RNA-dependent control of gene expression is crucial for bacterial adaptation to environmental stresses, such as fluctuations in ambient temperature. In the enteric pathogen Salmonella Typhimurium, a drastic downshift in temperature immediately triggers the “cold shock response” in which selective expression of cold shock proteins (CSPs) aids acclimatisation. The major cold shock protein, CspA, and some of its homologues function as RNA chaperones and play critical roles in destabilising aberrant RNA secondary structures that form at reduced temperatures. However, the precise roles and targets of this protein family remain unclear. With the aim of generating a genome-wide map of protein-RNA interactions, in vivo UV cross-linking and analysis of cDNA (CRAC) was performed. This novel, high-throughput technique allows identification of all RNA targets for a particular protein, which in this case was the cold-induced protein CspA, and constitutively expressed CspE. CRAC results reveal a remarkable number and diversity in the RNA targets of these CSPs. For example, CspA targets approximately 25% of the RNA encoded by the Salmonella genome. CspA and CspE were shown to target mRNAs encoding proteins involved in metabolism, stress, cell division and RNA turnover, as well as a number of mRNAs that are cold shock-inducible. Bioinformatic analyses have shown that mainly protein coding regions are targeted and, interestingly, 5’ untranslated regions (UTR) and small RNAs, which often play roles as regulators of translational control. There also appears to be a reproducible pattern of repeated binding along mRNA transcripts, suggesting a role for these Csps in maintaining mRNAs in a linear conformation, which is required for efficient translation. To validate targets, phenotypic analyses were performed, including growth studies during amino acid starvation, and the response to heat shock and UV DNA damage. These experiments confirmed involvement of the paralogues, and further bioinformatic analysis revealed that these proteins were targeting key regulatory regions on some specific targets. A more in-depth analysis was carried out on one target – the general stress response sigma factor RpoS (σS) and a model of CspA paralogue involvement in regulating the mRNA of this target is presented. Overall, the in vivo data from this study suggests that these cold shock proteins are crucial for modulating key cellular processes beyond that which their name implies.

Salmonella enterica sv. typhimurium is a major food-borne pathogen, in part because of its ability to persist and multiply at low temperatures. Adaptation to refrigerated temperatures involves induction of a multigenic cold shock response (CSR); where gene expression is co-ordinately modified, to express cold shock proteins (CSPs). Characterisation of CspA, the major cold shock protein, instigated the identification of other CspA paralogues; which are highly conserved and widespread across species. Six CspA paralogues have previously been identified in S. typhimurium and a csp null strain, lacking all CspA paralogues made. This strain is unable to grow following cold shock, demonstrating that the CspA paralogues play an essential role during low temperature adaptation. The individual CspA paralogues exhibit distinct expression profiles; including expression of CspC and CspE at optimal temperature and CspA and CspB following cold shock. This work investigates the transcriptional changes of S. typhimurium during cold shock and the role of the CspA paralogues under both optimal and cold shock conditions. Using a bacteriophage Mu transposon library (Francis and Gallagher, 1993) this study identifies 7 novel cold induced targets and analyses their native expression levels in SL1344 and the csp null strain during cold shock. This revealed that the regulation of 5 discrete loci including tRNApro2, cpxP and 3 uncharacterised ORFS are mediated by CspA paralogues. In addition, the transcriptional profiles of a highly conserved and essential set of genes encoding known cold shock proteins, NusA, IF2, RbfA, PNPase and CsdA have been characterised. Comparative Northern analysis of SL1344 and the csp null strain has identified a role for CspA paralogues in mediating low temperature induction of three of these genes, through transcription anti-termination. Taken together these results demonstrate that during adaptation to low temperature CspA paralogues regulate expression of genes involved in the translational machinery and metabolic biosynthetic pathways: possibly through a number of transcriptional and post transcriptional processing events. Furthermore this study provides in vivo evidence of the RNA binding activity of the S. typhimurium CspA paralogues. Using fusion proteins, the RNA targets of CspE at 37°C and CspA at 10°C were isolated and analysed. This work identifies 17 direct binding targets for CspE and these indicate that CspE performs a role at optimal growth temperature in regulating components of metabolic (coaA and plsX), translational (EF-Tu, EF-G and IF3) and virulence associated (hha) pathways. Functional redundancy between CspE and CspA was suggested as both paralogues bound 16s rRNA. In light of these findings, the functions of CspA & CspE at optimal and low temperature are discussed. Overall this study has revealed novel information about low temperature adaptation of S. typhimurium, expanding our knowledge of the complexity and importance of the CSR in bacterial pathogens. In addition this work enhances our comprehension of the roles of the CspA paralogues at both optimal and low temperature.

