Tsifoks — user, application, feedback
- 1 Tsifoks
- 2 Structure and Composition Tsifoksa
- 3 General properties Tsifoksa
- 4 Appointment Tsifoksa
- 5 Instructions for use Tsifoksa
- 6 precautionary measures
- 7 First aid for poisoning Tsifoksom
- 8 storage conditions
- 9 Control of tick infestations and pathogen prevalence in cattle and sheep farms vaccinated with the recombinant Subolesin-Major Surface Protein 1a chimeric antigen
- 10 Abstract
- 11 Background
- 12 Methods
- 12.1 Experimental design and rationale
- 12.2 Study site
- 12.3 Vaccine preparation and vaccination
- 12.4 Sample collection
- 12.5 Characterization of tick infestations
- 12.6 Pathogen DNA identification by PCR
- 12.7 Serological analyses
- 12.8 PCR amplification and sequencing of A. marginale and A. ovis major surface protein 4 (msp4) gene
- 13 Results and Discussion
- 13.1 Antibody response in cattle and sheep vaccinated with the SUB-MSP1a antigen
- 13.2 Effect of vaccination on tick infestations on cattle and sheep
- 13.3 Effect of vaccination on the prevalence of tick-borne pathogens
- 13.4 Characterization of the A. marginale and A. ovis msp4 genotypes in cattle and sheep
- 14 Conclusions
- 15 References
Tsifoks — insektoakaritsidny concentrate. This tool is intended for employees of organizations entitled to carry out disinfection measures.
Structure and Composition Tsifoksa
According to the instructions Tsifoks issued in the form of a transparent liquid in plastic bottles.
The composition includes Tsifoksa tsidermetrin (25%), solvents, emulsifiers, perfume. Tsidermetrin — the main active component Tsifoksa.
General properties Tsifoksa
According to the instructions Tsifoks has insektoakaritsidnoe action, ensuring the complete destruction of ants, cockroaches, fleas, bedbugs, scabies and rat mites, larvae and adult mosquitoes and flies, lice, for 20-25 minutes. Duration Tsifoksa depends on the type of surface to be treated and the concentration of the emulsion (from one week to three months). The term residual Tsifoksa on surfaces in rooms ranging from one to three months; in an aqueous medium — 1-3 weeks; in open nature (when used to control Tsifoksa components midges) — from one to six weeks; by treatment of ticks — one to two months. As a result, the garment contact ticks are killed, and the acaricidal effect Tsifoksa persist up to two weeks.
The feedback to the Tsifoksu confirmed that the efficacy of the drug depends on the sensitivity of the population of arthropods to its active component.
In some reviews to Tsifoksu it says that when you use to fight the insect populations and possesses a strong resistance peritroidam his insektoakaritsidnoe effect is greatly reduced.
- elimination of synanthropic insects — bed bugs, cockroaches, ants, fleas, flies and ticks rat;
- disinfestation facilities in the centers of lice and scabies lice and scabies mites;
- disinfestation facilities in the metro and rail transport;
- struggle with the various components of midges in the wild — in the processing of natural and artificial stagnant ponds temporary or permanent existence, areas of land covered by vegetation, buildings and structures. Application Tsifoksa strictly forbidden in waters of economic purpose, used for breeding poultry and fish.
- fight against ticks — carriers of Lyme disease pathogens of encephalitis, tick-borne borreliosis and other diseases (processing of natural habitats).
Instructions for use Tsifoksa
Working emulsion agents should be prepared immediately before use Tsifoksa. Tsifoks be diluted with tap water, continuously stirring the solution for five minutes. Final emulsion should be used within eight hours. For application Tsifoksa often use mnogolitrazhnye globular sprayers. For the destruction of the rat, scabies mites, ants, bed bugs apply 0, 05% aqueous emulsion Tsifoksa. To control cockroaches, fleas, flies, mosquitoes and their larvae using 0 1% aqueous solution of agent.
Emulsion Preparation and filling containers must be carried in special refueling stations. Work with Tsifoksom of instructions is prohibited to persons under 18 years of age, breastfeeding and pregnant women, and persons with hypersensitivity to pesticides. In the workplace it is forbidden to smoke, drink, eat.
Those working with Tsifoksom necessarily be provided with personal protective equipment — protective clothing (antistatic, water repellent or dense tissue), airtight goggles and a respirator. After work, wash exposed areas with water.
