ANALYSES OF HEMOLYMPH FROM AMBLYOMMA CAJENNENSE (ACARI: IXODIDAE) USING NAA



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2011 International Nuclear Atlantic Conference - INAC 2011 Belo Horizonte,MG, Brazil, October 24-28, 2011 ASSOCIAÇÃO BRASILEIRA DE ENERGIA NUCLEAR - ABEN ISBN: 978-85-99141-04-5 ANALYSES OF HEMOLYMPH FROM AMBLYOMMA CAJENNENSE (ACARI: IXODIDAE) USING NAA Simone M. Simons 1, Daniella G. L. Oliveira 1, Ana M. Chudzinski-Tavassi 1 and Cibele B. Zamboni 2 1 Instituto Butantan, São Paulo, Brasil Av. Vital Brasil 1500 05503-900, São Paulo, SP simomsimons@yahoo.com.br daniellaoliveira@butantan.gov.br amchudzinki@butanatn.gov.br 2 Instituto de Pesquisas Energéticas e Nucleares, IPEN - CNEN/SP, Brasil Av. Professor Lineu Prestes 2242 05508-000 São Paulo, SP czamboni@ipen.br ABSTRACT Instrumental Neutron Activation Analysis technique (INAA) was applied to determine the elemental composition of hemolymph from Amblyomma cajennense tick. This biological material came from Butantan Institute (São Paulo city, Brazil) and it was investigated using the IEA-R1 nuclear reactor (4MW, pool type) at IPEN/CNEN-SP - Brazil. The concentration values for: Br (0.0032 ± 0.0005gL -1 ), Ca (0.104 ± 0.029gL -1 ), Cl (4.41 ± 0.25gL -1 ), I (76 ± 27µgL -1 ), K (0.38 ± 0.09gL -1 ), Mg (0.038± 0.011gL -1 ), Na (4.30 ± 0.26gL -1 ) and S (1.35± 0.37gL -1 ) were determined for the first time. These data were compared with the concentration values established for Americanum and Anatolicum Excavatum tick species to clarify the ion balance in this biological material (hemolymph). This comparison suggests that Na concentration, majority in these species, has a similar behavior. These data also contribute to the understanding of hemolymph composition complementing its characterization as well as for the understanding of several physiological processes, especially those related to salivary secretion. 1. INTRODUCTION The tick Amablyomma cajennense is considered one of the most important and widespread species in Brazil. It belongs to the hard tick s family (Ixodidae), one of the most prevalent species in the Neotropic region [1]. In the last years several investigations have been performed in its salivary secretion. Particularly, in Brazil, the tick Amablyomma cajennense is target of several important research such as, investigations in the biocenology field [2,3], as the vector of diseases [4], as a source for the development of new molecules focusing on anticoagulation (Factor X activate inhibitor, platelet inhibitor) [5,6] and also as antitumor agents [7,8]. Recently, NAA technique was applied to investigate the saliva of this species [9] and now we intend to determine the elemental composition of the hemolymph this specie also using the INAA technique to complement its biochemistry characterization.

