Low temperature preservation of porcine semen: influence of short antimicrobial lipopeptides on sperm quality and bacterial load

Antimicrobial resistance is a steadily increasing problem and poses a serious threat to global public health. Therefore, it is highly necessary to advance the development of novel antimicrobial compounds and semen preservation strategies. The aim of this study was to evaluate a low temperature, antibiotic-free preservation procedure using Androstar Premium (ASP) extender (Minitüb) with antimicrobial lipopeptides. Firstly, seven lipopeptides in two concentrations (1 × minimum inhibitory concentration (MIC)/2 × MIC) were tested on their sperm-compatibility at 17 °C. Two lipopeptides, C16-KKK-NH2 and C16-KKKK-NH2, did not negatively affect sperm quality and were further evaluated for their efficiency of bacterial growth inhibition at 5 °C. Besides an overall diminution of colony forming units, both peptides showed a reduction of bacterial subcultures (n = 103) with a decrement in Gram-positive rods from 65 (ASP w/o supplements) to 39/52 (ASP w/ C16-KKK-NH2/C16-KKKK-NH2), in Gram-positive cocci from 21 to 9/10 and in Gram-negative species from 17 to 8/5 total subcultures. Furthermore, lipopeptides revealed activity towards selected bacteria of potential concern in artificial insemination like Trueperella pyogenes, Alcaligenes faecalis, Pseudomonas aeruginosa (not C16-KKK-NH2), Pasteurella sp., Providencia stuartii, Escherichia coli (not C16-KKKK-NH2) and Streptococcus porcinus (not C16-KKKK-NH2). Consequently, both tested lipopeptides are promising candidates for alternative antibiotic-free preservation techniques of boar semen.

www.nature.com/scientificreports/ causing antibiotics to reach the liquid manure. Therefore, it is highly necessary to question the standardized supplementation of boar semen extenders with conventional antibiotics 6 . In the search for strategies to prevent antibiotic resistance, antimicrobial peptides (AMPs) and their potential to serve as a substitute for conventional antibiotics have been the focus of many research projects over the past ten years [8][9][10][11] . AMPs are a structurally diverse group of cationic, amphiphilic peptides. Bacteria are less likely to develop resistance towards AMPs than towards conventional antibiotics as the toxic pathways of AMPs often provoke cell lysis through unspecific disruption of the lipid bilayers rather than by an interaction with a specific target 12 . Ideally, AMPs used for boar semen preservation should possess the following criteria: (1) broad spectrum of antimicrobial action, (2) absence of sperm toxicity, (3) no interference with fertility, (4) high stability (for the entire storage duration of boar spermatozoa), (5) high activity at common semen storage temperatures, (6) low potential to evoke resistance, (7) ease of application and (8) economic feasibility 13 . Even though there have been promising results regarding the use of AMPs in AI in pigs, there are also many challenges, like the expensive and often time-consuming synthesis, insufficient antimicrobial activity or detrimental effects on sperm quality 14 . Another approach towards the waiving of antibiotics in the pig AI industry is the low temperature storage of extended boar spermatozoa, which helps to minimize bacterial growth 15 and could also help to reduce the development of multi-resistant bacteria with absent selection pressure of antibiotics.
Thus, the aim of the present study was to evaluate a holistic approach combining a low temperature, antibioticfree storing procedure for boar sperm with the use of alternative antimicrobial agents. The applied substances were a group of seven short lipopeptides derived from the two amino acid derivatives Fmoc-Lys(Boc)-OH and Fmoc-Lys(Fmoc)-OH 16,17 . Short lipopeptides possess many of the qualities of the more in-depth studied AMPs stated above (amphipathic, positively charged, antimicrobially active) while being less cost-and time-consuming in production 18 . All tested lipopeptides had a positive net charge of at least two and a supplemented fatty acid chain in order to create a proper balance between the hydrophilic and hydrophobic entities of the molecule, which is a crucial factor for their antimicrobial potency 17 . After testing the different lipopeptides on their influence on sperm quality, the combination of a cold-temperature storage at 5 °C with the addition of the most spermcompatible lipopeptides was examined on synergistic effects concerning the inhibition of bacterial growth and the preservation of a sufficient sperm quality in order to find possible alternatives for conventional antibiotics used in the pig AI industry.