In cold temperatures, the survival of Salmonella enterica serovar Typhimurium (S. Typhimurium) requires the action of cold shock protein A (CspA) paralogues. These are thought to melt misfolded ribonucleic acids, facilitating their translation at low temperatures. However, through phenotypic analysis of our SL1344 csp null mutant (lacking all CspA paralogues), it has been shown that CspA paralogues function during other environmental stresses, outwith temperature reduction, and play an essential role in colony formation of an SL1344 rpoS mutant at 37°C. The general stress σ subunit, RpoS, plays an important role in adapting cells to a number of stresses including oxidative stress, temperature changes, low pH and stationary phase. Under such conditions, RpoS acts as an ‘emergency co-ordinator’, subsequently inducing the transcription of necessary stress response genes. In Escherichia coli, RpoS is regulated posttranscriptionally by at least three small RNAs (sRNAs): OxyS, DsrA and RprA; that require interactions with the Sm-like RNA chaperone, Hfq. In S. Typhimurium, the stability of the RpoS protein itself is regulated by ClpXP, an ATP-dependent protease responsible for RpoS degradation, and a specific recognition factor that targets RpoS to this protease, MviA. The present study has shown that the CspA paralogues of S. Typhimurium are involved in the expression of RpoS and aims to elucidate the role of these proteins in RpoS production. Comparative phenotypic tests were carried out in strains carrying mutations in rpoS, hfq and the csp genes to gain insight into the interactions of Hfq and CspA paralogues, with respect to RpoS expression. Both significant phenotypic overlaps, such as peroxide sensitivity, and phenotypes unique to certain mutant strains, such as cold acclimation in the csp null strain, were observed. CspA paralogues and Hfq are functionally distinct, not only in their involvement in RpoS expression, but also in RpoS-independent processes, such as cold acclimation, motility and to some extent, growth at 37°C. The roles of Hfq and the CspA paralogues, in RpoS expression, were also assessed at the molecular level. A combination of qRT-PCR analysis, transcriptional fusions and immunoblotting (with anti-σ antibodies) has shown that DsrA and RprA are not essential for RpoS expression in S. Typhimurium, during stationary phase or exponential cold shock, and do not require Hfq under these conditions. Contrary to reports in E. coli, DsrA is not induced upon cold shock in SL1344. Northern blots have shown that neither Hfq nor the CspA paralogues are involved in regulating rpoS transcription during either stationary phase at 37°C or cold shock in exponential phase. Immunoblotting and translational fusions have identified different pathways for the regulation of RpoS during stationary phase at 37°C and cold shock in exponential phase. Hfq is involved during the former condition only, whilst CspA paralogues are involved in both. Protein stability experiments have shown that the CspA paralogues do not play a major role in stabilising RpoS protein against degradation. Together, these results have pointed to a role for both the CspA paralogues and Hfq in facilitating the efficient translation of rpoS mRNA. An SL1344 csp null rpoS mutant is unable to form colonies on LB agar at 37°C, a phenomenon found when introducing combinations of mutations to SL1344 for phenotypic assessment. A conditional rpoS mutant revealed that the SL1344 csp null rpoS strain is viable but non-culturable. From the csp gene family, only cspA and cspB were able to restore colony forming ability to the rpoS mutant. Further complementation experiments pointed to faulty cell division, due to abnormal RNase E activity, as the cause.