Disinsection of premises should be carried out with the windows open, windows. After work, ventilate the room for half an hour. Janitorial at the open window and the windows should be carried out 9-12 hours after delousing.
First aid for poisoning Tsifoksom
Reviews Tsifokse indicate that in cases of poisoning by the tool appear headache, weakness, vomiting, bad taste in mouth, nausea, aggravated by smoking or when eating, profuse salivation, irritation of the respiratory organs. When these symptoms should immediately remove contaminated clothing and rinse your mouth with 2% solution of baking soda or water.
In case of accidental ingestion Tsifoksa need to drink 2-3 glasses of water and induce vomiting. This is followed by a drink one or two glasses of water with activated charcoal 10-20 tablets.
In case of contact with eyes Tsifoksa or skin, rinse immediately with water, or contaminated sites 2% solution of baking soda.
Means Tsifoks flammable! Keep Tsifoks be in special warehouses in a tightly closed container, away from heat and fire, separate from drugs and foods. On capacity have to be a sticker, which indicates the name of the drug, date of manufacture, expiry date.
Working emulsion can not be stored and must be used within eight hours of dilution.
Control of tick infestations and pathogen prevalence in cattle and sheep farms vaccinated with the recombinant Subolesin-Major Surface Protein 1a chimeric antigen
Despite the use of chemical acaricides, tick infestations continue to affect animal health and production worldwide. Tick vaccines have been proposed as a cost-effective and environmentally friendly alternative for tick control. Vaccination with the candidate tick protective antigen, Subolesin (SUB), has been shown experimentally to be effective in controlling vector infestations and pathogen infection. Furthermore, Escherichia coli membranes containing the chimeric antigen composed of SUB fused to Anaplasma marginale Major Surface Protein 1a (MSP1a) (SUB-MSP1a) were produced using a simple low-cost process and proved to be effective for the control of cattle tick, Rhipicephalus (Boophilus) microplus and R. annulatus infestations in pen trials. In this research, field trials were conducted to characterize the effect of vaccination with SUB-MSP1a on tick infestations and the prevalence of tick-borne pathogens in a randomized controlled prospective study.
Two cattle and two sheep farms with similar geographical locations and production characteristics were randomly assigned to control and vaccinated groups. Ticks were collected, counted, weighed and classified and the prevalence of tick-borne pathogens at the DNA and serological levels were followed for one year prior to and 9 months after vaccination.
Both cattle and sheep developed antibodies against SUB in response to vaccination. The main effect of the vaccine in cattle was the 8-fold reduction in the percent of infested animals while vaccination in sheep reduced tick infestations by 63%. Female tick weight was 32-55% lower in ticks collected from both vaccinated cattle and sheep when compared to controls. The seroprevalence of Babesia bigemina was lower by 30% in vaccinated cattle, suggesting a possible role for the vaccine in decreasing the prevalence of this tick-borne pathogen. The effect of the vaccine in reducing the frequency of one A. marginale msp4 genotype probably reflected the reduction in the prevalence of a tick-transmitted strain as a result of the reduction in the percent of tick-infested cattle.
These data provide evidence of the dual effect of a SUB-based vaccine for controlling tick infestations and pathogen infection/transmission and provide additional support for the use of the SUB-MSP1a vaccine for tick control in cattle and sheep.
Tick infestations affect animal health and production worldwide, both for the impact on animal weight gain and milk production and for the pathogens transmitted by these ectoparasites [1–4]. Acaricides are a major component of integrated tick control strategies, but their application has had limited efficacy in reducing tick infestations and is often accompanied by serious drawbacks, including the selection of acaricide-resistant ticks, environmental contamination and contamination of milk and meat products with drug residues . All of these issues reinforce the need for alternative approaches to control tick infestations and pathogen transmission, including the use of vaccines with tick antigens [5–7].
In the early 1990s, commercial vaccines containing the recombinant Rhipicephalus (Boophilus) microplus BM86 gut antigen were developed and commercialized for the control of cattle tick infestations . These vaccines proved to be a cost-effective alternative for cattle tick control through the reduction of the number of engorged female ticks, their weight and reproductive capacity and the prevalence of some tick-borne pathogens [1, 8]. However, BM86-based vaccines have limited efficacy against other tick species and thus new vaccines are needed for the control of multiple tick species infestations, which occur in many areas used for animal husbandry [5, 6, 8].