Synthesis and purification of lipopeptides.
Seven short lipopeptides were assembled by solid-phase procedure using Fmoc chemistry on Fmoc-Rink Amide AM resin (0.48 mmol/g, IrisBiotech, Germany). Two amino acid derivatives, Fmoc-Lys(Boc)-OH and Fmoc-Lys(Fmoc)-OH (IrisBiotech, Germany), were used. The Fmoc group was detached by treating the resin with a solution of 20% piperidine in N, N -dimethylformamide for 20 min (two steps of 5 and 15 min). Peptide bond formation was conducted with 1,2-diisopropylcarbodiimide (DIC)/1-hydroxybenzotriazole (HOBt) in dimethylformamide (DMF)/dichloromethane (DCM) (50/50; v/v) during 120 min. After each coupling and deprotection step, the peptidyl-resin was washed (3 × DCM, 3 × DMF/ DCM, 3 × DCM). The deprotection and coupling reactions were monitored by the chloranil test. The final deprotection and cleavage of the lipopeptide from the solid support were performed with a solution of trifluoroacetic acid (TFA), triisopropylsilane (TIS) and water-TFA/TIS/water (90/2.5/2.5, v/v/v) for 120 min, at ambient temperature. After this, resin was filtered and the solution with cleaved lipopeptides was concentrated via rotary evaporator. The lipopeptides were then precipitated with diethyl ether and centrifuged. The precipitates were dissolved in water and freeze-dried (Christ, Germany). The lipopeptides were purified via reverse-phase high performance liquid chromatography (RP-HPLC) on a Knauer K1001 two-pump system (Knauer, Germany). For purification a semi-preparative column Nucleodur C18HTec (5 µm, 100 Å, 10 × 250 mm) was used (Macherey-Nagel, Germany). The lipopeptide compounds were eluted with a linear gradient with 20-60% of phase B (where phase A-0.1% TFA in water, phase B-0.1% TFA in acetonitrile), at a flow rate of 3 ml/min, at 214 nm for 120 min.
Reversed-phase analysis of lipopeptides. The lipopeptides were analysed via RP-HPLC on a Chromolith Performance RP18ec (100 × 4.6 mm) column (Merck, Germany) using a Shimadzu Prominence system with a linear gradient with 2-98% phase B (where phase A-0.1% TFA in water, phase B-0.1% TFA in acetonitrile), at a flow rate of 2 ml/min, at 214 nm. Identity and purity of the lipopeptides were verified by the matrix assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS, Biflex III, Bruker, Germany). The purity of the lipopeptides was established higher than 95%.