Upon encountering stress conditions, cells must rapidly alter their gene expression and re-model their RNA complement to deal with the changing environment. As a consequence, both new RNA transcription as well as RNA degradation must take place. Accordingly, the RNA degradative machinery may adjust to the changes in RNA metabolism. Thus, a study of the response of the three major degradative exoribonucleases in Escherichia coli, polynucleotide phosphorylase, RNase II, and RNase R, to stress is of significant importance. RNase R, a processive 3' to 5' exoribonuclease, is unique among the known E. coli exoribonucleases in its ability to digest through RNAs containing extensive secondary structure without the aid of a helicase. In vivo, RNase R plays important roles in quality control of stable RNA, decay of mRNA with extensive repetitive extragenic palindromic (REP) sequences, cell-cycle regulated degradation of tmRNA in Caulobacter crescentus, as well as processing of rRNA under low temperature in P. syringae. In this dissertation, RNase R was shown to be unusual among the E. coli exoribonucleases in its dramatic response to a variety of stress conditions. Elevation of RNase R activity by as much as 10-fold was observed in response to entry into stationary phase, starvation and cold shock, and an ~3-fold increase was seen during growth in minimal medium compared to rich medium. The elevation in RNase R activity was associated with an increase in RNase R protein. Phenotypes of rnr mutants were also investigated, and RNase R was found to contribute to cell growth and viability. Further investigation of the regulation of RNase R during stress, primarily in stationary phase, revealed a novel regulation mechanism. Despite the large increase in RNase R protein and activity in stationary phase, rnr message actually decreased to only ~14% of its level in exponential phase. Further study revealed that RNase R is highly unstable in exponential phase and becomes stabilized during stationary phase, cold shock, and in minimal medium. Investigation of proteolysis on the unusual instability of RNase R indicated that both Lon and ClpXP play a role. In the absence of Lon, RNase R stability is increased ~10-fold. Based on these results, I propose that the increase in RNase R during stress is due to its enhanced stability under those conditions.

Despite their name, a number of the cold shock proteins are expressed during normal growth, and not just during cold shock, in several species. The function of these constitutively expressed CspA paralogues is unclear. In Salmonella Typhimurium (a major worldwide cause of gastrointestinal disease) they have been linked to various stress responses and the establishment of virulence. Study of the cold shock proteins as gene regulators is therefore of great interest, and they also have potential as targets for antimicrobial development. CspE in Salmonella Typhimurium is constitutively expressed during normal growth. In order to determine its function, attempts were made to identify the interactions it forms with other cellular proteins. Initially, a proteomic investigation attempted to identify proteins which complex with CspE by in vivo cross-linking and affinity purification followed by mass spectrometry. Although no defined complex was consistently identified, the results suggested a handful of proteins which might interact with CspE in a weak or transient manner. These proteins included many from the nucleoid and ribosomal entry site, hinting at CspE’s cellular localisation. In order to investigate these transient interactions, a bacterial two-hybrid system was employed. Interactions between CspE and HupA, a nucleoid protein identified in the proteomic analysis, were probed, as were interactions between CspE and CsdA, an RNA helicase thought to function co-operatively with CspE. The twohybrid system also allowed investigation of CspE dimerisation, which has been reported in vitro but not investigated in vivo until this study. CspE appears not to interact significantly with either HupA, CsdA, or itself at 37oC. Finally in a further attempt to identify interactions of CspE, a genomic library was created to test CspE interactions by two-hybrid assay with random peptides derived from the whole Salmonella genome. The library was successfully created and screened for evidence of interaction, and revealed an association between CspE and a transcriptional repressor, DeoT. DeoT is a repressor of several genes for catabolic processes, suggesting a role for CspE in the regulation of central metabolism. The findings of this work present a number of novel discoveries and several interesting opportunities for further studies.

Com objetivo de elucidar se CspD em Caulobacter crescentus possui a mesma função que em E. coli de inibir a replicação do DNA, foi avaliado o efeito da superexpressão de CspD em C. crescentus, e constatamos que, diferentemente do observado em E. coli, não houve efeito deletério ao crescimento. Quando superexpressa em E. coli, CspD de C. crescentus não demonstrou efeito no crescimento da bactéria. Além disso, através da eletroforese bidimensional do mutante deletado de cspD, foi investigado se a proteína afeta o padrão de expressão de outras proteínas. Além da protease ClpP, enzimas envolvidas no metabolismo de purinas e aminoácidos estão entre as que demonstraram expressão diferencial na ausência do gene cspD. Os dados obtidos na eletroforese bidimensional foram validados por meio de qRT-PCR. Um ensaio da ligação de CspD com ácidos nucléicos foi realizado mas, não se observou ligação entre a proteína e o DNA ou RNA. Finalmente, foi possível concluir, por meio de ensaios de western blotting, que CspD sofre regulação pós traducional pela protease Lon. / In order to elucidate if CspD in Caulobacter crescentus has the same role as in E. coli, we analyzed the effect of overexpressing CspD in bacterial growth and concluded that opposite from what its observed in Escherichia coli, it didnt affect growth. Yet, when over expressed in E. coli, CspD did not show any effect on the bacterial growth. Through two-dimensional gel electrophoresis of the cspD null mutant, it was possible to investigate if the protein is affecting the expression pattern of the cell. Along with ClpP protease, enzymes that are involved in the purine and amino acid metabolism are among those that showed differential expression in the absence of cspD. The data obtained from the two-dimensional gel electrophoresis were validated through qRT-PCR. The binding of CspD to nucleic acids was investigated. However, no binding of the protein to the nucleic acids was observed. Finally through western blotting assays, it was possible to conclude that CspD is post- translationally regulated by the Lon protease.

