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1.
Insect Mol Biol ; 27(2): 177-187, 2018 04.
Article in English | MEDLINE | ID: mdl-29164729

ABSTRACT

Lipocalins are low molecular weight membrane transporters that are abundantly expressed in the salivary glands and other tissues of ticks. In this study, we identified a lipocalin-like molecule, designated as otlip, from the soft ticks Ornithodoros turicata, the vector for the relapsing fever causing spirochete Borrelia turicatae. We noted that the expression of otlip was developmentally regulated, with adult ticks expressing significantly higher levels in comparison to the larvae or nymphal ticks. Expression of otlip was evident in both fed and unfed O. turicata ticks, with significantly increased expression in the salivary glands in comparison to the midgut or ovary tissues. High conservation of the biogenic amine-binding motif was evident in the deduced primary amino acid sequence of Otlip. Protein modelling of Otlip revealed conservation of most of the residues involved in binding histamine or serotonin ligand. In vitro assays demonstrated binding of recombinant Otlip with histamine. Furthermore, prediction of post-translational modifications revealed that Otlip contained phosphorylation and myristoylation sites. Taken together, our study not only provides evidence for the presence of a lipocalin-like molecule in O. turicata ticks but also suggests a role for this molecule in the salivary glands of this medically important vector.


Subject(s)
Arthropod Proteins/genetics , Gene Expression , Histamine/metabolism , Lipocalins/genetics , Ornithodoros/genetics , Amino Acid Sequence , Animals , Arthropod Proteins/chemistry , Arthropod Proteins/metabolism , Base Sequence , Female , Gene Expression Profiling , Larva/genetics , Larva/growth & development , Larva/metabolism , Lipocalins/chemistry , Lipocalins/metabolism , Nymph/genetics , Nymph/growth & development , Nymph/metabolism , Ornithodoros/growth & development , Ornithodoros/metabolism , Phylogeny , Salivary Glands/metabolism , Sequence Alignment
2.
Insect Mol Biol ; 25(1): 72-92, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26783017

ABSTRACT

Illumina GAII high-throughput sequencing was used to compare expressed genes for female synganglion neuropeptides, neuropeptide receptors and neurotransmitter receptors of the soft tick Ornithodoros turicata with the hard tick Ixodes scapularis. Gene ontology molecular level three mapping revealed no significant differences amongst the same categories represented in O. turicata and I. scapularis. Transcripts predicting 22 neuropeptides or their receptors in the O. turicata synganglion were similar to annotations for 23 neuropeptides or receptors previously identified from I scapularis, with minor exceptions. A transcript predicting ecdysis triggering hormone receptor was identified in O. turicata; transcripts encoding for proprotein convertase and glycoprotein B were identified in both species. Transcripts predicting the same neurotransmitter receptors were found in the synganglion of both species. Gene expression of the transcripts showed numerous differences in response to feeding. Major differences were observed in expression of genes believed important in regulating slow vs. rapid feeding, blood water elimination, cuticle synthesis plasticity and in signalling reproductive activity. Although the glutamate receptor was strongly upregulated in both species, the gamma aminobutyric acid receptor, which inhibits glutamate, was upregulated significantly only in I. scapularis. These differences are consistent with the slow vs. rapid action of the pharyngeal pump in the two species.


Subject(s)
Insect Proteins/metabolism , Ixodes/metabolism , Neuropeptides/metabolism , Ornithodoros/metabolism , Receptors, Neuropeptide/metabolism , Animals , Diuresis , Feeding Behavior , Female , Ganglion Cysts/metabolism , Gene Expression , Gene Ontology , Molting , Reproduction , Salivary Glands/metabolism
3.
Med Vet Entomol ; 27(1): 86-95, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22681499

ABSTRACT

Carbon dioxide (CO(2) ), 1-octen-3-ol, acetone, ammonium hydroxide, L-lactic-acid, dimethyl trisulphide and isobutyric acid were tested as attractants for two tick species, Amblyomma americanum and Dermacentor variabilis (Acari: Ixodidae), in dose-response bioassays using Y-tube olfactometers. Only CO(2) , acetone, 1-octen-3-ol and ammonium hydroxide elicited significant preferences from adult A. americanum, and only CO(2) was attractive to adult D. variabilis. Acetone, 1-octen-3-ol and ammonium hydroxide were separately evaluated at three doses against CO(2) (from dry ice) at a field site supporting a natural population of A. americanum nymphs and adults. Carbon dioxide consistently attracted the highest number of host-seeking ticks. However, for the first time, acetone, 1-octen-3-ol and ammonium hydroxide were shown to attract high numbers of A. americanum. Further research is needed to determine the utility of these semiochemicals as attractants in tick surveillance and area-wide management programmes.