Recently, Subolesin (SUB) was discovered as a new candidate tick protective antigen [9, 10]. Vaccination trials with recombinant SUB and its ortholog in insects, Akirin, demonstrated effective control of arthropod vector infestations in various hard and soft tick species, mosquitoes, sand flies, poultry red mites and sea lice by reducing their numbers, weight, oviposition, fertility and/or molting and also reduced tick infection with tick-borne pathogens, Anaplasma phagocytophilum, Anaplasma marginale, Babesia bigemina and Borrelia burgdorferi. Furthermore, the chimeric antigen, tick SUB fused with A. marginale Major Surface Protein 1a (MSP1a; SUB-MSP1a), was produced in Escherichia coli using a simple and low-cost process. Use of a vaccine with bacterial membranes containing the SUB-MSP1a chimera with surface-exposed SUB provided control of R. microplus and R. annulatus tick infestations [12, 13], and this vaccine formulation was proposed as a low-cost and effective alternative means of tick control.
However, vaccination trials with SUB-MSP1a were conducted under controlled conditions and only in cattle experimentally infested with R. microplus and R. annulatus, which limit the assessment of the potential impact of this vaccine for the control of tick infestations and the prevalence of tick-borne pathogens under field conditions. To address these limitations, herein we conducted field trials on cattle and sheep farms in order to assess the efficacy of the SUB-MSP1a vaccine for the control of multiple tick species and tick-borne pathogens.
Experimental design and rationale
The field trial was designed to characterize the effect of vaccination with SUB-MSP1a on tick infestations and the prevalence of tick-borne pathogens at the DNA and serological levels in a randomized controlled prospective study. Two cattle and two sheep farms with similar geographical locations and production characteristics were randomly assigned as control or vaccinated herds. These farms were followed for one year prior to vaccination and 9 months after vaccination. Vaccine trials were approved by the Italian Ministry of Health (Direzione Generale della Sanita’ Aimale e dei Farmaci Veterinari, permit no. DGSAF 0002336-P-08/02/2011).
Two cattle farms (identified as G for vaccinated and M for control) and two sheep farms (identified as C for vaccinated and L for control) located in the Province of Palermo, Sicily, were included in the trial (Figure 1). Cattle farms had a similar location (G, 38.00738 and 13.25156; M, 38.03039 and 13.23532), altitude (G, 950 m; M, 700 m), and number of animals (G, N = 35; M, N = 31). Sheep farms also had a similar location (C, 38.02188 and 12.98748; L, 38.03482 and 13.08531), altitude (C, 150 m; L, 175 m), and number of animals (C, N = 133; L, N = 123). Land use was also similar between cattle and sheep farms (Figure 1).
Localization of cattle and sheep farms and land use in the study area. Maps were constructed using the Esri ArcMap 9.3 software. (A) Localization of the study area in the Province of Palermo, Sicily. The digital elevation model was processed through the interpolation of level curves values of the Sicilian region, obtaining the elevations of study sites. (B) The land use of the areas near to the farms was obtained from Corine Land Cover 2006 processed by the European Environmental Agency describing the coverage and, in part, the use of the soil in Europe. Spatial selection allowed deriving the different levels of the land use classes that affect the areas where the farms are placed. (C) The analysis showed that vaccinated and control sheep (L and C) and cattle (M and G) farms are located close to each other in the same region and have similar land use.
