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. 2020 Nov 17;33:106533. doi: 10.1016/j.dib.2020.106533

Transcriptome dataset of Babesia bovis life stages within vertebrate and invertebrate hosts

Massaro W Ueti a,b,c,, Wendell C Johnson a, Lowell S Kappmeyer a, David R Herndon a, Michelle R Mousel a,c, Kathryn E Reif a,b, Naomi S Taus a,b, Olukemi O Ifeonu d, Joana C Silva d,e, Carlos E Suarez a,b, Kelly A Brayton b,c,⁎⁎
PMCID: PMC7701181  PMID: 33294524

Abstract

Babesia bovis is a hemoprotozoan parasite of cattle that has a complex life cycle within vertebrate and invertebrate hosts. In the mammalian host, B. bovis undergoes asexual reproduction while in the tick midgut, gametes are induced, fuse, and form zygotes. The zygote infects tick gut epithelial cells and transform into kinetes that are released into the hemolymph and invade other tick tissues such as the ovaries, resulting in transovarial transmission to tick offspring. To compare gene regulation between different B. bovis life stages, we collected parasites infecting bovine erythrocytes and tick hemolymph. Total RNA samples were isolated, and multiplexed libraries sequenced using paired-end 100 cycle reads of a HiSeq 2500. The data was normalized using the TMM method and analysed for significant differential expression using the generalized linear model likelihood ratio test (GLM LRT) in edgeR. To validate our datasets, ten genes were selected using NormFinder. Genes that had no significant fold change between the blood and tick stages in the RNA-Seq datasets were tested by quantitative PCR to determine their suitability as “housekeeping” genes. The normalized RNA-Seq data revealed genes upregulated during infection of the mammalian host or tick vector and six upregulated genes were validated by quantitative PCR. These datasets can help identify useful targets for controlling bovine babesiosis.

Keywords: Bovine babesiosis, Babesia, Bovine, Gene expression, Kinetes, Rhipicephalus microplus

Specifications Table

Subject Parasitology
Specific subject area Transcriptome analysis of Babesia bovis life stages.
Type of data Tables
Graphic
Excel file
How data were acquired Illumina HiSeq™ 2500
Bio-RAD CFX96™ Real-Time PCR
Data format Raw
Analysed
Parameters for data collection Babesia bovis blood stages were collected from bovines with acute parasitemia and suspended in TRIzol (Thermo Fisher Scientific, Waltham, MA). Babesia bovis kinetes were collected from infected replete female ticks by extraction via pressurized capillary tubing, pooled, concentrated, and suspended in TRIzol. Total RNA was extracted, and library construction performed according to Illumina TruSeq mRNA library protocols.
Description of data collection Counts were generated from alignments for each gene using the Subread feature of Counts v1.6.0. Genes without at least 1 read per million mapped reads across all three samples within a group were removed, data was normalized using the TMM method, and analysed for differential expression significance testing using the generalized linear model likelihood ratio test (GLM LRT) method in edgeR v3.20.9. The false discovery rate (FDR) method was employed to correct for multiple testing and genes were termed significantly differentially expressed if their logFold Change (logFC) value was greater than or equal to 1 and the FDR set to 5%.
Triplicate RNA samples from B. bovis blood or kinete stages were used for qPCR. Quantitative PCR was performed in triplicate using a Bio-RAD CFX96™ Real-Time PCR Detection System. The transcript level of six genes of interest was normalized by dividing the transcript level of the gene of interest with that of the housekeeping genes. To identify suitable “housekeeping” genes, Excel (Microsoft Office 2013) with NormFinder and the comparative delta-Ct method from the RNA-Seq dataset were used to select ten genes that had no significant fold changes between the blood and kinete stages. The top five housekeeping genes were then used to normalize transcript levels in the qPCR data.
Data source location The U.S. Department of Agriculture-ARS-Animal Disease Research Unit.
Pullman/Washington State
United States of America
46.730873 ° N, -117.163475 ° E
Data accessibility Raw data were deposited at the NCBI Gene Expression Omnibus under accession number GSE144066.
Direct URL to data: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE144066.
Related research article M.W. Ueti, W.C. Johnson, L.S. Kappmeyer, D.R. Herndon, M.R. Mousel, K.E. Reif, N.S. Taus, O.O. Ifeonu, J.C. Silva, C.E. Suarez, K.A. Brayton. Comparative analysis of gene expression between Babesia bovis blood stages and kinetes allowed by improved genome annotation. Int. J. Parasitol.
doi: 10.1016/j.ijpara.2020.08.006.