Subject(s)
Ixodidae/drug effects , Ixodidae/physiology , Pheromones/pharmacology , Animals , Dermacentor/drug effects , Dermacentor/physiology , Feeding Behavior/drug effects , Insect Control , Species Specificity
4.
Insect Mol Biol ; 21(2): 197-204, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22221256

ABSTRACT

Alpha catenin is a cytoskeleton protein that acts as a regulator of actin rearrangement by forming an E-cadherin adhesion complex. In Dermacentor variabilis, a putative α-catenin (Dvα-catenin) was previously identified as differentially regulated in ovaries of ticks chronically infected with Rickettsia montanensis. To begin characterizing the role(s) of Dvα-catenin during rickettsial infection, the full-length Dvα-catenin cDNA was cloned and analysed. Comparative sequence analysis demonstrates a 3069-bp cDNA with a 2718-bp open reading frame with a sequence similar to Ixodes scapularisα-catenin. A portion of Dvα-catenin is homologous to the vinculin-conserved domain containing a putative actin-binding region and ß-catenin-binding and -dimerization regions. Quantitative reverse-transcription PCR analysis demonstrated that Dvα-catenin is predominantly expressed in tick ovaries and is responsive to tick feeding. The tissue-specific gene expression analysis of ticks exposed to Rickettsia demonstrates that Dvα-catenin expression was significantly downregulated 12 h after exposure to R. montanensis, but not in Rickettsia amblyommii-exposed ovaries, compared with Rickettsia-unexposed ticks. Studying tick-derived molecules associated with rickettsial infection will provide a better understanding of the transmission dynamics of tick-borne rickettsial diseases.


Subject(s)
Arthropod Proteins/metabolism , Arthropod Vectors/metabolism , Dermacentor/metabolism , Rickettsia/physiology , alpha Catenin/metabolism , Amino Acid Sequence , Animals , Arthropod Proteins/genetics , Arthropod Vectors/genetics , Dermacentor/genetics , Dermacentor/microbiology , Feeding Behavior , Female , Gene Expression , Molecular Sequence Data , RNA, Messenger/metabolism , Rickettsia Infections/transmission , Sequence Analysis, DNA , alpha Catenin/genetics
5.
Insect Mol Biol ; 20(4): 465-91, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21689185

ABSTRACT

454 Pyrosequencing was used to characterize the expressed genes from the synganglion and associated neurosecretory organs of unfed and partially fed virgin and mated replete females of the American dog tick, Dermacentor variabilis. A total of 14,881 contiguous sequences (contigs) was assembled, with an average size of 229 bp. Gene ontology terms for Level 2 biological processes were assigned to 4366 contigs. Seven acetylcholinesterases, a muscarinic acetylcholine (ACh) receptor, two nicotinic ACh receptor ß-subunits, two ACh unc-18 regulators, two dopamine receptors, two gamma aminobutyric acid (GABA) receptors, two GABA transporters, two norepinephrine transporters and an octopamine receptor are described. Microarrays were conducted to examine global gene expression and quantitative real-time polymerase chain reaction was used to verify expression of selected neuropeptides. Hierarchical clustering of all differentially expressed transcripts grouped part-fed and replete ticks as being more similar in terms of differentially expressed genes with unfed ticks as the outgroup. Nine putative neuropeptides (allatostatin, bursicon-ß, preprocorazonin, glycoprotein hormone α, insulin-like peptide, three orcokinins, preprosulphakinin) and a gonadotropin releasing hormone receptor were differentially expressed, and their developmental expression and role in reproduction was investigated. The presence of eclosion hormone, corazonin and bursicon in the synganglion, which in insects regulate behaviour and cuticle development associated with moulting, suggest that this system may be used in ticks to regulate blood feeding, cuticle expansion and development related to female reproduction; adult ticks do not moult.


