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1.
Environ Entomol ; 53(1): 11-17, 2024 Feb 20.
Article in English | MEDLINE | ID: mdl-37478402

ABSTRACT

The beet leafhopper, Circulifer tenellus (Baker 1896), is the sole vector of beet curly top virus (BCTV). Both the virus and the vector have very wide host ranges, including many crops and weeds. Industrial hemp (Cannabis sativa L.) has been reported as a host for both the virus and leafhopper in the past few years with the legal cultivation of the crop in the United States. This research assessed the interactions of the beet leafhopper and hemp in New Mexico by determining the natural infection of hemp with BCTV in 3 field plots in 2021 and 2022 and monitoring the numbers of leafhoppers using yellow sticky traps. The relative preference of beet leafhopper for hemp types and varieties of hemp was assessed using cafeteria-style choice tests. Higher numbers of beet leafhoppers were trapped in and around hemp fields in 2022 than in 2021 in all 3 locations. BCTV was found to infect all 3 types of hemp (cannabidiol or CBD, fiber, and grain) in 2022 in 1 location and only a single CBD variety of hemp in the other 2 locations. Two BCTV strains were identified in CBD hemp, while an additional BCTV strain was found infecting chile pepper grown at the same location.


Subject(s)
Beta vulgaris , Cannabis , Geminiviridae , Hemiptera , Animals , New Mexico , Plant Diseases
2.
J Med Entomol ; 46(6): 1474-82, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19960700

ABSTRACT

The potential vectors of West Nile virus (family Flaviviridae, genus Flavivirus, WNV) in Doña Ana County, NM, were determined during 2004 and 2005. Trapping was conducted using Centers for Disease Control and Prevention miniature light-traps baited with dry ice, and gravid traps baited with a hay infusion. In addition, sentinel chickens were housed at four of the trapping locations to monitor WNV epizootic transmission. In total, 5,576 pools consisting of 115,797 female mosquitoes were tested for WNV by reverse transcription-polymerase chain reaction, of which 152 from 13 mosquito species representing six genera were positive. Culex tarsalis Coquillett, Culex quinquefasciatus Say, Culex erythrothorax Dyar, Aedes vexans (Meigan), and Psorophora columbiae (Dyar & Knab) accounted for 86% of all detections. Based on the frequency of WNV detection, our data indicate primary and secondary vector roles for Cx. tarsalis and Cx. quinquefasciatus, respectively, with Cx. erythrothorax, Ae. vexans, and Ps. columbiae as occasional vectors of WNV in Dofia Ana County. Other species testing positive for the virus included Aedes aegypti (L.), Anopheles franciscanus McCracken, Culex stigmatosoma Dyar, Culiseta inornata (Williston), Ochlerotatus dorsalis (Meigan), Ochlerotatus sollicitans (Walker), Ochlerotatus trivittatus (Coquillett), and Psorophora signipennis (Coquillett). Although they occurred after initial WNV detections in mosquitoes, in total, 21 seroconversions in sentinel chickens were detected during the study.


Subject(s)
Climate , Culicidae/virology , Insect Vectors/virology , West Nile virus , Animals , Culicidae/classification , DNA, Viral/isolation & purification , Female , New Mexico , Reverse Transcriptase Polymerase Chain Reaction , Seasons
3.
Arch Virol ; 154(3): 429-36, 2009.
Article in English | MEDLINE | ID: mdl-19198754

ABSTRACT

Over 4,950 asymptomatic weed samples from more than 20 weed species that are host plants for curtoviruses were collected from ten chile pepper fields in southern New Mexico (NM) during 2003, 2004 and 2005 to identify whether they were infected with curtoviruses and to determine which curtoviruses were distributed in the weed population. Polymerase chain reaction using primers designed to detect a portion of the coat protein (cp) gene were used to detect curtoviruses, and infected plants were further tested for specific curtoviruses using primers designed to detect to a portion of the replication-associated protein (rep) gene. Amplification of the cp gene was successful from 3.7, 1.17, and 1.9% of the weed samples in 2003, 2004, and 2005, respectively. Seventy-three amplicons from those samples were sequenced and compared to well-characterized curtoviruses. Analysis of the rep nucleotide sequences showed that approximately 32.9% of the weed isolates tested were closely related to beet mild curly top virus (BMCTV). Approximately 12.4% were closely related to beet severe curly top virus (BSCTV). The rest of the weed isolates (54.7%), which shared a very high level of nucleotide sequence identity to each other, represent a new curtovirus species. Using eight primers designed for PCR, complete genomes of three curtoviruses isolated from chile pepper samples representing the three groups of curtoviruses in southern New Mexico were sequenced. Comparisons of whole sequences of the genomes revealed that the DG2SW171601 isolate (2,929 nucleotides) was nearly identical to BMCTV-W4 (approximately 98% nucleotide sequence identity). The LRME27601 isolate (2,927 nucleotides) was most closely related to BSCTV (approximately 92% nucleotide sequence identity). The LJN17601 isolate (2,959 nucleotides) shared only from 49.9 to 88.8% nucleotide sequence identity with other well-characterized curtoviruses. Based on the accepted cut-off of 89%, we propose that the LJN17601 isolate is a member of a new curtovirus species. Chile peppers infected with this virus in the field express chlorotic stunting symptoms, so we propose the name pepper yellow dwarf virus (PeYDV). This new curtovirus species may be the result of mutations in the genome and recombination between BMCTV-W4 and BSCTV.


Subject(s)
Geminiviridae/isolation & purification , Magnoliopsida/virology , Cluster Analysis , DNA, Viral/chemistry , DNA, Viral/genetics , Molecular Sequence Data , New Mexico , Phylogeny , Polymerase Chain Reaction/methods , Sequence Analysis, DNA , Sequence Homology
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