Value of the Data

  • Comparison between life stages can help identify useful targets for therapeutic intervention and vaccine development to control bovine babesiosis or block parasite infection of the tick vector.

  • These data can benefit scientists at universities, federal agencies, and international institutions working towards prevention of B. bovis.

  • These datasets may be the foundation to define potential targets for understanding transmission mechanisms of tick-borne protozoan parasites of humans and animals.

  • The kinete dataset contains reads for R. microplus hemocytes that could be used to elucidate tick responses to Babesia infection.

1. Data Description

Tables 14 show differential expression of gene families by B. bovis blood stages or kinetes, including SMORFs, SBPs, GCC2 and GCC3 domain-containing proteins, and VESAs. Normalized data were used to determined fold increase by dividing normalized counts of one stage with the other. Table 5 indicates differential gene expression associated with elements of the B. bovis glideosome between blood stages and kinetes. To validate the RNA-Seq, three test genes from either kinete stage (BBOV_I002220, BBOV_I004280, BBOV_IV011690) or blood stages (BBOV_I001680, BBOV_II002630, BBOV_III009600) were selected based on their magnitude of transcription. A panel of housekeeping genes (BBOV_IV006850, BBOV_IV009000, BBOV_III009160, BBOV_III006180, BBOV_III011560) demonstrates a consistent pattern of gene expression differences between B. bovis blood stages and kinetes. Fig. 1 illustrates the consistent ratios of housekeeping gene relative expression as compared to the test genes. Supplementary Table S1 is an Excel Spreadsheet with normalized RNA-Seq data and analyzed in the context of differential gene expression between B. bovis blood stages and kinetes. Table S1 contains B. bovis gene identifiers, Log Fold Change, Log Count per Million Reads, False Discovery Rate, triplicate reads for B. bovis blood stages and kinetes (normalized and raw counts).

Table 2.

Differential expression of the spherical body protein gene family between B. bovis blood stages and kinetes.

GeneID norm blood stages norm kinetes Fold increase in blood stages Fold increase in kinetes
BBOV_I004210 9564.525657 716.5825508 13.34741635 0.074920867
BBOV_IV005390 4059.333716 31.38524799 129.3389084 0.007731625
BBOV_II000680 3355.546841 21.10031815 159.0282581 0.006288191
BBOV_II000740 1058.592079 23.79627366 44.48562387 0.022479172
BBOV_III005860 679.0452333 5.850819611 116.0598478 0.008616244
BBOV_III005600 384.621592 4.203584114 91.49848831 0.010929142
BBOV_III006540 289.7373304 8.541515569 33.92106799 0.029480204
BBOV_III005830 252.4609668 4.173006004 60.498587 0.016529312
BBOV_III006460 239.8983689 413.0159404 0.580845303 1.721628798
BBOV_III005840 162.7218894 12.47769378 13.04102282 0.076681102
BBOV_III006520 50.57652699 0.628796749 80.43382394 0.012432581
BBOV_III005630 36.93756706 1.347535007 27.41121148 0.036481423
BBOV_III005790 19.96872969 3.655263286 5.463007211 0.183049365
BBOV_III006480 18.77035174 0.901596442 20.81901711 0.048033007
BBOV_III006500 4.383303317 0.20015859 21.89915163 0.045663869

Table 3.

Differential expression of the GCC2 and GCC3 domain containing protein gene family between B. bovis blood stages and kinetes.

GeneID norm blood stages norm kinetes Fold increase in blood stages Fold increase in kinetes
BBOV_IV006260 319.5826078 22.37882551 14.28057999 0.070025167
BBOV_III011740 197.335074 35.38007157 5.577577016 0.179289322
BBOV_IV006250 4.042298771 4387.570389 0.000921307 1085.414671
BBOV_III011730 3.208575878 2445.955909 0.001311788 762.3182379

Table 1.

Differential expression of the small open reading frame (smorf) gene family between B. bovis blood stages and kinetes.