Subject(s)
Dermacentor/metabolism , Hormones/metabolism , Neuropeptides/metabolism , Neurotransmitter Agents/metabolism , Acetylcholine/metabolism , Acetylcholinesterase/chemistry , Acetylcholinesterase/metabolism , Amino Acid Sequence , Animals , Central Nervous System/growth & development , Central Nervous System/metabolism , Dermacentor/genetics , Dermacentor/growth & development , Feeding Behavior , Female , Gene Expression Profiling , Molecular Sequence Data , Neurotransmitter Transport Proteins/genetics , Neurotransmitter Transport Proteins/metabolism , Oligonucleotide Array Sequence Analysis , Polymerase Chain Reaction , Receptors, GABA/chemistry , Receptors, GABA/metabolism , Receptors, Neurotransmitter/genetics , Receptors, Neurotransmitter/metabolism , Receptors, Nicotinic/chemistry , Receptors, Nicotinic/metabolism , Receptors, Steroid/metabolism , Sexual Behavior, Animal
6.
Med Vet Entomol ; 25(2): 202-8, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21073492

ABSTRACT

2-Tridecanone and 2-undecanone are both found naturally in the trichomes of wild tomato plants and are important in plant resistance to herbivory. 2-Undecanone is the U.S. Environmental Protection Agency (EPA)-registered active ingredient in the commercially available arthropod repellent, BioUD(®) . The goal of this study was to examine the tick repellency of 2-tridecanone. Two-choice bioassays were conducted using 8% 2-tridecanone vs. the repellent carrier (absolute ethanol) and compared with two-choice studies using 8% 2-undecanone vs. absolute ethanol. Unfed, host-seeking adult (mixed sex) Amblyomma americanum (L.) (Acari: Ixodidae) and Dermacentor variabilis Say (Acari: Ixodidae) were used to evaluate repellency and time to repellent failure at room temperature. The present study shows in filter paper assays (0.63 mg test compound/cm(2) ) that 2-tridecanone was 87% repellent to A. americanum at 12 h after application, but had no statistically significant repellency at 15 h and 24 h, and was 72% repellent to D. variabilis at 15 h, but had no statistically significant repellency at 24 h. By contrast, 2-undecanone was 74% and 75% repellent to A. americanum and D. variabilis, respectively, at 2 h after application, but no statistically significant repellency was noted at 2.5 h and 3 h. In two-choice assays on cheesecloth, 2-tridecanone at 0.25 mg/cm(2) was 85% repellent to A. americanum 6 h after application, demonstrating its potential use as an arthropod repellent that can be used on clothing without the need for formulation. No statistically significant repellency was found at 9 h or 12 h. The potential use of 2-tridecanone as a tick repellent is discussed.


Subject(s)
Dermacentor/drug effects , Insect Control/methods , Insect Repellents/pharmacology , Ixodidae/drug effects , Ketones/pharmacology , Animals , Dermacentor/physiology , Ixodidae/physiology , North Carolina
7.
Med Vet Entomol ; 25(2): 217-26, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21118283

ABSTRACT

Two new field bioassay methods were developed to compare the repellent activity of BioUD(®) (containing 7.75% 2-undecanone), 98.1% DEET and 0.5% permethrin against natural populations of nymphal Amblyomma americanum (L.) (Acari: Ixodidae). In a cloth sheet assay, pieces of material measuring 41 × 58 cm, separately treated with one of the test materials or the appropriate solvent carrier, were placed at random on the ground and baited with dry ice for 1 h. Mean numbers of ticks on repellent-treated sheets were significantly lower than on control sheets. There was no significant difference in the number of ticks collected between sheets treated with BioUD(®) and those treated with DEET. However, significantly fewer ticks were found on sheets treated with BioUD(®) or DEET than on permethrin-treated sheets. In a sock test, over-the-calf tube socks were treated with one of the test materials or the appropriate solvent carrier. Human volunteers wore a repellent-treated and a corresponding carrier-treated sock on either leg and walked randomly over an area of approximately 4000 m(2) for 15 min. Significantly fewer ticks were collected from socks treated with BioUD(®) or DEET than from socks treated with the carrier and there was no significant difference in repellency between these two agents. No difference in the mean number of ticks collected was found between permethrin-treated and corresponding carrier-treated socks. To examine the mechanism of repellency of BioUD(®) , a four-choice olfactometer was used to assess spatial repellency against adult A. americanum. As expected in the absence of a repellent, when all choices were represented by water-treated filter paper, ticks were equally distributed among the choices. When one choice consisted of BioUD(®) -treated filter paper and the remaining choices of water-treated paper, the distribution of ticks on the repellent-treated paper was significantly lower than might be expected to occur by chance, suggesting that repellency is at least partly achieved by an olfactory mechanism.