Vaccine preparation and vaccination
Unless otherwise indicated, all reagents used in this work were purchased either from Sigma-Aldrich (St Louis, MO, USA) or VWR International Eurolab S.L. (Mollet del Vallés, Barcelona, Spain). The vaccine containing bacterial membranes with surface-exposed R. microplus SUB-MSP1a chimeric antigens was prepared as previously described . Briefly, recombinant E. coli JM109 cells transformed with the pMBXAF3 expression vector were propagated in 1 litre flasks containing 250 ml Luria–Bertani (LB) broth supplemented with 10 g/l tryptone, 5 g/l yeast extract, 10 g/l NaCl, 50 μg/ml ampicillin and 0.4% glucose (Laboratorios CONDA S.A., Madrid, Spain) for 2 h at 37ºC and 200 rpm and then for 5.5 h after addition of 0.5 mM final concentration of isopropyl-β-d-thiogalactopyranoside (IPTG) for induction of recombinant protein production . The cells were harvested by centrifugation at 10,000 x g for 15 min at 4ºC and then 1 g of cell pellet was resuspended in 5 ml of disruption buffer (100 mM Tris HCl, pH 7.5, 150 mM NaCl, 1 mM PMSF, 5 mM MgCl2 · 6H2O and 0.1% (v/v) Triton X-100) and disrupted using a cell sonicator (Model MS73; Bandelin Sonopuls, Berlin, Germany). After disruption, the insoluble protein fraction containing the membrane-bound SUB-MSP1a was collected by centrifugation at 21, 500 x g for 15 min at 4°C. The membrane-bound insoluble protein fraction containing over 50% of total proteins corresponding to the SUB-MSP1a chimera was resuspended in PBS, pH 7.4 and adjuvated in Montanide ISA 50 V2 (Seppic, Paris, France) at a concentration of 125 μg/ml.
All cattle and sheep present in the farms, including newborns at month 4 of age and adults imported during the trial were treated. Animals in cattle farm G and sheep farm C were vaccinated with two immunization doses of 1 ml containing 100 μg of the antigen preparation. Animals in cattle farm M and sheep farm L were injected with a similar volume of adjuvant/saline alone as control. Injections were done intramuscularly in the back of the animals using a 2.5-ml syringe and an 18G needle. Cattle in vaccinated and control farms were vaccinated or injected with adjuvant/saline on March 19 th and April 20 th , 2012. Sheep in vaccinated and control farms were vaccinated or injected with adjuvant/saline on March 13 th and April 12 th , 2012. Cattle in both vaccinated and control farms were treated with tilmicocin to prevent pneumonia prior to the first vaccination or adjuvant/saline injection following the manufacturer’s recommendations (TILMI-kel; KELA Laboratoria, Hoogstraten, Belgium). No contraindications have been described for this or similar products with respect to response to vaccination.
In each farm, ticks and EDTA-treated and untreated blood samples were collected from all animals before each immunization and four weeks after the last immunization and then monthly from randomly selected individuals representing 10% of the animals present in the farm. Serum was separated from blood samples by centrifugation and stored with EDTA-treated blood samples at −20°C.
Characterization of tick infestations
Collected ticks were counted for each animal, identified by morphological features using standard taxonomic keys for Italian Ixodidae  and preserved in 70% ethanol. Replete female ticks were weighed individually and the weights (mg) were compared between animals in the vaccinated farm before and after vaccination and between vaccinated and control farms by Student’s t-test with unequal variance (p = 0.05). Tick infestations (ticks/animal) were modeled separately for cattle and sheep using a generalized lineal model with binomial function and logit error with the dependent variables presence/absence of ticks and sampling time and farm as explanatory variables (p = 0.01; SPSS Statistics version 19, Surrey, UK). Tick infestations (ticks/animal) were compared between vaccinated and control animals using an ANOVA test (p = 0.05). The percent of animals infested with ticks before and after vaccination was compared between vaccinated and control farms by Student’s t-test with unequal variance (p = 0.05).
Pathogen DNA identification by PCR
DNA was extracted from EDTA-treated blood samples using the PureLink Genomic Mini kit (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s instructions. DNA samples were analyzed by PCR as reported previously to detect the presence of DNA from Anaplasma spp.  in all samples and positive samples were then analyzed for A. marginale/A. ovis[17, 18] and A. phagocytophilum DNA. The presence of DNA from A. marginale[17, 18], Babesia bovis, B. bigemina and Theileria annulata was analyzed in cattle only while DNA from A. ovis, B. ovis and T. ovis was characterized in sheep only. Coxiella burnetii and A. phagocytophilum DNA was characterized in both cattle and sheep samples.
PCRs were performed in a reaction buffer containing 1.5 mM MgCl2, 0.2 mM dNTPs, forward and reverse primers at a concentration of 0.4 mM, and 0.025 U/μl of Taq polymerase (5 U/μl) (Promega, Madison, WI, USA). For each reaction, a positive control consisting of pathogen DNA and a negative control in which DNA was replaced by water were used. PCR products were visualized after agarose gel electrophoresis containing 10 μg/ml ethidium bromide. Pathogen DNA prevalence (% positive animals) was compared between animals in the vaccinated farm before and after vaccination and between vaccinated and control farms by Student’s t-test with unequal variance (p = 0.05).