GeneID norm blood stages norm kinetes Fold increase in blood stages Fold increase in kinetes
BBOV_III011930 2113.913468 14.36620151 147.1449127 0.006796022
BBOV_III001320 536.3841036 2.982448672 179.8468851 0.005560285
BBOV_I003880 518.6261427 7.285320965 71.18782345 0.014047346
BBOV_III007740 398.7738069 110.4001374 3.612077088 0.276849019
BBOV_II004160 380.0745053 2.545392465 149.3186259 0.006697088
BBOV_II004220 369.9142849 2.877928198 128.534925 0.007779987
BBOV_I003890 288.1595966 2.645425925 108.9274864 0.009180419
BBOV_IV007930 286.4893288 1.926687667 148.6952627 0.006725164
BBOV_II000060 280.9586624 1.984377164 141.5853133 0.007062879
BBOV_III000050 240.2349071 1.13933101 210.8561122 0.004742571
BBOV_I001120 222.2547257 36.4316058 6.10060196 0.16391825
BBOV_II006810 208.0321558 5.086740939 40.89694331 0.024451705
BBOV_IV006430 207.1816437 0.937498517 220.9941028 0.004525008
BBOV_I001180 202.7519971 1.332583402 152.1495741 0.00657248
BBOV_II002275 194.4475113 11.84410832 16.41723515 0.060911596
BBOV_IV007970 187.8401442 0.724434865 259.2919714 0.003856656
BBOV_II001390 169.3409791 10.7185897 15.79881158 0.0632959
BBOV_IV006390 126.4761588 12.76775186 9.905906709 0.100949871
BBOV_II002280 109.3296517 3.105479146 35.20540521 0.028404729
BBOV_I001370 108.4269976 0.615054735 176.2883713 0.005672524
BBOV_IV000090 99.97305676 0.97946984 102.0685402 0.009797338
BBOV_III011960 97.89184227 1.043228584 93.8354679 0.010656951
BBOV_II007780 80.91934755 0.623937094 129.6915159 0.007710605
BBOV_III000020 77.72837628 0.441915862 175.8895368 0.005685387
BBOV_IV012140 69.65059029 2.152564713 32.35702503 0.03090519
BBOV_III007710 66.79064133 32.61366171 2.047934449 0.488296879
BBOV_IV000040 66.34182859 3.766155266 17.61526647 0.05676894
BBOV_III002350 63.3051779 3.209907951 19.72180476 0.050705299
BBOV_I003860 61.03939933 1.178418838 51.79771178 0.019305872
BBOV_I001160 56.8016851 2.876162626 19.74912148 0.050635164
BBOV_III002340 51.26993531 0.410873441 124.7827924 0.008013925
BBOV_I001420 45.33252697 0.838674649 54.05257813 0.018500505
BBOV_I001170 43.73955786 0.743409174 58.83645158 0.016996266
BBOV_II007820 32.65136192 0.406850737 80.25390869 0.012460452
BBOV_II004150 31.64665067 0.486700297 65.02287115 0.015379204
BBOV_IV007960 29.20461566 0.486700297 60.00533771 0.016665184
BBOV_II002290 25.70031072 11.88324468 2.162735129 0.462377471
BBOV_II006800 16.08857604 607.0183122 0.026504268 37.72977241
BBOV_II001380 13.69017871 2.146657517 6.377439625 0.156802739
BBOV_II000400 8.75589443 406.4511482 0.021542305 46.42028881
BBOV_I005150 4.467630153 3.39732353 1.315044067 0.760430791
BBOV_I003850 3.639805192 0.281682051 12.92167951 0.077389321
BBOV_IV006420 1.559208382 4.05065043 0.384927905 2.59788908
BBOV_III000690 0.288793277 92.75983833 0.003113344 321.198053

Table 4.

Differential expression of the variant erythrocyte surface antigen (ves1) gene family between B. bovis blood stages and kinetes.