O uso de protocolos de diluição bitérmica está aumentando em centros de inseminação artificial e é necessário garantir que as doses de inseminação tenham a mesma qualidade quando comparado com protocolos de diluição isotérmica. Quatro ejaculados de cada 19 reprodutores PIC® foram coletados e distribuídos em split sample em três tratamentos: diluição bitérmica em duas etapas (T1), diluição isotérmica em duas etapas (T2) e diluição isotérmica em uma etapa (T3). A curva de temperatura para os três tratamentos foi feita utilizando um data logger com sensor de temperatura. As doses inseminantes foram preparadas utilizando o diluente BTS e armazenadas a 16ºC e usadas para avaliação dos parâmetros espermáticos através do Sistema CASA e avaliação de morfologia espermática, durante 120 horas. A temperatura das amostras de sêmen submetidas à diluição bitérmica em duas etapas alcançou 24,1ºC durante 120 minutos , enquanto que as amostras submetidas à diluição isotérmica em uma ou duas etapas alcançou 26,8ºC e 27,0ºC, respectivamente. A motilidade total, a progressiva e BCF foram influenciadas (P<0,05) pelo tempo de diluição, mas não pelo protocolo de diluição. A motilidade total e progressiva diminuiu com o tempo de armazenamento (91.0 ± 0.91 para 81.5 ± 1.08 % e 74.0 ± 2.48 para 60.4 ± 2.59% de 24h para 120h, para MOT e PROG, respectivamente) enquanto BCF diferiu entre 24 e 120h (28.6 ± 0.76 e 27.3 ± 0.79 Hz). As seguintes características de motilidade não foram afetadas pelo protocolo de diluição e pelo tempo de armazenamento: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB e ALH. Às 72 h de armazenamento, a morfologia espermática não diferiu entre os tratamentos (P>0.05), apresentando uma média geral de 9.2 ± 0.36 defeitos totais. Concluindo, a diluição bitérmica torna o processo de produção de doses inseminantes mais rápido, pois demoraram menos tempo para alcançar a temperatura próxima de armazenamento, sem comprometer a qualidade das doses inseminantes produzidas. / The use of bithermic dilution protocols is increasing in artificial insemination centers, being necessary to guarantee that the quality of insemination doses remain the same when compared to isothermic dilution protocols. Four ejaculates from each one of 19 crossbreed PIC® boars were collected and assigned, in a split sample design, in to three treatments: two step bithermic dilution (T1), two step isothermic dilution (T2) and one step isothermic dilution (T3). Temperature curve for the three treatments was recorded using a temperature sensor data logger. Semen doses prepared with BTS extender were stored at 16°C and were used to evaluate sperm parameters through CASA system and sperm morphology, during 120 h. The temperature in semen samples submitted to a two-step bithermic dilution reached 24.1ºC during 120 min, whereas one or two-step isothermic dilution samples reached 26.8ºC and 27.0ºC, respectively. Total motility, progressive motility and BCF were influenced (P<0.05) by the storage time but not by the dilution procedure. Total and progressive motility reduced throughout the storage time (91.0 ± 0.91 to 81.5 ± 1.08 % and 74.0 ± 2.48 to 60.4 ± 2.59% from 24h to 120h, for MOT and PROG respectively) whereas BCF differed between 24 and 120h (28.6 ± 0.76 and 27.3 ± 0.79 Hz). The following motility traits were neither affected by the dilution procedure nor by the time of storage: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB, and ALH. At 72 h of storage, sperm morphology was not different among treatments (P>0.05), showing an overall mean of 9.2 ± 0.36 total defects. In conclusion, the bithermic dilution makes the process of artificial insemination doses production faster by taking less time to reach a temperature close to that of storage, without impairing semen quality.