Serum antibody titers were determined using antigen-specific indirect ELISAs against SUB-MSP1a or SUB [12, 25]. Briefly, purified antigens (0.1 μg/well) were used to coat ELISA plates overnight at 4°C. Plates were then washed three times with PBS/0.1% tween 20, pH 7.2. Sera were serially diluted to 1:100 and 1:1000 in PBS/0.5% Tween 20, pH 7.2 (PBST) and 10% fetal bovine serum (Sigma). The plates were incubated with the diluted sera for 1 hr at 37°C, washed three times with PBST and then incubated with 1:10,000 rabbit anti-bovine immunoglubolin G (IgG)-horseradish peroxidase conjugate (Sigma) for 1 hr at 37°C. Plates were washed three times with PBST and the color reaction was developed after incubation at 37°C with 200 μl of the substrate SIGMAFAS™OPD (Sigma). The reaction was stopped after 20 min with a solution of 4N sulphuric acid and the O.D.450nm was determined. Antibody titers were considered positive when they yielded an O.D.450nm value at least twice as high as the preimmune serum. Antibody titers were expressed as the O.D.450nm value for the highest serum dilution (1:1000) and compared between vaccinated and placebo control cattle using an ANOVA test (p = 0.05).
Bovine and ovine serum samples were analyzed using commercial ELISA kits for the presence of antibodies against A. marginale/A. ovis (VMRD, Pullman, WA, USA), B. bigemina (Svanova Biotech AB, Uppsala, Sweden) and C. burnetii (ID.vet, Montpellier, France) following manufacturer’s recommendations. The presence of antibodies against T. annulata was evaluated by immunofluorescence using antigen slides prepared as described previously . Pathogen seroprevalence (% positive animals) was compared between animals in the vaccinated farm before and after vaccination and between vaccinated and control farms by Student’s t-test with unequal variance (p = 0.05).
PCR amplification and sequencing of A. marginale and A. ovis major surface protein 4 (msp4) gene
Total DNA was extracted from EDTA-treated blood samples and analyzed by msp4 PCR as described before  in all samples positive for Anaplasma spp. DNA. The msp4 amplicons were purified using the MinElute PCR Purification Kit (Qiagen, Hilden, Germany) and sequenced (Secugen S.L., Madrid, Spain). Genotype frequencies were calculated as the percent of animals positive for each genotype. A correlation analysis was conducted to analyze genotype frequencies in time using Excel. The msp4 sequences were aligned using the program AlignX (Vector NTI Suite V 5.5, InforMax, North Bethesda, MD, USA). The msp4 sequences were submitted to the GenBank under accession numbers [GenBank: KF739427-KF739433].
Results and Discussion
Antibody response in cattle and sheep vaccinated with the SUB-MSP1a antigen
Cattle and sheep from vaccinated herds developed antibodies against SUB-MSP1a after vaccination, reaching a peak one month after the last immunization (Figure 2A and B). Significantly higher antibody titers against the vaccine antigen, SUB-MSP1a (Figure 2A and B) or recombinant SUB [Additional file 1: Figures S1 and S2] persisted in vaccinated animals for three months after the last immunization when compared to control animals. These results were similar to those previously obtained in cattle vaccinated with SUB-MSP1a . Antibody titers to MSP1a were not determined because they are irrelevant for the studies reported here in part because antibodies in livestock persistently infected with Anaplasma react with MSP1a, which would preclude assessment of the humoral response to this part of the antigen after vaccination.
Effect of vaccination on tick infestations on cattle and sheep
One of the effects of SUB-MSP1a and other tick vaccines is the reduction in tick infestations [5, 8, 10, 12]. The tick infestation rate (ticks/animal) was very low in the year before vaccination with no differences between cattle farms (Figure 3A; generalized lineal model, p = 0.3) but did differ between sheep farms with higher tick infestations in farm C (Figure 3B; generalized lineal model, p Figure 3
Ticks collected on vaccinated and control animals throughout the experiment were classified and included Hyalomma lusitanicum, Haemaphisalis punctata, Rhipicephalus bursa, Rhipicephalus sanguineus, Rhipicephalus turanicus, Rhipicephalus annulatus and Ixodes ricinus in cattle, and Dermacentor marginatus, R. sanguineus, R. turanicus and Haemaphisalis sulcata in sheep. To address the differences between ticks infesting cattle and sheep, ticks were grouped according to their genera (Figure 4A-D). Hyalomma spp., followed by Rhipicephalus spp. and Haemaphysalis spp. were the predominant tick species found on cattle (Figure 4A and B). However, the predominant tick species infesting sheep were Rhipicephalus spp. followed by Haemaphysalis spp. and Dermacentor spp. (Figure 4C and D). These tick species are among the most abundant species found in the study area and the results reflect differences between preferred hosts for these species [27, 28].