GeneID norm blood stages norm kinetes Fold increase in blood stages Fold increase in kinetes
BBOV_III000015 1.728967521 0.601312722 2.875321706 0.34778717
BBOV_III001300 1.02316527 0.401991082 2.545243701 0.392889687
BBOV_II002310 11.46011732 4.90734948 2.335296756 0.428211103
BBOV_I001190 1.921214622 0.906828737 2.118608006 0.472008034
BBOV_IV007950 1.919285603 0.94926437 2.021866261 0.494592555
BBOV_I005825 156.5772135 79.50478851 1.969406075 0.507767297
BBOV_II002320 423.6835178 220.0983315 1.924973783 0.519487594
BBOV_IV005670 331.7736784 174.558981 1.900639408 0.526138728
BBOV_II000380 41.83335358 22.80774353 1.834173272 0.545204761
BBOV_IV005660 140.5719566 82.52085286 1.703471932 0.587036382
BBOV_II000040 16.7797131 10.55649865 1.589515014 0.629122714
BBOV_III001270 24.07677147 15.19922865 1.58407851 0.631281842
BBOV_II007810 7.620384667 4.871933002 1.564139873 0.639329012
BBOV_II007830 3.44796873 2.208278049 1.561383419 0.640457679
BBOV_III001150 18.99083241 12.39033947 1.532712841 0.652437934
BBOV_I000060 3.967674309 2.651030862 1.496653383 0.668157378
BBOV_I000070 10.11356796 7.128294751 1.418792055 0.704824922
BBOV_IV002830 23.37186412 16.55999767 1.41134465 0.708544153
BBOV_III002370 12.47428832 8.974695799 1.389939959 0.719455537
BBOV_II000900 24.01138202 22.98856169 1.044492576 0.957402688
BBOV_I001410 10.98244456 12.27491138 0.894706627 1.117684803
BBOV_II000030 6.160960597 7.564935187 0.814410229 1.227882417
BBOV_III011940 26.85581707 36.03944587 0.745178413 1.341960506
BBOV_I000050 34.99932496 48.47120721 0.722064231 1.384918345
BBOV_II000945 8.125332914 12.97149013 0.626399344 1.596425681
BBOV_III007700 19.30319549 31.04248606 0.621831494 1.608152706
BBOV_II002260 0.539728944 0.905991786 0.595732712 1.678605154
BBOV_IV000030 14.53940728 24.77284468 0.586909072 1.703841443
BBOV_II006820 14.94653581 29.50277234 0.50661462 1.973886975
BBOV_III007110 420.2763021 50.88074443 8.260026594 0.121064986
BBOV_III007140 563.2564757 77.88629427 7.231779108 0.13827856
BBOV_III006920 478.708575 140.9323883 3.396725059 0.29440122
BBOV_III003060 250.1297463 78.89379732 3.170461491 0.315411495
BBOV_III006080 798.0562832 5.063209234 157.6186656 0.006344426
BBOV_IV001490 499.5313164 5.215861947 95.77157554 0.010441511
BBOV_IV007980 128.4011235 2.044485845 62.80362559 0.015922648
BBOV_III011950 53.41646004 1.155794466 46.21622756 0.021637422
BBOV_I001320 4.013872157 0.104520474 38.40273571 0.026039812
BBOV_I005865 193.6617495 5.222233452 37.08408505 0.026965746
BBOV_III002320 44.98541218 1.343047993 33.49501463 0.029855189
BBOV_I000010 32.39996069 1.048088238 30.91339021 0.032348442
BBOV_III003090 4982.64518 189.2864097 26.32331179 0.037989141
BBOV_III000090 8.739195077 0.401154131 21.78513044 0.04590287
BBOV_I005120 165.8736178 9.685269174 17.12638181 0.058389449
BBOV_I005835 90.24457916 5.64889545 15.97561505 0.062595399
BBOV_IV000350 201.2939525 17.46459112 11.52583253 0.086761628
BBOV_I001340 6.804356674 0.614217784 11.07808476 0.090268311
BBOV_IV002840 1937.126989 201.8771272 9.595574376 0.10421471
BBOV_II004130 16.85364966 2.155539876 7.818760323 0.127897513
BBOV_I005945 68.75377453 9.111370654 7.545931028 0.132521752
BBOV_I005905 96.32245181 13.5837803 7.090990116 0.14102403
BBOV_II000100 22.9740958 3.478312299 6.604954881 0.151401488
BBOV_III000700 20.52508246 3.406670199 6.024969034 0.165975957
BBOV_II001370 117.6823372 21.98983005 5.351671067 0.186857523
BBOV_I005160 58.84307326 14.5715978 4.038203227 0.247634887
BBOV_IV005640 16.05860815 5.164916596 3.109170856 0.321629157
BBOV_I005885 58.78805667 19.15570372 3.068958339 0.325843459
BBOV_III001295 2.354492652 0.778101658 3.025944783 0.330475297
BBOV_I005925 323.1792347 120.5558705 2.680742409 0.373030992
BBOV_IV000200 1221.015774 33.55945 36.38366462 0.027484862
BBOV_II004170 25.25477425 0.100497771 251.2968606 0.003979357
BBOV_III006070 971.8226855 4.00958644 242.3747935 0.004125842
BBOV_III003100 4179.375093 21.0944595 198.1266737 0.005047276
BBOV_IV001500 736.2579763 6.232070813 118.1401814 0.008464521