Subject(s)
DEET , Insect Repellents , Ketones , Permethrin , Pest Control/methods , Animals , Female , Humans , Ixodidae/drug effects , Male , Nymph , Pest Control/instrumentation
8.
J Med Entomol ; 46(5): 1062-73, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19769037

ABSTRACT

The "kissing bugs," Triatoma dimidiata (Latreille) and Rhodnius prolixus (Stål) (Reduviidae: Triatominae) are major vectors of Chagas disease in Central and South America. To further uncover the attraction to certain host cues by these vectors at long and short distances from their host, the behavioral responses of two life stages (fifth-instar nymphs and adult males) of these two species to different known or suspected attractants, alone or in combination, were investigated. Tests were done using short- and long-range environments, namely, a four-port olfactometer and a long-range artificial chamber designed to mimic the insect's natural habitats. In single-attractant trials, heat alone and CO2 alone were found to be more attractive than selected chemicals. In multiple-attractant trials, both species and life stages were attracted at short distances, and a statistically significant synergistic increase in attraction was observed in long-distance multimodal tests. Lures containing CO2 were the most effective attractants at both long and short distances. R. prolixus adult males were significantly less attracted to several lure combinations than the nymphs of either species, perhaps because adults were more motivated to seek mates than feed. Our findings suggest that although the triatomine bugs may be capable of detecting odorants and heat sources at short distances, their ability to locate a host over a long distance is best aided by the presence of a CO2 plume.


Subject(s)
Carbon Dioxide/chemistry , Insect Control/methods , Odorants , Rhodnius , Triatoma , Animals , Hot Temperature , Male , Pheromones/chemistry
9.
Exp Appl Acarol ; 48(3): 239-50, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19140016

ABSTRACT

BioUD with the active ingredient 2-undecanone originally derived from wild tomato plants is a new repellent recently registered by the US EPA. Repellent efficacy of BioUD (7.75% 2-undecanone) and DEET (98.11%) was examined in the laboratory using a choice test between repellent-treated and control filter paper surfaces for Amblyomma americanum, Dermacentor variabilis, and Ixodes scapularis. BioUD provided greater repellency against A. americanum and I. scapularis than DEET. No difference was found between BioUD and DEET against D. variabilis. In head-to-head assays between BioUD and DEET, undiluted and 50% dilutions of BioUD were more repellent than undiluted DEET against all three species tested. Similarly, a 25% dilution of BioUD was more repellent than DEET against A. americanum while no difference in mean percentage repellency was found between a 25% dilution of BioUD and DEET against I. scapularis. Based on regression analysis, the concentration of BioUD required for equivalent repellency to 98.11% DEET was 39.5% for D. variabilis and 29.7% for I. scapularis. A log-probit model could not be constructed for A. americanum from the dosages tested. Based on filter paper head-to-head assays, BioUD is at least 2-4 times more active as a repellent than DEET against three species of ixodid ticks under the conditions of our laboratory bioassays.


Subject(s)
Insect Repellents , Ixodidae/drug effects , Ketones , Animals , DEET , Species Specificity
10.
Insect Mol Biol ; 17(3): 197-208, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18477238

ABSTRACT

The major hemelipoglyco-carrier protein (CP) found throughout the development of male and female adult American dog ticks, Dermacentor variabilis (Say) was sequenced. DvCP is a single transcript coding for two protein subunits that together contain three motifs: (1) a lipoprotein n-terminal domain that is a common attribute of proteins that bind lipids, carbohydrates and metals; (2) a domain of unknown function characteristic of proteins with several large open beta sheets; and (3) a von Willebrand factor type D domain near the carboxy-terminus apparently important for multimerization. These motifs, which are also found in tick vitellogenin, are not shared by heme-binding proteins studied thus far in other hematophagous insects. DvCP message was highest in fat body and salivary gland but was also found in midgut and ovary tissue. Expression was initiated by blood feeding in virgin females and not by mating, as is typical of tick vitellogenin; and the message was found in fed males at levels similar to part fed, virgin females. CP appears to be highly conserved among the Ixodida. The closest match by BlastP to DvCP is vitellogenin from Caenorhabditis elegans (AAC04423), suggesting that CP is a novel protein. The role of CP in heme sequestration, the evolution of hematophagy and host complementation are discussed.