Experimental design. Two independent experiments (exp.) were conducted. In exp. 1, we evaluated potential detrimental effects of two concentrations of different lipopeptides on boar spermatozoa ( Table 1). The minimum inhibitory concentration (1 × MIC) and 2 × MIC, which were established in prior studies on a range of different bacterial species 17 , were used in antibiotic-free Beltsville Thawing Solution (BTS) extender ( www.nature.com/scientificreports/ In exp. 2, we examined the effects of 1 × MIC and 2 × MIC of two selected lipopeptides with the least negative impact on sperm quality, C16-KKK-NH 2 and C16-KKKK-NH 2 , in extended boar semen stored at 17 °C and/or 5 °C (Table 2). In this trial, we used the antibiotic-free Androstar Premium (ASP) long-term extender (in treatment groups and positive control w/o supplements) and a conventional BTS extender with gentamicin sulphate (0.25 g/l, negative control, stored at 17 °C only). Analyses were the same as in exp. 1. Additionally, aliquots for microbiological investigations were taken immediately after sample preparation (0 h), and after 24 h, 48 h and 72 h of storage. Animals, semen collection and transport. All procedures involving animals were carried out in accordance with guidelines and regulations according to the European Commission Directive for Pig Welfare and were approved by the animal welfare committee of the state of Brandenburg (TVO-2019-V-20). A total of 14 ejaculates from different mature, healthy Pietrain boars (age: 16.9 ± 4.5 months) of proven fertility from a single boar stud in Northern Germany were used (exp. 1: n = 6 ejaculates; exp. 2: n = 8 ejaculates). The boars were routinely used for AI, received commercial feed (pellets) for AI boars and were housed individually in straw-bedded pens equipped with nipple drinkers. Ejaculates were collected weekly by the gloved-hand method. The day of collection is specified as day 0 (0 h of storage). The pre-sperm phase of each ejaculate was discarded and the gel fraction of the semen was removed by gauze filtration during collection.
Normospermic ejaculates were diluted isothermically (33 °C) on split-sample basis in order to prepare the following split semen sample groups ( Table 2) according to extender type (BTS or ASP) and storage temperature (17 °C or 5 °C) using: BTS w/o antibiotics (exp. 1), BTS with gentamicin sulphate (0.25 g/L, control group in exp. 2) or Androstar Premium w/o antibiotics (2 nd control group and treatment group in exp. 2) to a concentration of 2.6 × 10 7 spermatozoa/ml (NucleoCounter SP-100, Chemometec, Denmark). Semen was filled in QuickTip Flexitubes (Minitüb) with an AI dose volume of 85 ± 1 ml. Samples for 17 °C storage were placed in a temperature-controlled box at 22 °C for 90 min. The temperature was then reduced to 17 °C (overall cooling rate 4 °C/hour) and samples were stored in a refrigerator at 17 °C in the dark. Samples for 5 °C storage were placed in a cardboard box with a lid together with isothermic (28 °C) water-filled tubes. Boxes were subsequently kept for 6 h at 22 °C and then stored in a refrigerator at 5 °C in the dark according to Waberski et al. 15 .  evaluation of boar sperm motility. Motility assessment was done using a computer-assisted semen analysis (CASA, AndroVision, Minitüb). Samples for thermo-resistance test were measured after 72 h of semen storage and a following incubation time of 30 min (TRT30) and 300 min (TRT300) at 38 °C according to Schulze et al. 19 . Subsamples of 3.0 µl each were placed in preheated Leja chambers (Leja Products B.V., Nieuw Vennep, The Netherlands) and at least 1,000 spermatozoa per sample were recorded. Spermatozoa were defined motile when showing an amplitude of lateral head displacement (ALH) > 1.0 µm and a velocity curved line (VCL) > 24.0 µm x s -1 . When VCL was ≥ 48.0 µm x s -1 and velocity straight line (VSL) was ≥ 10.0 µm x s -1 , they were listed as progressively motile spermatozoa. flow cytometric assessment of boar spermatozoa. All aliquots for analyses were taken after 72 h of storage and 30 min of incubation at 38 °C. Analyses were performed using CytoFLEX S (Beckman Coulter, Indianapolis, United States) equipped with a 488 nm and 525 nm diode laser. Fluorescence signals of FITC-PNA, FITC-PSA and R123, gathered via 525/40 nm BP filter, and PI, gathered via 610/20 nm BP filter, were plotted on logarithmic scales. The sperm population was gated referring to the expected forward-and side-scatter signals and a total of 10,000 events were counted in this area. For assessment of MITO, a double-staining with R123 and PI according to Schulze et al. 20 was done. To evaluate PMAI, a triple-staining with FITC-PNA, FITC-PSA and PI was done as described previously 21 . After incubation with fluorochromes, 30 µl of each sample were added to 2 ml of isotherm phosphate-buffered NaCl solution. The percentage of spermatozoa with active mitochondria (MITO) and the percentage of spermatozoa with intact acrosome and plasma membrane (PMAI) were recorded.