Tick species infesting cattle and sheep. Ticks collected from (A, B) cattle and (C, D) sheep in both (A, C) vaccinated and (B, D) control farms were classified, grouped according to tick genera and represented as percent of total ticks collected throughout the experiment.
The tick infestation rate was then characterized for the most abundant tick species infesting cattle (Figure 5A-C) and sheep (Figure 5D-F). The appearance of the infestation peak varied between tick species reflecting variations in developmental seasonality for ticks . In cattle, only Haemaphysalis spp. infestations were lower in vaccinated animals after vaccination (Figure 5C) while in sheep only Dermacentor spp. infestations were lower in vaccinated animals after vaccination (Figure 5D). Interestingly, Rhipicephalus spp. infestations were higher or similar in vaccinated cattle and sheep, respectively when compared to control animals (Figure 5B and E). At first, these results suggested a contradiction with previous experiments in which the SUB-MSP1a vaccine was protective against R. microplus and R. annulatus infestations in cattle . However, the most abundant Rhipicephalus spp. collected from infested animals in this trial corresponded to R. bursa, R. sanguineus and R. turanicus in cattle and R. sanguineus and R. turanicus in sheep. These results suggested that the efficacy of the SUB-MSP1a vaccine differs between cattle and sheep and between different tick species (Figure 5A-F).
Previous results with the SUB-MSP1a vaccine showed that vaccination not only reduced cattle tick infestations but also the weight of replete female ticks . Additionally, field application of BM86-based commercial vaccines showed a reduction in the percent of infested cattle . Therefore, the effect of the vaccine was characterized on the weight of female ticks collected from cattle and sheep and the percent of infested animals in both control and vaccinated farms. The results showed Hyalomma spp. and Haemaphysalis spp. but not Rhipicephalus spp. female ticks collected from vaccinated cattle had significantly 32-39% lower weights when compared to the same animals before vaccination and to control cattle (Figure 6A). Furthermore, the percent of infested cattle was higher before vaccination but lower after vaccination in the vaccinated farm at some time points when compared to control animals (Figure 6B). The analysis of the number of infested cattle before and after vaccination showed that while the percent of infested animals was significantly higher in cattle in the vaccinated farm when compared to control cattle before vaccination, differences were not observed after vaccination between vaccinated and control cattle but only in the control farm before and after vaccination (Figure 6C). These results showed that vaccination with SUB-MSP1a maintained a similar percent of infested cattle after vaccination while in the control farm the percent of infested animals increased in more than 8-fold in the second year of the trial (Figure 6D).
In sheep, 43-55% reduction in female tick weight was recorded for Rhipicephalus sp. and Haemaphysalis spp. collected from vaccinated animals when compared to the same animals before vaccination and to control sheep (Figure 7A). However, the percent of infested sheep was not affected by vaccination with SUB-MSP1a (Figure 7B-D).
Taken together, these results showed that the main effect of the SUB-MSP1a vaccine in cattle was the reduction in the percent of infested animals but not in the tick infestation rate of these animals. On the contrary, vaccination in sheep did not affect the percent of infested animals but reduced tick infestations. The reduction of female tick weight was observed in ticks collected from both vaccinated cattle and sheep.
Effect of vaccination on the prevalence of tick-borne pathogens
The ultimate goal of tick vaccines is to reduce the prevalence of tick-borne diseases . Tick vaccines have been shown to reduce the prevalence of tick-borne pathogens by reducing tick infestations and thus the exposure of susceptible hosts to pathogen transmission (e.g. BM86-based vaccine; ) and through reduction of tick vector capacity (e.g. SUB; [10, 11]). Importantly, vaccination with SUB has shown that the vaccine reduces both tick infestations and pathogen infection/transmission, thus having a dual effect on reducing tick-borne diseases [11, 29].