Subject(s)
Dermacentor/genetics , Glycoproteins/genetics , Amino Acid Sequence , Animals , Feeding Behavior , Female , Gene Expression Regulation, Developmental , Glycoproteins/chemistry , Hemolymph/chemistry , Molecular Sequence Data , Organ Specificity , Peptides/chemistry , Phylogeny , Rabbits , Rats , Saliva/chemistry , Sequence Alignment , Sequence Analysis, DNA , Sequence Homology, Amino Acid
11.
Insect Mol Biol ; 17(1): 87-9, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18237287

ABSTRACT

VectorBase, an integrated, relational database that manages genomic and other genetic/biological data pertaining to arthropod vectors of disease, has recently embarked on the construction of ontologies and controlled vocabularies (CVs). It aims, thus, at providing all necessary tools for the complete annotation of vector genomes and, in particular, the annotation of functional genomic data. This task was initiated with the development of anatomical ontologies of mosquitoes and ticks, both of which were made compliant to CARO, the common anatomy reference ontology. The ontologies are complemented by the development of novel web-based browsers that can show figures for anatomical terms, something that is especially helpful for fully illustrating the controlled vocabularies of anatomy.


Subject(s)
Culicidae/anatomy & histology , Insect Vectors/anatomy & histology , Ticks/anatomy & histology , Animals , Culicidae/genetics , Databases, Factual , Databases, Genetic , Insect Vectors/genetics , Internet , Ticks/genetics
12.
Med Vet Entomol ; 21(2): 141-7, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17550433

ABSTRACT

The transcript sequence of the Amblyomma americanum Linnaeus (Acari: Ixodidae) defensin, termed amercin (amn), was ascertained and a 219-bp amn coding region identified. The gene encodes a 72-amino acid prepropeptide with a putative 37-amino acid mature peptide. This gene shows little similarity to either of the defensins from Amblyomma hebraeum Koch, the only other Amblyomma species for which a defensin has been described. Sequence comparisons with other tick defensins reveal amn to be shorter (6 bp or 2 amino acids) than the Ixodes scapularis Linnaeus (Acari: Ixodidae) and Dermacentor variabilis (Say) (Acari: Ixodidae) defensin sequences. The amercin prepropeptide has 60.8% and 59.5% similarity with the I. scapularis and D. variabilis prepropeptides, respectively, whereas the mature amercin peptide has 73.7% and 71.1% similarity with the mature peptides of these ticks. Similarity with other tick defensins ranges from 42% to 71%. In A. americanum, defensin transcript was found in the midgut, fat body and salivary gland tissues, as well as in the haemocytes. Defensin transcript was also present in early-stage eggs (less than 48 h old), late-stage eggs (approximately 2 weeks old), larvae and nymphs of A. americanum and I. scapularis, both of which are vector-competent for Borrelia spirochetes.


Subject(s)
Arachnid Vectors/genetics , Defensins/genetics , Gene Expression/physiology , Ixodidae/physiology , Life Cycle Stages/genetics , Animals , Arachnid Vectors/growth & development , Arachnid Vectors/physiology , Base Sequence , DNA Primers/chemistry , DNA, Complementary/genetics , Defensins/analysis , Defensins/biosynthesis , Gene Expression Profiling/veterinary , Ixodidae/genetics , Ixodidae/growth & development , Life Cycle Stages/physiology , Molecular Sequence Data , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid
13.
Med Vet Entomol ; 19(4): 339-44, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16336297

ABSTRACT

The black-legged tick Ixodes scapularis Linnaeus (Acari: Ixodidae) is an important vector of microbial pathogens. Knowledge of the tick's innate immune response, particularly defensin and other antimicrobial peptides, is important for understanding how microbes survive in this tick. A defensin gene (slnA) from I. scapularis was obtained by reverse transcription-polymerase chain reaction (RT-PCR) using mRNA extracted from tissues of female ticks. RT-PCR indicated the gene was expressed in the midgut, haemocytes, and fat-body, although no evidence of a peptide was found. Sequencing a cloned cDNA fragment revealed a 225 bp open reading frame encoding a 74 amino acid pre-prodefensin, including the putative 38 amino acid mature peptide. Similarity between the defensin amino acid sequences of I. scapularis and Dermacentor variabilis (Say) (Acari: Ixodidae) was 62.2% for the pre-prodefensin region; for the mature defensins from these two species the similarity was 78.9%, with the six cysteine residues being located in the same relative position. PCR amplification and sequencing of chromosomal DNA suggests that slnA, along with vsnA, the defensin gene from D. variabilis, does not contain any introns. This is in contrast to the defensins described for the soft tick, Ornithodoros moubata (sensu Walton) (Acari: Argasidae). The role of defensin in the innate immune response of I. scapularis following microbial invasions is discussed.