Upon exposure to heat or cold, Arabidopsis thaliana seedlings undergo rapid transcriptional reprogramming of several hundreds of genes that promote stress tolerance. Despite extensive characterisation of the transcriptional responses to these stimuli, however, relatively little is known about the mechanisms by which temperature signals are perceived and transduced in plant cells. High or low seasonal temperatures have large impacts on crop productivity and are expected to intensify given current global climatic projections. It is therefore of agricultural importance to better understand temperature signalling pathways in plants in order to find solutions to this problem. In this thesis, a chemical genomics screen for molecules activating or repressing heat-inducible genes in A. thaliana was performed in collaboration with Syngenta and the biological targets of these chemicals were predicted based on structural similarities to compounds with known modes of action. Many molecules that affect the function of chloroplasts or mitochondria either activate or repress heat-responsive genes, thus implicating these organelles in the regulation of plant temperature responses. In addition, the translation inhibitor cycloheximide was identified as a repressor of heat-inducible genes and an activator of early cold-inducible genes. Diverse translation inhibitors trigger a cytosolic influx of calcium ions and several inhibitors of translation elongation were found to strongly activate cold-inducible gene expression in a calcium-dependent manner. Furthermore, it was demonstrated that cold shock causes rapid translation repression in A. thaliana seedlings and that the elongation factor LOS1 is involved in cold- or cycloheximide-induced gene expression, thus implicating translational machinery in the regulation of temperature signalling in plants. Finally, one of the chemicals identified in the screen, S01A463859Y, was found to improve heat resilience in A. thaliana and may therefore be of potential use in enhancing crop productivity during thermal stress.

O uso de protocolos de diluição bitérmica está aumentando em centros de inseminação artificial e é necessário garantir que as doses de inseminação tenham a mesma qualidade quando comparado com protocolos de diluição isotérmica. Quatro ejaculados de cada 19 reprodutores PIC® foram coletados e distribuídos em split sample em três tratamentos: diluição bitérmica em duas etapas (T1), diluição isotérmica em duas etapas (T2) e diluição isotérmica em uma etapa (T3). A curva de temperatura para os três tratamentos foi feita utilizando um data logger com sensor de temperatura. As doses inseminantes foram preparadas utilizando o diluente BTS e armazenadas a 16ºC e usadas para avaliação dos parâmetros espermáticos através do Sistema CASA e avaliação de morfologia espermática, durante 120 horas. A temperatura das amostras de sêmen submetidas à diluição bitérmica em duas etapas alcançou 24,1ºC durante 120 minutos , enquanto que as amostras submetidas à diluição isotérmica em uma ou duas etapas alcançou 26,8ºC e 27,0ºC, respectivamente. A motilidade total, a progressiva e BCF foram influenciadas (P<0,05) pelo tempo de diluição, mas não pelo protocolo de diluição. A motilidade total e progressiva diminuiu com o tempo de armazenamento (91.0 ± 0.91 para 81.5 ± 1.08 % e 74.0 ± 2.48 para 60.4 ± 2.59% de 24h para 120h, para MOT e PROG, respectivamente) enquanto BCF diferiu entre 24 e 120h (28.6 ± 0.76 e 27.3 ± 0.79 Hz). As seguintes características de motilidade não foram afetadas pelo protocolo de diluição e pelo tempo de armazenamento: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB e ALH. Às 72 h de armazenamento, a morfologia espermática não diferiu entre os tratamentos (P>0.05), apresentando uma média geral de 9.2 ± 0.36 defeitos totais. Concluindo, a diluição bitérmica torna o processo de produção de doses inseminantes mais rápido, pois demoraram menos tempo para alcançar a temperatura próxima de armazenamento, sem comprometer a qualidade das doses inseminantes produzidas. / The use of bithermic dilution protocols is increasing in artificial insemination centers, being necessary to guarantee that the quality of insemination doses remain the same when compared to isothermic dilution protocols. Four ejaculates from each one of 19 crossbreed PIC® boars were collected and assigned, in a split sample design, in to three treatments: two step bithermic dilution (T1), two step isothermic dilution (T2) and one step isothermic dilution (T3). Temperature curve for the three treatments was recorded using a temperature sensor data logger. Semen doses prepared with BTS extender were stored at 16°C and were used to evaluate sperm parameters through CASA system and sperm morphology, during 120 h. The temperature in semen samples submitted to a two-step bithermic dilution reached 24.1ºC during 120 min, whereas one or two-step isothermic dilution samples reached 26.8ºC and 27.0ºC, respectively. Total motility, progressive motility and BCF were influenced (P<0.05) by the storage time but not by the dilution procedure. Total and progressive motility reduced throughout the storage time (91.0 ± 0.91 to 81.5 ± 1.08 % and 74.0 ± 2.48 to 60.4 ± 2.59% from 24h to 120h, for MOT and PROG respectively) whereas BCF differed between 24 and 120h (28.6 ± 0.76 and 27.3 ± 0.79 Hz). The following motility traits were neither affected by the dilution procedure nor by the time of storage: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB, and ALH. At 72 h of storage, sperm morphology was not different among treatments (P>0.05), showing an overall mean of 9.2 ± 0.36 total defects. In conclusion, the bithermic dilution makes the process of artificial insemination doses production faster by taking less time to reach a temperature close to that of storage, without impairing semen quality.