In our trial, the prevalence of tick-borne pathogens that has been described infecting cattle and/or sheep in Sicily [28, 30–33] was analyzed at the DNA (A. marginale, A. ovis, A. phagocytophilum, B. bovis, B. bigemina, B. ovis, T. annulata, T. ovis and C. burnetii) and serology (Anaplasma spp., B. bigemina, T. annulata and C. burnetii) levels. The prevalence of A. marginale, B. bovis, B. bigemina and T. annulata was analyzed in cattle only while the prevalence of A. ovis, B. ovis and T. ovis was characterized in sheep only. C. burnetii and A. phagocytophilum prevalence were characterized in both cattle and sheep.
The results showed less than 1% DNA prevalence in both vaccinated and control cattle throughout the period of the trial for A. phagocytophilum, B. bigemina, B. bovis and C. burnetii (data not shown). However, B. bigemina seroprevalence decreased by 30% in vaccinated cattle after vaccination when compared to controls (Figure 8A), suggesting a role for the vaccine in reducing pathogen transmission. As expected for animals that develop persistent infection, the seroprevalence for Anaplasma spp. was higher than 90% throughout the experiment and did not change between vaccinated and control cattle nor before and after vaccination [Additional file 1: Figure S5]. For A. marginale DNA prevalence, the results showed an increase after vaccination but with similar levels for vaccinated and control cattle (Figure 8B). The seroprevalence for C. burnetii was less than 1% in cattle farm G throughout the experiment, while peaks of positive antibodies were observed in farm M but did not differ between vaccinated and control cattle nor before and after vaccination [Additional file 1: Figure S6]. The prevalence of T. annulata DNA increased after vaccination in control but not in vaccinated cattle but did not differ between vaccinated and control animals (Figure 8C). Similarly, T. annulata seroprevalence was high until the end of the experiment and did not differ between vaccinated and control cattle throughout the experiment [Additional file 1: Figure S7].
In sheep, less than 1% DNA prevalence was observed for A. phagocytophilum, B. ovis and C. burnetii in both vaccinated and control animals throughout the experiment (data not shown). The seroprevalence for Anaplasma spp. was higher in control than in vaccinated sheep but both before and after vaccination (Figure 9A). C. burnetii seroprevalence was also higher in control than in vaccinated sheep but decreased by 37% in vaccinated sheep after vaccination (Figure 9B). In agreement with serological results, A. ovis DNA prevalence was higher in control than in vaccinated sheep but both before and after vaccination (Figure 9C). The prevalence of T. ovis DNA was high throughout the experiment with no differences between vaccinated and control sheep [Additional file 1: Figure S8].
In summary, the results of vaccination with SUB-MSP1a on the prevalence of tick-borne pathogens suggested a role for the vaccine in decreasing B. bigemina seroprevalence in cattle. This finding is in agreement with the results of previous studies and demonstrated that vaccination with SUB reduces B. bigemina DNA levels in ticks fed on infected and vaccinated cattle [25, 29]. Additionally, this result may reflect the reduction in the percent of infested animals shown in cattle vaccinated with SUB-MSP1a. However, in contrast to previous results in cattle vaccinated with SUB [25, 29], vaccination with SUB-MSP1a did not reduce the prevalence for A. marginale. In sheep, the only effect of the vaccine was on the decrease of C. burnetii seroprevalence in vaccinated but not in control animals after vaccination. However, this result may reflect better farm management and animal health conditions in sheep farm C when compared to farm L, factors known to affect the prevalence of C. burnetii[34, 35] and other tick-borne pathogens . As shown in field trials using BM86-based commercial vaccines , the reduction in tick infestations in sheep vaccinated with SUB-MSP1a would require several years of vaccination before it could decrease the prevalence of some tick-borne pathogens.
Characterization of the A. marginale and A. ovis msp4 genotypes in cattle and sheep
A. marginale and A. ovis are transmitted not only biologically by ticks, but also mechanically by biting insects and blood contaminated fomites . Therefore, despite the fact that vaccination with SUB-MSP1a did not affect Anaplasma spp. prevalence in this trial, we characterized A. marginale and A. ovis msp4 genotypes trying to identify a possible effect of the vaccine on some genotypes likely transmitted by ticks. For this analysis, we used the msp4 genetic marker, which has been used before for the characterization of genetic diversity in these species .