Subject(s)
Defensins/metabolism , Insect Vectors/metabolism , Ixodes/metabolism , Amino Acid Sequence , Animals , Base Sequence , DNA Primers , DNA, Complementary/genetics , Defensins/genetics , Insect Vectors/genetics , Ixodes/genetics , Molecular Sequence Data , New York , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA , Sequence Homology , Species Specificity
14.
Parasitology ; 129 Suppl: S405-25, 2004.
Article in English | MEDLINE | ID: mdl-15938521

ABSTRACT

This review addresses the role of compounds secreted into the external environment that mediate important aspects of tick behaviour. Known as semiochemicals, these information-containing compounds include pheromones (used for conspecific communication), allomones (defence secretions) and kairomones (used for host identification and location). An impressive body of knowledge has accumulated concerning the identification of the compounds that comprise these semiochemicals. Pheromones are the best known and intensively studied, including arrestment (=assembly) pheromones, attraction-aggregation-attachment (AAA) pheromones and sex pheromones. Arrestment behaviour is mediated by contact with excreta from other ticks. In contrast, aggregating and sexual behaviours comprise a hierarchy of responses to different types of chemical compounds that must be recognized in a sequential order to achieve the end result. Ixodid ticks also produce an allomone that protects against certain insect predators. Finally, ticks use kairomones for host identification, e.g. volatiles such as CO2 and NH3 and various oils such as glandular secretions from deer. Knowledge of tick pheromones has been used to develop innovative new technologies for tick control. These products incorporate tick pheromones and small amounts of pesticide to attract and kill ticks on their hosts or in vegetation. The kairomones and the tick allomone also may be of interest for use in controlling ticks.


Subject(s)
Pheromones/physiology , Tick Control/methods , Ticks/physiology , Animals
15.
J Chem Ecol ; 28(1): 15-27, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11868671

ABSTRACT

The responses of Irodes scapularis (Acari: Ixodidae) nymphs and adults to extracts of cast larval skins were tested in a Petri dish bioassay. Assembly was elicited in nymphs and adults in the presence of skins, exudate from ticks, and filter paper exposed to ticks compared to untreated controls. Assembly was noted by 1 hr after exposure with little change between 1 and 24 hr. The assembly response increased in the presence of an increased number of skins. Similar assembly was elicited in nymphs and adults in the presence of cast larval skins and a saline (0.95% NaCl) skin extract. Methanol and hexane extracts were not attractive. When chemical standards were tested against nymphs, they responded to guanine, uric acid, hypoxanthine, xanthine, inosine, and hematin. Adults were tested against guanine, inosine, and xanthine, and all elicited significant assembly. Responses of nymphs increased significantly with increase in dose of uric acid and guanine. Responses of nymphs to a mixture of guanine, xanthine, and adenine (25:1:1 ratio) were similar to responses to cast skins. This study provides the first evidence of an assembly pheromone in I. scapularis.


Subject(s)
Ixodes/physiology , Pheromones/physiology , Animals , Behavior, Animal/physiology , Female , Male
16.
J Insect Physiol ; 48(3): 269-278, 2002 Mar.
Article in English | MEDLINE | ID: mdl-12770100