BBOV_I005955 156.0360625 2.111219752 73.90801565 0.013530332
BBOV_I005140 122.6569861 2.272128462 53.98329723 0.018524248
BBOV_IV007990 399.8551031 8.592072955 46.5376755 0.021487966
BBOV_II000370 203.6019731 4.45954771 45.65529653 0.021903264
BBOV_III002330 82.99101801 2.13898475 38.79925651 0.02577369
BBOV_III002310 47.30825938 1.381833563 34.23585926 0.02920914
BBOV_I005935 204.0221091 6.004055555 33.98071641 0.029428455
BBOV_III007690 56.20382698 1.679979071 33.45507569 0.029890831
BBOV_II004190 31.41995041 1.005279965 31.25492549 0.031994957
BBOV_I005895 36.94778066 1.235341766 29.90895449 0.033434803
BBOV_I005915 69.19411686 2.391600542 28.93213798 0.03456364
BBOV_III000040 22.04538552 0.841860402 26.18650963 0.038187602
BBOV_I005845 85.75392604 3.346863777 25.622174 0.039028694
BBOV_III000710 24.83032387 0.978632889 25.37246004 0.039412812
BBOV_II004120 62.60907076 2.697046176 23.21394098 0.043077563
BBOV_III007730 100.4983749 4.340448271 23.15391604 0.043189238
BBOV_III007720 52.02941561 2.278964278 22.83029011 0.043801458
BBOV_IV006410 37.49204361 1.667538318 22.48346752 0.044477125
BBOV_I005875 56.76625474 3.27019997 17.3586494 0.057608169
BBOV_II001400 133.9557957 7.782021543 17.21349587 0.058093952
BBOV_I005815 72.0948074 4.198351819 17.17216911 0.058233761
BBOV_IV006400 39.62063076 2.351978021 16.84566369 0.059362458
BBOV_IV000060 20.97555289 1.258803089 16.66309295 0.060012868
BBOV_IV007910 38.04169291 2.348792269 16.19627815 0.06174258
BBOV_I003870 19.33495425 1.212344753 15.94839604 0.06270223
BBOV_I001330 9.327555329 0.692555493 13.46831471 0.074248339
BBOV_II002270 9.706371156 0.770428891 12.59865936 0.079373525
BBOV_III000100 25.84479748 2.285406166 11.30862333 0.088428093
BBOV_I000020 110.8671163 9.939986566 11.1536485 0.089656761
BBOV_II001410 55.15815454 6.181125463 8.923642607 0.112061861
BBOV_IV005680 278.7178629 33.63615638 8.286257791 0.120681739
BBOV_I004520 17.03969061 2.704022755 6.301607696 0.158689663
BBOV_II006780 54.01289193 8.834899055 6.113583369 0.163570191
BBOV_IV002850 2371.499271 427.4573271 5.547920507 0.180247716
BBOV_I001140 10.81090535 2.000911002 5.402991609 0.185082649
BBOV_II002300 2.672564091 0.513720014 5.202374875 0.192219904
BBOV_IV007920 25.37602988 5.163242694 4.914746679 0.203469286
BBOV_II000940 125.7918935 25.9247027 4.852201968 0.206091998
BBOV_I005180 101.9253517 21.35619549 4.772636203 0.209527808
BBOV_I003840 9.184526328 2.050646761 4.478843701 0.223271913
BBOV_II004140 15.36332175 3.952571843 3.886917773 0.257273258
BBOV_I001430 17.06123265 4.433667203 3.848108545 0.259867929
BBOV_II006830 23.9118131 6.226676466 3.8402209 0.260401687
BBOV_I003830 5.60933158 1.611452341 3.480916832 0.287280636
BBOV_II000920 35.70692278 11.62363102 3.071925004 0.32552878
BBOV_I003900 16.74032752 6.142248224 2.72543976 0.366913265
BBOV_I001440 6.681265191 2.610360801 2.559517898 0.390698577
BBOV_II000110 24.00063777 9.819882162 2.444086128 0.409150884
BBOV_II000390 11.18485422 4.944482435 2.262087966 0.442069457
BBOV_IV002860 18.92967276 37.88463844 0.499666185 2.001336153
BBOV_III003110 89.20183852 188.362042 0.473565892 2.111638562
BBOV_III001220 1.72155826 4.18135367 0.411722709 2.42881915
BBOV_I003910 10.52155624 26.5396865 0.396446139 2.522410743
BBOV_IV001510 2.698503508 7.92944196 0.340314428 2.938459015
BBOV_II000910 25.91710922 93.57840916 0.276956078 3.610680819
BBOV_I005805 8.085385626 43.16715254 0.187304122 5.338910788
BBOV_II006790 28.98624709 163.5550893 0.177226201 5.642506559
BBOV_I000030 45.94475751 345.461503 0.132995304 7.519062496
BBOV_III001280 55.72201753 624.213682 0.089267536 11.20228071
BBOV_I005110 5.925071676 74.15213411 0.079904264 12.51497672
BBOV_IV006380 8.428348062 113.9017072 0.073996679 13.51412001
BBOV_III001160 42.67923143 686.2582539 0.06219121 16.07944264
BBOV_I004510 17.47781955 597.9515367 0.029229492 34.21202141
BBOV_I005190 9.67496017 562.8547934 0.017189087 58.17644554
BBOV_III000670 4.364457017 969.2748263 0.004502807 222.0837146