Microbiological analyses. In exp. 2, immediately after sampling (0 h) as well as after 24 h, 48 h and 72 h of semen storage, two aliquots of 1.5 ml per sample were taken from samples with lipopeptide supplementation in 1 × MIC as well as from 17 °C BTS w/ gentamicin and 5 °C ASP w/o supplements. Aliquots of extended semen were frozen with glycerol 5:1 (vol/vol) in liquid nitrogen before storage at -80 °C until analysis to protect bacterial cells from freeze-thaw damage 22 . To determine the total microbial count in extended semen samples, serial dilutions were prepared in PBS ranging from 10 -1 to 10 -2 . 100 µl of each dilution were plated on LB agar plates (LB medium from Carl Roth) in duplicates and incubated at 37 °C under aerobic conditions. Colony forming units (CFU)/ml were calculated after 48 h of incubation.
Bacterial isolations were performed from 10 µl of extended semen samples on a plate set routinely used for bacterial diagnostics (Columbia Agar with sheep blood, Gassner and UTI Clarity agar, all Oxoid Thermo Fisher, Wesel, Germany). The agar plates were incubated aerobically for 24 h at 37 °C and the initial blood agar plates were re-incubated for another 24 h at 37 °C under 5% CO 2 atmosphere to promote slow and fastidious growing bacterial species. After 24 h and 48 h incubation, distinct bacterial colonies were subcultured under identical conditions for bacterial identifications. Bacterial isolates were identified by standard diagnostic methods including the API identification system (BioMerieux, Nürtingen, Germany) and 16S rDNA gene analysis according to Mühldorfer et al. (2011) 23 . All subcultures were finally grouped into three major categories: (i) Gram-positive rods, (ii) Gram-positive cocci and (iii) Gram-negative species for comparison of the results. The grouping was necessary because of the diversity of the isolated bacterial species and several isolates that could not be fully classified to genus or species levels.
Statistical analysis. Data analysis was performed using SPSS Statistics 23 (IBM, Armonk, USA) and R (R Foundation for Statistical Computing, Vienna, Austria) 24 . Sperm quality characteristics in exp. 1 and 2 as well as the microbiological data were directly compared between each supplement and control. Data were tested on normal distribution (Shapiro-Wilk test) and variance homogeneity (Levene test) before choosing the appropriate paired test (normal, variance homogeneous: t-test, not homogeneous: Welch test, non-normal: Mann-Whitney-U test). The resulting significances are depicted in Figs. 1-3. To meet the requirements of repeated measures experimental design of exp. 2, a generalized linear mixed model was applied. Therefore, the AI boars were appointed as experimental samples (subjects) and the extender (BTS w/ gentamicin, ASP w/o supplements, ASP w/ C16-KKK-NH 2 , ASP w/ C16-KKKK-NH 2 ), the concentration (1 × MIC, 2 × MIC), the storage temperature (17 °C, 5 °C) and the incubation time (30 min, 300 min) were considered as fixed factors. Data are presented as boxplots. Differences were considered significant when the calculated probability of their occurrence was less than 5% (P < 0.05).  (Table 3, P = 0.001). The two tested lipopeptides C16-KKK-NH 2 and C16-KKKK-NH 2 did neither negatively affect progressive motility nor MITO or PMAI compared to BTS 17 °C (Table 3). Comparing ASP w/o supplements and ASP w/ lipopeptides, both AMPs significantly reduced progressively motile spermatozoa (Table 4, P = 0.019 and P = 0.012, respectively) and PMAI (both P = 0.001). Furthermore, C16-KKK-NH 2 reduced MITO when compared to ASP w/o supplements (Table 4, P = 0.021). The concentration of lipopeptides had a significant effect on PMAI. Here, it became apparent that 1 × MIC resulted in a higher percentage of membrane intact sper- www.nature.com/scientificreports/ matozoa (Table 3, P = 0.006) compared to 2 × MIC. Furthermore, the temperature had a significant effect with a reduction of the overall progressive motility, MITO and PMAI after storage at 5 °C (Table 3, each P < 0.001). Based on the differences from the mixed model, we performed a paired test between each variant and control shown in Fig. 2. In a direct comparison between lipopeptide supplemented samples and 17 °C BTS w/ gentamicin Table 3. Results of a generalized linear mixed model for the effect of different factors on progressive motility in a thermo-resistance test, mitochondria activity and membrane integrity of boar spermatozoa preserved for 72 h when compared to the negative control (BTS w/ gentamicin, 17 °C). The model included the extender (ASP w/o supplements) and lipopeptides (C16-KKK-NH 2 or C16-KKKK-NH 2 ), the concentration (0 × MIC / 1 × MIC / 2 × MIC), the temperature (5 °C / 17 °C) and the incubation time (30 min / 300 min) as fixed effects.
Microbiological results. Wide, boar-individual ranges of the total bacterial load were determined from the investigated samples (Fig. 3).  Table 5. The ASP extender w/o supplements at 5 °C (positive control) showed the highest number of distinct subcultures identified over all time points, with a total of 103 and a mean of 13, whereas the supplementation with C16-KKK-NH 2 and C16-KKKK-NH 2 resulted in a total of 56 and 67 distinct subcultures and a mean of 7 and 8, respectively. A reduction of the number of subcultures due to the lipopeptides was noticeable in all categories of bacteria, with a decrement from 65 to 39/52 total subcultures of Gram-positive rods, from 21 to 9/10 total subcultures of Gram-positive cocci and from 17 to 8/5 total subcultures of Gram-negative species, respectively.
Additionally, bacterial species of potential concern for AI were recorded (Table 6). This category included species that could negatively impair the spermatozoa or bear specific risks in semen production 25 , such as potential extended spectrum beta-lactamase (ESBL) or biofilm producing bacteria, as well as species that can cause bacterial infections in sows. The following species from this category were identified in ASP-extended semen samples: Trueperella pyogenes, Streptococcus (S.) porcinus, Alcaligenes faecalis, Pseudomonas (P.) aeruginosa, Pasteurella sp., Providencia stuartii and Escherichia (E.) coli. They were also isolated from the positive control (ASP 5 °C w/o lipopeptides) with the exception of E. coli. In samples supplemented with C16-KKKK-NH 2 , only S. porcinus and E. coli were detected, and in samples containing C16-KKK-NH 2 only P. aeruginosa was found.

Discussion
Currently, the pig AI industry is heavily relying on the routine use of antibiotics in semen preservation in order to maintain high standards of sperm quality from production to insemination. The steadily increasing threat of antimicrobial resistance, however, is an urgent matter that calls for plans of action in all related areas of concern. The possibility of a boar semen preservation procedure that could forgo the use of antibiotics while still maintaining satisfactory sperm quality would therefore be an important step in combatting multidrug-resistant bacteria. The aim of our study was to investigate, whether the combination of a low temperature storage at 5 °C with the use of lipopeptides as alternative antimicrobial supplements could meet these conditions. The results of exp. 1 revealed that five out of seven lipopeptides impaired more than one of the tested sperm characteristics in a significant matter and were therefore excluded from the follow-up experiment. The effects were concentration-dependent, as 2 × MIC had more severe negative effects than 1 × MIC on sperm quality. This observation is in accordance with other studies implying that the concentration in which the AMPs are applied is an important determining factor for the sperm compatibility of antimicrobial agents 26 . A probable reason for the interference of five of the tested lipopeptides with sperm quality is their antimicrobial mode of action, which not only targets unwanted bacteria, but also negatively impacts sperm physiology and therefore prohibits their use in semen preservation.
