatus) and western harvest mice (Reithrodontomys megalotis), generally had population peaks in winter and nadirs in summer; several other murid species demonstrated autumn peaks and spring nadirs; heteromyids were infrequently captured in winter, and populations generally peaked in summer or autumn. Inter-annual trends indicated an interactive effect between temperature and precipitation. Conditions associated with low rodent populations or population declines were high precipitation during cold periods (autumn and winter) and low precipitation during warm periods (spring and summer). Severity of adverse effects varied by species. Heteromyids, for example, were apparently not negatively affected by the hot, dry spring and summer of 2000. Cross-correlations for the temporal series of relative population abundances between species pairs (which are affected by both seasonal and interannual population dynamics) revealed positive associations among most murids and among most heteromyids, but there were negative associations between murids and heteromyids. These results have important implications for those attempting to model population dynamics of rodent populations for purposes of predicting disease risk.


Subject(s)
Rodentia/classification , Rodentia/growth & development , Animals , Climate , Colorado , Female , Geography , Male , Phylogeny , Population Density , Population Dynamics , Rodentia/physiology , Seasons
9.
Mol Phylogenet Evol ; 26(1): 89-101, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12470941

ABSTRACT

We sequenced exon 6 of the nuclear dentin matrix protein 1 (DMP1) gene from 19 species of bats (order Chiroptera) to assess the utility of this gene for higher-level phylogenetic studies. Bayesian analysis revealed high support (posterior probabilities >/=0.95) for monophyly of Noctilionoidea (Phyllostomidae, Noctilionidae, and Mormoopidae), all genera and most families examined. Comparison of the phylogenetic information present in DMP1 with mitochondrial rDNA and nuclear RAG2 genes indicated no significant heterogeneity. Thus, we concatenated these three data sets into a single "total evidence" phylogenetic analysis. Combined analysis was congruent with study of RAG2 and combined RAG2 and mtrDNA sequences, but improved support (Bayesian posterior probabilities) for many nodes. Our results indicate that exon 6 of DMP1 is rapidly evolving, able to tolerate non-frame shifting insertion and deletion events, is more variable than RAG2, and provides phylogenetic resolution from the interfamilial to infraclass levels in mammals.


Subject(s)
Chiroptera/genetics , Evolution, Molecular , Phosphoproteins/genetics , Phylogeny , Amino Acid Sequence , Animals , Molecular Sequence Data , Sequence Alignment
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