2. MATERIAL AND METHODS The biological material came from Butantan Institute (São Paulo city, Brazil). The experiments were carried out in accordance with protocol approved by the Committee of Ethics of the Butantan Institute (548 08). To obtain this body fluid it is necessary to keep a colony of several adult (females/males). For this investigation 30 females and 15 males were infested in domestic rabbits, Oryctolagus cuniculus, to be fed. After two weeks these ticks were removed and the hemolymph was collected. The hemolymph was obtained through a perforation (puncture) in the cuticle Aloscutum using a 30 gauge needle coupled to calibrated capillaries. For this investigation the collection procedure was repeated two times. Samples of 500 µl (in duplicate) were lyophilized and transferred to a polyethylene tube (cylinder). Aliquots of standard solutions were transferred to Whatman filter paper (~1.5 cm 2 ), using a calibrated micropipette, and dried using an infrared lamp. Sample and standard were irradiated in the IEA-R1 nuclear reactor at IPEN/SP (2-4MW, pool type) for short time irradiation, in a thermal neutron flux of 4.8 10 12 n cm -2 s -1, and for long time irradiation in a thermal neutron flux of 8.5 10 12 n cm -2 s -1. Each sample was measured at least twice. For 38 Cl (T 1/2 =37 min, E γ =1642 kev) and 24 Na (T 1/2 =15h, E γ =1368 kev) determination an irradiation time of 1 minutes followed by 4 minutes of counting time was used. For 80 Br (T 1/2 ~ 16 min, E γ = 616 kev), 49 Ca (T 1/2 ~ 9 min, Eγ = 3098 kev), 128 I (T 1/2 ~ 25 min, Eγ = 443 kev), 27 Mg (T 1/2 ~ 9 min, Eγ = 1012 kev), 42 K (T 1/2 ~ 12h, E γ = 1525 kev) and 37 S (T 1/2 = 5 min, E γ = 3104 kev) sample and standard were irradiated for 4 minutes and after a decay time of 1 minute they were counted by 15 minutes for Br, Ca, Mg and S determination followed by 2 hours of counting for I and 3 hours for K. For 59 Fe (T 1/2 ~ 44.5d, E γ =1099 kev and 1291 kev) determination an irradiated for 8 hours, decay time of 4 days followed by 4 hours of counting time was used. 81 Br (T 1/2 ~ 35h, E γ = 776 kev) and 47 Ca (T 1/2 ~ 4.5 d, E γ = 1297 kev) isotopes were also determined by long irradiation time using a decay time of 1 day and counting time of 2h. A γ- spectrometer system with an ORTEC detector (Model GEM-60195, FWHM=1.89 kev), calibrated for energy through the measurements of standard sources of Co 56,60 and Eu 152, coupled to a MCA ORTEC (Model 919E) and connected to a PC, was used to measure the induced gamma-ray activity. The background radiation was reduced by employing the iron shield described by Medeiros et al [10]. The concentrations of the elements were calculated using in-house software [11]. The quality of analytical results was evaluated by analyzing the NIST 8414 Bovine Muscle Powder and IAEA A-13 Animal Blood certified reference materials. The filter paper and polyethylene tube were also analyzed using the same irradiation conditions. 3. RESULTS AND DISCUSSION The accuracy evaluation by Z-score test (Z < 2 ) for NIST 8414 Bovine Muscle Powder and IAEA A-13 animal blood certified reference materials indicate the adequacy of the method. Some impurities such as Al, and Ca, Cl and Na were identified in the filter paper and Mg in the polyethylene tube, but they do not interfere.

The Br, Ca, Cl, I, K, Mg, Na and S concentration values determined in hemolymph samples are presented in Table 1. The mean values with associated error, represented by one standard deviation (1σ), were compared to the values established for A. americanum [12] and H. (a). excavatum (Hyalomama Anatolicum Excavatum) [13] species from Ixodidae tick s family. These comparisons are summarized in Figure 1. Table 1. Elemental concentrations in hemolymph of Amblyomma cajennense specie using INAA. Elements Mean ± 1σ Min Max Confidence Interval (95%) 1.7 4.6 2.2-4.2 Br, mgl -1 3.2 ± 0.5 3.0 ± 0.4 LI Ca, mgl -1 104 ± 29 99 134 46 168 110 ± 29 LI 255 c Cl, gl -1 4.41 ± 0.25 3.64 5.68 3.91 4.91 4.79 ± 0.96 a 2.80 b I, µgl -1 76 ± 27 60 85 22 110 K, gl -1 0.38 ± 0.09 0.32 0.40 0.20 0.56 0.59 ± 0.12 a 0.31 b Mg, mgl -1 38.0 ± 1.1 167 c 30.0 45.1 35.8 40.2 Mn, mgl -1 0.21 ± 0.03 13.6 24.7 0.15 0.27 Na, gl -1 4.30 ± 0.26 4.09 5.13 3.78 4.82 4.23 ± 0.85 a 4.29 b S, gl -1 1.35 ± 0.37 0.78 1.46 0.61 2.09 a data from A. americanum specie [12] b data from H. (a). excavatum specie [13] c data from A. americanum specie [14] LI : long irradiation time min: minimum concentration value determined max: maximum concentration value determined

Figura 1. Concentration proportions between Ixodidae species. A. cajennense A. americanun H. (a) excavatum 100% concentration proportion 75% 50% 25% 0% Na K Cl Ca Mg According to Table 1, the concentration value for Na obtained for A. cajannense (4.30gL -1 ) is in agreement with the A. americanum (4.30gL -1 ) and also with H. (a) excavatum (4.29gL -1 ) species. Then, the high concentration of Na in hemolymph appears to be feature in these Ixodidae species. This behavior was also identified in investigation performed by Rehacek and Brzostowski [15] and by Tatchell [16] in others hard tick s family (Ixodidae). Cl is also majority in this fluid [13,15,16] and its concentration in A. cajannense specie (4.41gL -1 ) is in agreement with data from A. americanum (4.79gL -1 ). Related to K concentration values, there is a better agreement between results from A. cajannense (0.38gL -1 ) and H. (a) excavatum (0.31gL -1 ) species. For Ca and Mg the concentration results can be only compared with A. americanum species but they are quite different. All these comparisons are summarized in Figure 1. Br and Ca were determined by short and long irradiation time and the results were included in Table 1. Related to Fe, although it has been identified, it was not quantified due the quantity of biological material available was not enough to produce good statistics. The comparative analyses of hemolymph from species (A. cajannense, A. americanum and H. (a) excavatum) suggest that Na, K and Cl concentrations have a similar behavior. 4. CONCLUSIONS