The results showed a high genetic diversity for A. marginale in cattle (11 msp4 genotypes; Figure 10A-C), a finding common to cattle herds in Sicily  and other regions of the world [39, 40]. Genotype frequencies were different between vaccinated and control farms and between samples collected before and after vaccination (Figure 10A and B). Interestingly, the analysis of the most frequent genotypes showed an effect of cattle vaccination with SUB-MSP1a on decreasing the frequency for genotype AmA, but not for AmE and AmH genotypes (Figure 10D). These results suggested an effect of the vaccine in reducing the frequency for A. marginale genotype AmA, probably reflecting the reduction in the percent of tick-infested animals shown in cattle vaccinated with SUB-MSP1a that reduces the prevalence of a tick-transmitted strain. As in previous studies [39, 41], the genetic diversity for A. ovis (4 msp4 genotypes) was lower when compared to A. marginale (Figure 11A-C). Differences were not observed in A. ovis msp4 genotype frequency between vaccinated and control sheep nor before and after vaccination with SUB-MSP1a (Figure 11A and B).
Characterization of the A. marginale msp4 genotypes in cattle. The A. marginale msp4 coding region was amplified by PCR, sequenced and the frequency (%) for each genotype represented in (A) vaccinated and (B) control cattle. Dashed line represents time of last immunization shot. (C) The msp4 sequences of each genotype were aligned and compared to the reference sequence (GenBank accession number DQ000618). Sequence positions (the adenine in the translation initiation codon ATG corresponds to position 1) with polymorphisms were identified. Asterisks represent sequence positions identical to the reference sequence. (D) Distribution in the frequencies of the most abundant A. marginale msp4 genotypes in vaccinated and control cattle. Dashed line represents time of last immunization shot. A correlation analysis was conducted to analyze genotype frequencies in time using Excel and represented only when the correlation coefficient (R 2 ) was ≥0.5.
Characterization of the A. ovis msp4 genotypes in sheep. The A. ovis msp4 coding region was amplified by PCR, sequenced and the frequency (%) for each genotype represented in (A) vaccinated and (B) control sheep. Dashed line represents time of last immunization shot. A correlation analysis was conducted to analyze genotype frequencies in time using Excel and represented only when the correlation coefficient (R 2 ) was ≥0.5. (C) The msp4 sequences of each genotype were aligned and compared to the reference sequence (GenBank accession number EU436160). Sequence positions (the adenine in the translation initiation codon ATG corresponds to position 1) with polymorphisms were identified. Asterisks represent sequence positions identical to the reference sequence.
To our knowledge, this is the first vaccine trial assessing the control of multiple tick species infestations and pathogen prevalence in cattle and sheep and the first field trial using the SUB-MSP1a vaccine. The main findings of these studies were that (a) both cattle and sheep developed antibodies in response to vaccination; (b) the main effect of the vaccine in cattle was the reduction in the percent of infested animals but not in the tick infestation rate in these animals; (c) vaccination in sheep did not affect the percent of infested animals but reduced tick infestations; (d) female tick weight was lower in ticks collected from both vaccinated cattle and sheep when compared to controls; (e) lower B. bigemina seroprevalence in vaccinated cattle suggested a role for the vaccine in decreasing the prevalence of this tick-borne pathogen; and (f) the effect of the vaccine in reducing the frequency of one A. marginale genotype probably reflected the reduction in the prevalence of a tick-transmitted strain as a result of the reduction in the percent of tick-infested cattle. The lower female tick weights are likely to impact and decrease tick populations over time because it has been well documented that lower female tick engorgement weights correlate with the oviposition of smaller egg masses. This trend would likely reduce tick populations over time. As has been noted previously, tick vaccines are likely to be an important component of integrated tick control methods and would likely reduce the use of acaricides.
These results provide new evidence to support that SUB-based vaccines have the dual effect of controlling tick infestations and pathogen infection/transmission, thus reducing tick populations and their vector capacity to impact on the control of tick-borne diseases . These results also provide additional support for the use of the vaccine containing E. coli membranes with the surface-exposed SUB-MSP1a chimera as a low-cost and effective alternative for tick control in cattle and sheep, even under conditions with multiple tick species infestations and the prevalence of several tick-borne pathogens.
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