ABSTRACT

In comparison to insects and Crustacea, our knowledge of the predominant hemolymph proteins in ticks is minimal. The hemolymph protein most studied in ticks has been vitellogenin (Vg). Vg is synthesized by the tick fat body after female adults obtain a blood meal, is released into the hemolymph and is absorbed by developing oocytes as vitellin (Vn). Much of what we know about Vg is from studies of Vn. In general, the carbohydrate, lipid and amino acid composition is similar to insects except that in the tick, Vg contains heme, most likely from the digestion of host hemoglobin. In the American dog tick, Dermacentor variabilis, Vg is comprised of two native proteins and seven subunits on SDS-PAGE. Vg has been characterized in five tick species but the amino acid sequence is not yet available. Another predominant hemolymph protein, apparently a carrier protein (CP), has recently been studied in two tick species. This protein is found in the hemolymph of both male and females adults, in adult tissues outside of the hemolymph in some tick species, in coxal fluid of soft ticks and in whole body homogenates from eggs, larvae and nymphs. CP from the hard tick, D. variabilis, contains cholesterol, phospholipids, monoacylglycerides, triacylglycerides, free fatty acids, carbohydrate and heme. Under identical assay conditions, the analogous protein in the soft tick, Ornithodoros parkeri, did not contain heme. CP in the American dog tick consists of two subunits, one of which has 61% identity to the biliprotein, artemocyanin, from the fairy shrimp. CP is identical to a heme-lipoprotein (HeLp) from Boophilus microplus. The exact roles of CP and HeLp have not yet been fully determined, but they apparently are important in heme sequestration and as a storage depot for protein and lipid. Macroglobulin, lectin, antimicrobial, JH binding, JH esterase, and other tick hemolymph proteins are also discussed.

17.
J Insect Physiol ; 48(2): 161-170, 2002 Feb.
Article in English | MEDLINE | ID: mdl-12770115

ABSTRACT

The tissue distribution of the predominant hemolymph protein found throughout tick development was examined in the hard tick, Dermacentor variabilis, and in the soft tick, Ornithodoros parkeri. In D. variabilis, the predominant (purified) hemolymph protein was a lipoglycoheme-carrier protein (DvCP) with a molecular weight of 200K. A protein with a similar mobility on native-PAGE was found in fat body, salivary gland, muscle and ovary from partially fed females which was most abundant in the plasma and salivary gland. DvCP from plasma, salivary gland and fat body of partially fed females consisted of two subunits on SDS-PAGE (98 and 92K). In replete females, only salivary gland exhibited protein subunits equivalent to hemolymph CP. CP in salivary gland and fat body stained positive for lipids. The concentration of CP in tissues varied between partially fed and replete females, indicating a difference in the expression and/or sequestration of CP during adult development. The predominant hemolymph carrier protein from O. parkeri (OpCP) was purified to homogeneity for the first time and is presumed to have similar functions to CP from D. variabilis. Purified OpCP exhibited a molecular weight of 668K by native-PAGE. Unlike CP from D. variabilis, OpCP was not detected in fat body or salivary gland tissues but occurred abundantly in coxal fluid. By SDS-PAGE, purified hemolymph OpCP consisted of two major subunits (114 and 93K) and a less abundant protein with an apparent molecular weight of 48K. Purified native OpCP was a lipoprotein like DvCP. A spectral analysis of purified OpCP failed to demonstrate the presence of heme like that found for CP from D. variabilis, purified by the same methods. However, plasma from O. parkeri contained heme with a lambda(max) of 410nm.

18.
Insect Biochem Mol Biol ; 31(9): 857-65, 2001 Jul 26.
Article in English | MEDLINE | ID: mdl-11439245

ABSTRACT

Hemolymph from partially fed virgin Dermacentor variabilis females was collected following Borrelia burgdorferi challenge and assayed for antimicrobial activity against Bacillus subtilis and B. burgdorferi. A small inducible cationic peptide was identified by SDS-PAGE in the hemolymph of these ticks as early as 1h post challenge. Following purification by a three-step procedure involving sequential SepPak elution, reversed phase high performance liquid chromatography (RP-HPLC) and gel electrophoresis, the yield of the active peptide was approximately 0.1% of the total protein in the hemolymph plasma. The molecular weight, 4.2kDa, was determined by MALDI-TOF mass spectrometry. N-terminal sequencing by the Edman degradation method gave a sequence for the first 30 amino acids as: G-F-G-C-P-L-N-Q-G-A-C-H-N-H-C-R-S-I-(R)-(R)-(R)-G-G-Y-C-S-Q-I-I-K. A computer search of databases showed that the peptide had 83% similarity to a defensin found in a scorpion. This is the first report of a defensin from a tick. The peptide was stable at least up to 70 degrees C. Although the tick defensin alone was not immediately effective against B. burgdorferi, tick defensin plus lysozyme killed more than 65% of cultured B. burgdorferi within 1h.