O uso de protocolos de diluição bitérmica está aumentando em centros de inseminação artificial e é necessário garantir que as doses de inseminação tenham a mesma qualidade quando comparado com protocolos de diluição isotérmica. Quatro ejaculados de cada 19 reprodutores PIC® foram coletados e distribuídos em split sample em três tratamentos: diluição bitérmica em duas etapas (T1), diluição isotérmica em duas etapas (T2) e diluição isotérmica em uma etapa (T3). A curva de temperatura para os três tratamentos foi feita utilizando um data logger com sensor de temperatura. As doses inseminantes foram preparadas utilizando o diluente BTS e armazenadas a 16ºC e usadas para avaliação dos parâmetros espermáticos através do Sistema CASA e avaliação de morfologia espermática, durante 120 horas. A temperatura das amostras de sêmen submetidas à diluição bitérmica em duas etapas alcançou 24,1ºC durante 120 minutos , enquanto que as amostras submetidas à diluição isotérmica em uma ou duas etapas alcançou 26,8ºC e 27,0ºC, respectivamente. A motilidade total, a progressiva e BCF foram influenciadas (P<0,05) pelo tempo de diluição, mas não pelo protocolo de diluição. A motilidade total e progressiva diminuiu com o tempo de armazenamento (91.0 ± 0.91 para 81.5 ± 1.08 % e 74.0 ± 2.48 para 60.4 ± 2.59% de 24h para 120h, para MOT e PROG, respectivamente) enquanto BCF diferiu entre 24 e 120h (28.6 ± 0.76 e 27.3 ± 0.79 Hz). As seguintes características de motilidade não foram afetadas pelo protocolo de diluição e pelo tempo de armazenamento: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB e ALH. Às 72 h de armazenamento, a morfologia espermática não diferiu entre os tratamentos (P>0.05), apresentando uma média geral de 9.2 ± 0.36 defeitos totais. Concluindo, a diluição bitérmica torna o processo de produção de doses inseminantes mais rápido, pois demoraram menos tempo para alcançar a temperatura próxima de armazenamento, sem comprometer a qualidade das doses inseminantes produzidas. / The use of bithermic dilution protocols is increasing in artificial insemination centers, being necessary to guarantee that the quality of insemination doses remain the same when compared to isothermic dilution protocols. Four ejaculates from each one of 19 crossbreed PIC® boars were collected and assigned, in a split sample design, in to three treatments: two step bithermic dilution (T1), two step isothermic dilution (T2) and one step isothermic dilution (T3). Temperature curve for the three treatments was recorded using a temperature sensor data logger. Semen doses prepared with BTS extender were stored at 16°C and were used to evaluate sperm parameters through CASA system and sperm morphology, during 120 h. The temperature in semen samples submitted to a two-step bithermic dilution reached 24.1ºC during 120 min, whereas one or two-step isothermic dilution samples reached 26.8ºC and 27.0ºC, respectively. Total motility, progressive motility and BCF were influenced (P<0.05) by the storage time but not by the dilution procedure. Total and progressive motility reduced throughout the storage time (91.0 ± 0.91 to 81.5 ± 1.08 % and 74.0 ± 2.48 to 60.4 ± 2.59% from 24h to 120h, for MOT and PROG respectively) whereas BCF differed between 24 and 120h (28.6 ± 0.76 and 27.3 ± 0.79 Hz). The following motility traits were neither affected by the dilution procedure nor by the time of storage: DAP, DCL, DSL, VAP, VCL, VSL, STR, LIN, WOB, and ALH. At 72 h of storage, sperm morphology was not different among treatments (P>0.05), showing an overall mean of 9.2 ± 0.36 total defects. In conclusion, the bithermic dilution makes the process of artificial insemination doses production faster by taking less time to reach a temperature close to that of storage, without impairing semen quality.