Table 5.

Differential gene expression of glideosome elements between B. bovis blood stages and kinetes

GeneID norm blood stages norm kinetes Fold increase in blood stages Fold increase in kinetes
BBOV_II006100 5.338814 70978.19 7.52177E-05 13294.74914
BBOV_II006070 1.414999 4259.571 0.000332193 3010.298479
BBOV_II002650 96.21683 164058.8 0.000586478 1705.095019
BBOV_II006080 8.861071 13495.36 0.000656601 1522.994638
BBOV_IV003210 352.6652 26835.99 0.013141504 76.09479332
BBOV_IV008510 325.7201 6390.77 0.050967269 19.62043538
BBOV_IV009790 93.05779 1545.97 0.060193791 16.61300904
BBOV_I000300 1768.456 22238.81 0.079521131 12.57527387
BBOV_II004420 118.6838 1229.741 0.096511253 10.36148606
BBOV_I003490 637.5578 6256.353 0.101905671 9.812996615
BBOV_II006000 509.7894 3351.442 0.152110493 6.574168436
BBOV_II005470 286.0339 670.0373 0.426892467 2.342510298
BBOV_II005940 32.09359 0.249803 128.4757525 0.00778357
BBOV_IV011430 584.8345 5.444342 107.4206191 0.0093092
BBOV_IV011230 537.6968 24.69678 21.77194044 0.045930679
BBOV_II003100 132.8903 6.408557 20.73637991 0.048224425
BBOV_I001630 500.6437 28.21142 17.7461369 0.056350292
BBOV_II005930 150.9749 10.4024 14.51346609 0.068901529
BBOV_II002890 679.6739 61.55152 11.04235702 0.090560376
BBOV_II002630 824.4089 197.8921 4.165952089 0.240041167

Fig. 1.

Fig 1

Ratios of housekeeping gene relative expression as compared to the test genes. The top panel are genes upregulated in B. bovis blood stages and the bottom panel are genes upregulated in kinetes.

2. Experimental Design, Materials and Methods

Three splenectomized Holstein calves approximately four months of age and determined to be Babesia-free by competitive enzyme-linked immunosorbent assay and PCR [1,2,3] were used for acquisition of B. bovis Texas strain by R. microplus, La Minita strain, as previously described [1,4]. Approximately 40,000 R. microplus larvae were placed under a cloth patch on calves. When ∼1% of the ticks had molted to the adult stage, calves were intravenously inoculated with B. bovis stabilate containing 107 infected erythrocytes to synchronize female tick repletion with an ascending parasitemia. Replete female ticks were collected and incubated at 26 °C in 96% relative humidity to allow B. bovis development [1,2].