For the first time NAA technique was applied to determine elemental composition (Br, Ca, Cl, I, K, Mg, Mn, Na and S) in hemolymph from Amblyomma cajennense tick. These data contribute to the understanding of it hemolymph composition, complementing its characterization, and adding expertise in several research areas such as formulation of vaccine as well as therapeutic targets. ACKNOWLEDGMENTS The authors thank the financial support of Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). REFERENCES 1. A Estrada-Peña, J M Venzal, D González-Acuña, A A Guglielmone Estado actual del conocimento de las garrapatas (Acari: Ixodoidea) en Chile J Med Entomol 40(6):766-769(2003). 2. R R Cabrera, M B Labruna Influence of photoperiod and temperature on the larval behavioral diapause of Amblyomma cajennense (Acari: Ixodidae) J Med Entomol 46:1303-1309(2009). 3. M B Labruna, F A Terassini, L M Camargo, Notes on population dynamics of Amblyomma ticks (Acari: Ixodidae) in Brazil J Parasitol 95:1016-1018(2009). 4. M B Labruna, Ann N Y Acad Sci 1166:156-166(2009). 5. M S Simons e A M Chudzinski-Tavassi. (2006). Inibidores da coagulação sangüínea e da agregação plaquetária presentes na saliva de carrapatos In: D M Barros-Battesti, D.M Arzua; G H Bechara. (Eds). Vox/ICTTD-3/Butantan, SP, Brazil. 6. S M. Simons, P L De-Sá-Júnior, F Faria, I F C Batista, D M Barros-Battesti, M B Labruna, A M Chudzinski - Tavassi. Elsevier Editorial System(tm) for Biomedicine & Pharmacotherapy Manuscript Draft Manuscript Number: BIOPHA-D-11-00099 (Accept manuscript: April/2011). 7. I F Batista, O H Ramos, J S Ventura, I L Junqueira-de-Azevedo, P L Ho, A M Chudzinski-Tavassi A new Factor Xa inhibitor from Amblyomma cajennense with a unique domain composition Arch Biochem Biophys 493(2):151-156(2010). 8. A M Chudzinski-Tavassi, P L De-Sá-Júnior, S M Simons, J Ventura, I F C Batista, E Durães, E M Reis, M Demasi A new tick Kunitz type inhibitor, Amblyomin-X, induces tumor cell death by modulating genes related to the cell cycle and targeting the ubiquitin-proteasome system Toxicon 56(7):1145-1154(2010). 9. D G. L Oliveira, S M Simons, Ana M Chudzinski - Tavassi, C B Zamboni (2011) Analysis of saliva from Amblyomma cajennense (Acari: Ixodidae) species from Brazil by NAA Proceedings of 13 MTAA, 13-18 March, college Station, Texas,USA. 10. Medeiros J A G, Zamboni C B, AL Lapolli, G Kenchian, M T F da Cruz Decay of Ga 72 Appl. Radiat. Isot., 54:245-259(2001). 11. J.A.G. Medeiros, Software ATIVAÇÃO, Instituto de Pesquisas Energéticas e Nucleares, São Paulo, Brasil (2004). 12. Mei-Hwa Hsu, J R Sauer Íon and water balance in the feeding lone star tick Comp Biochem Physiol 52A:269-276(1975).

13. S F Araman, A Said, Bioxchemical and physiological studies of certains ticks (Ixodoidea). The ionic regulatory role of the coxal organs of Argas (Persicargas) persicus (Oken) and A. (P.) arboreus Kaiser, Hoogstraal and Kols (Argasidae) J. Parasit. 58: 348-353(1972). 14. Shih Chi-Yen, J R Sauer, P Eikenbary, J A Hair, J H Frick. The effects of desiccation and rehydration on the lone star tick J. Insect. Physiol. 19: 505-514(1973). 15. J Rehacek and H W Brzostowski A tick culture medium based on analyses of blood volume of insect larvae Ann ent. Soc. Am. 24, 503-507(1969). 16. J R Tatchell The ionic regulatory role of the salivary secretion of the cattle tick Boophilus microplus J. Insect. Physiol.15, 1421 1430(1969).