Subject(s)
Anti-Bacterial Agents/analysis , Defensins/analysis , Dermacentor/chemistry , Amino Acid Sequence , Animals , Bacillus subtilis/immunology , Borrelia burgdorferi Group/immunology , Dermacentor/immunology , Dermacentor/microbiology , Female , Hemolymph/chemistry , Molecular Sequence Data , Peptides
19.
J Med Entomol ; 38(1): 99-107, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11268698

ABSTRACT

The blacklegged tick, Ixodes scapularis Say, transmits the Lyme disease spirochete Borrelia burgdorferi, whereas the American dog tick, Dermacentor variabilis (Say), is unable to transmit the bacterium. We compared the innate immune response of these ticks against spirochetes directly inoculated into the hemocoel cavity of ticks. In I. scapularis, some Borrelia were found associated with hemocytes, while numerous other spiral-shaped, intact bacteria remained free in the hemolymph. In contrast, in D. variabilis only remnants of the bacteria were evident in the hemolymph, indicating lysis; intact spirochetes were rare. Spirochetes were observed bound to or within the organs of both tick species, although many more spirochetes were found associated with the I. scapularis organs. The few spirochetes observed with the D. variabilis organs appeared to be dead because D. variabilis tissues rarely contained culturable bacteria, unlike I. scapularis tissues. When spirochetes were incubated with I. scapularis hemolymph plasma in vitro, bacterial survival and motility were not reduced. In contrast, incubation of spirochetes with D. variabilis hemolymph plasma resulted in > 50% of the spirochetes becoming nonmotile by 45 min. The differences in the responses of the two different tick species indicate that I. scapularis is immunotolerant when challenged with B. burgdorferi and dependent on a slow phagocytic response to clear Borrelia from the hemolymph. In contrast, D. variabilis is highly immunocompetent (i.e., innate immunity), using plasma borreliacidal factors and a rapid increase in phagocytic cells to clear the infection and limit tissue invasion.


Subject(s)
Borrelia burgdorferi Group/immunology , Dermacentor/immunology , Ixodes/immunology , Animals , Cell Count , Dermacentor/microbiology , Female , Hemocytes , Hemolymph , Immune Tolerance , Immunity, Innate , Immunocompetence , Ixodes/microbiology , Rabbits , Rats
20.
Insect Biochem Mol Biol ; 31(4-5): 299-311, 2001 Mar 15.
Article in English | MEDLINE | ID: mdl-11222939

ABSTRACT

A novel lipoglycoheme-carrier protein (CP) in the American dog tick, Dermacentor variabilis (Say) has been purified and characterized. CP was purified by native-PAGE from partially fed virgin females. CP has a density of 1.25 g/ml with a molecular weight of 200 K by native-PAGE and 340 K by gel filtration chromatography. CP is comprised of two majour subunits, 98 K and 92 K in molecular weight by SDS-PAGE. Separate amino acid composition of the two subunits indicated high contents of As(x), Gl(x) and leucine. However, the N-terminal amino acid sequence of the two subunits was only 13% identical. The lower molecular weight subunit showed 61% identity to artemocyanin (biliprotein) in fairy shrimps, 46% identity to minor vitellogenin in chickens and 13% identity to vitellin of the black-legged tick. No similarity match was found for the other subunit. CP is a lipoglycoheme-protein as indicated by selective staining of native-PAGE gel for lipids, carbohydrates and heme. Lipid analysis by thin layer chromatography revealed the presence of cholesterol, phospholipids, monoacylglycerides, triacylglycerides and free fatty acids. Heme associated with purified CP demonstrated a lambda(max) of 397.5 nm while the lambda(max) of crude hemolymph plasma was 402.5 nm. The presence of CP in whole body homogenates of eggs, unfed and fed larvae and fed nymphs as well as in the plasma of unfed and fed adults including vitellogenic females was demonstrated by native-PAGE. Although a protein of analogous size was not found in the soft tick, Ornithodoros parkeri Cooley, a high molecular weight protein (500 K) is the predominant plasma protein in both unfed and fed male and female adults of that species as determined by native-PAGE. Also, CP appears to function as a biliprotein which sequesters heme.


Subject(s)
Acari/chemistry , Dermacentor/chemistry , Hemolymph/chemistry , Acari/growth & development , Amino Acid Sequence , Animals , Carbohydrates/analysis , Dermacentor/growth & development , Dogs , Female , Glycoproteins , Heme/analysis , Hemeproteins , Lipids/analysis , Male , Molecular Sequence Data
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