To increase the percent parasitized erythrocytes, blood samples from an acute parasitemia were cultured for 5 days at 3% oxygen and 5% carbon dioxide [5,6]. These in vitro cultured B. bovis blood stages were centrifuged, media removed, cells suspended in TRIzol (Thermo Fisher Scientific, Waltham, MA) and stored at -80 °C. Babesia bovis kinetes were collected from replete female ticks by extraction using pressurized capillary tubing, pooled, concentrated by centrifugation at 3,000 × g for 2 min, suspended in TRIzol and stored at -80 °C. To isolate RNA, the samples were thawed, transferred into Lysing Matrix H tubes and homogenized three times for 30 s at a speed setting of 6.0 m/s (MP Biomedicals, Solon, OH) with cooling of samples on ice for 5 min between runs. Homogenized samples were transferred into microfuge tubes and centrifuged for 1 min at 16,000 x g at 4 °C to remove large particulates. Sample supernatants were transferred to microfuge tubes to which 200 µl of chloroform per ml of TRIzol supernatant was added. The samples were vortexed for 15 s and incubated at room temperature for 3 min. For phase separation, samples were centrifuged at 16,000 x g for 15 min at 4 °C and the upper aqueous phase transferred to a new microfuge tube. Subsequent RNA isolation was accomplished using the RNA Cleanup and Concentrator kit (Zymo Research, Irvine, CA) according to the manufacturer's instructions. In brief, two volumes of RNA binding buffer were added to the aqueous phase, mixed, an equal volume of 100% ethanol added, and mixed again. A volume of 800 µl of each sample was transferred to RNA-25 concentrator column assemblies and the RNA bound to the column matrix by passing the sample through the column by centrifuging at 13,000 x g for 30 s. To the sample-bound column, 400 µl of RNA prep buffer was added and spun at 13,000 x g for 30 s. Samples were washed by adding 800 µl of RNA wash buffer to each column, centrifuged at 13,000 x g for 30 s, washed again with 400 µl of RNA wash buffer, and centrifuged for 2 min at 13,000 x g after the final wash. Columns were transferred to new 1.5 ml tubes and samples eluted by adding 60 µl of nuclease-free water. Samples were treated with TURBO DNase (ThermoFisher Scientific) according to the manufacturer's instructions. Reactions were terminated and samples concentrated using RNA Cleanup and Concentrator RNA-5 or RNA-25 columns as described above. Sample RNA concentrations were determined using a NanoDrop 1000 (ThermoFisher Scientific) and tested for residual DNA by Real-Time SYBR Green PCR targeting of BBOV_II006950. If DNA contamination was observed, samples were re-treated with TURBO DNase as described above until samples were confirmed to be free of DNA. RNA samples were stored at -80 °C. Total RNA was monitored for quality control using the Agilent Bioanalyzer Nano RNA chip (Agilent Technologies, Santa Clara, CA) and NanoDrop absorbance ratios for 260/280nm and 260/230nm. Library construction was performed according to the Illumina TruSeq mRNA (Illumina, San Diego, CA) stranded protocol. Using an input quantity for total RNA within the recommended range, mRNA was enriched using oligo dT magnetic beads. The enriched mRNA was chemically fragmented. First strand synthesis used random primers and reverse transcriptase to make cDNA. After second strand synthesis the ds cDNA was cleaned using AMPure XP beads (Beckman Coulter, Brea, CA) and the cDNA was end repaired and the 3’ ends adenylated. Illumina barcoded adapters were ligated to the ends and the adapter ligated fragments were enriched by nine cycles of PCR. The resulting libraries were validated by qPCR and sized using an Agilent Bioanalyzer DNA high sensitivity chip. The library concentrations were normalized and then multiplexed. The multiplexed libraries were sequenced using paired end 100 cycle chemistry for the HiSeq 2500 (Illumina). The version of HiSeq control software was HCS 2.2.58 with real time analysis software, RTA 1.18.64. Low quality reads were filtered before alignment to the new reference genome using STAR v2.5.2a (2-pass mapping). Counts were generated from alignments for each gene using the Subread feature of Counts v1.6.0. Genes without at least 1 read per million mapped reads across all three samples within a group were removed, data were normalized using the TMM method, and analysed for differential expression significance testing using the generalized linear model likelihood ratio test (GLM LRT) method in edgeR v3.20.9. The false discovery rate (FDR) method was employed to correct for multiple testing and genes were termed differentially expressed if their log Fold Change (logFC) value was greater than or equal to 1 with the FDR set to 5%. Triplicate RNA samples from B. bovis blood or kinete stages were used for qPCR. Approximately 100 ng of total RNA from each preparation of parasites was reverse transcribed using a Superscript III™ cDNA Synthesis Kit (ThermoFisher Scientific) following the manufacturer's protocol. Quantitative PCR was performed in triplicate using a Bio-RAD CFX96™ Real-Time PCR Detection System. Reaction volumes were 20 μl using 10 μl SsoFast™ EvaGreen® Supermix (Bio-Rad, Hercules, CA, USA), 1 μl of 500 nM of each primer set, 6 μl of nuclease-free water and 2 μl of a 1:10 dilution of cDNA as template. The conditions consisted of an enzyme activation step of 98 °C for 2 min followed by 40 cycles of 98 °C for 5 s and 55 °C for 5 s. The transcript level of six genes of interest was normalized by dividing the transcript level of the gene of interest with that of the housekeeping genes. To identify suitable “housekeeping” genes, Excel (Microsoft Office 2013) with NormFinder and the comparative delta-Ct method from the RNA-Seq dataset were used to select five genes that had no significant fold changes between the blood and kinete stages [7]. The selected housekeeping genes were then used to normalize transcript levels in the qPCR data.

3. Ethics Statement

Animal experiments were conducted with the approval of the Institutional Animal Care and Use Committee of the University of Idaho, Moscow, Idaho, in accordance with institutional guidelines based on the U.S. National Institutes of Health Guide for the Care and Use of Laboratory Animals. Splenectomies were performed under sedation with xylazine and isoflurane inhalation, and all efforts were made to minimize suffering. All animals exposed to an exotic pathogen and ticks were euthanized. These animals were sedated with xylazine, brought to a recumbent position and euthanized by intravenous injection of sodium pentobarbitone. IACUC #2018-16.

CRediT Author Statement

Massaro Ueti, Wendell Johnson, and Kelly Brayton: Conceptualization. Massaro Ueti, Wendell Johnson, Lowell Kappmeyer, David Herndon, Kathryn Reif: Methodology. Massaro Ueti, Wendell Johnson, Lowell Kappmeyer, David Herndon, Michelle Mousel, Carlos Suarez and Kelly Brayton: Data curation, Writing-Original draft preparation. Massaro Ueti, Wendell Johnson, and Kelly Brayton: Visualization, Investigation. Massaro Ueti: Supervision. Massaro Ueti, Wendell Johnson and Kelly Brayton: Validation of data. Massaro Ueti, Wendell Johnson, Naomi Taus, Olukemi Ifeonu, Joana Silva, Carlos Suarez, and Kelly Brayton: Writing- Reviewing and Editing.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships which have, or could be perceived to have, influenced the work reported in this article.

Acknowledgments

We would like to thank Nicholas Durfee, Paul Lacy, and Jacob Laughery for their laboratory support and Ralph Horn, Kathy Mason, James Allison, and Megan Jacks for their excellent assistance with animal care. This work was supported by the United States Department of Agriculture-Agricultural Research Service (Project # 2090-32000-039-00D), U.S. Agency for International Development (Grant # AID-BFS-P-13-00002) and National Institute of Food and Agriculture-Agriculture and Food Research Initiative Competitive Grant (Project # 2016-67015-24968 to MWU).

Footnotes

Supplementary material associated with this article can be found in the online version at doi:10.1016/j.dib.2020.106533.

Contributor Information

Massaro W. Ueti, Email: massaro.ueti@usda.gov.

Kelly A. Brayton, Email: kbrayton@wsu.edu.

Appendix. Supplementary materials

mmc1.xlsx (1.2MB, xlsx)

References

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

mmc1.xlsx (1.2MB, xlsx)

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