There are different assumptions as to how AMPs operate on a molecular level. Regarding their primary mode of action, AMPs can be classified as either membrane targeting or non-membrane targeting 27,28 . In most cases, membrane targeting ultimately leads to an increase in membrane permeability and thus deregulation of the membrane potential 29,30 . The observations from exp. 1 show that the membrane integrity of spermatozoa was severely affected by almost all tested lipopeptides, suggesting that the cytotoxic effects on the spermatozoa are based on membrane-targeting peptide properties. It is very likely that the same mechanism can be assumed for their interaction with bacteria. In general, the two most important factors for the membrane selectivity of AMPs towards prokaryotic cells are the electrostatic interaction between the cationic peptide and the highly acidic bacterial membrane, and secondly the presence of a relatively high amount of membrane-stabilizing cholesterol in eukaryotic cells, causing a higher rigidity of the lipid bilayer and thus inhibiting membrane disruption through   Table 6. Bacterial species of potential concern in artificial insemination identified from ASP samples w/o supplementation (positive control) and from ASP samples with lipopeptide supplementation (C16-KKK-NH 2 or C16-KKKK-NH 2 in 1 × MIC) after storage at 5 °C for 72 h. The frequency of each species as well as the sum and the percentage in proportion to the total subcultures are shown.

Bacteria ASP w/o supplements ASP w/ C16-KKK-NH 2 ASP w/ C16-KKKK-NH 2
Trueperella pyogenes 1 www.nature.com/scientificreports/ AMPs 12 . However, due to their relatively low ratio of membrane cholesterol to membrane phospholipids and the exposure of anionic sulfogalactosylglycerolipid on the sperm surface, boar sperm cells are more likely to be targeted by membrane-active AMPs than most other eukaryotic cells 14 . Again, this became apparent when five out of the seven tested lipopeptides caused sperm quality impairment to a non-acceptable degree. Two lipopeptides (C16-KKK-NH 2 and C16-KKKK-NH 2 ) from this study impaired the sperm quality less severely than the other five. Interestingly, both belonged to the group of lipopeptides with the lowest MIC against tested control bacteria 18,31 , suggesting, that the reason for their sperm-compatibility was not an overall lower efficiency or activity, but rather a higher and more specific target selectivity. While there is evidence in prior studies suggesting that the effect of the two selected lipopeptides results from a more complex mode of action than a simple detergent-like membrane disruption, their intricate mechanism is yet to be discovered 32 . Nevertheless, AMPs bear a high potential to be applied as additives in semen preservation, when carefully selected on the basis of their antimicrobial mechanism of action and membrane selectivity.
A second important approach for antibiotic-free boar semen storage is the possibility of a low temperature preservation, which has been studied extensively but with limited success due to the high cold shock susceptibility of boar semen 4,33 . The most important mechanism for sperm quality loss due to lower storage temperatures is the lipid phase transition of the cell membrane 34 . Boar sperm are more prone to cold shock than sperm of many other species because of their relatively low concentration of membrane stabilizing cholesterol. However, the susceptibility for cold shock is dependent on many different factors, and recently there have been reports of successfully sustained sperm quality at low temperature through optimization of surrounding conditions 15,35,36 . Amongst others, boar individual eligibility 37,38 , the cooling rate 15,39 , the used extender 40 , motionless storage 41 and transport 42 play important roles in the maintenance of sperm quality.
Androstar Premium extender was used just as in other studies, where boar sperm were successfully stored at 5 °C 15,35 . Even though the precise composition of this extender is not revealed by the manufacturers, it is anticipated that membrane stabilizers and capacitation inhibitors help to preserve sperm quality for longer periods of time or in less favourable surrounding conditions. Our results support these propositions as samples stored in ASP showed significantly better sperm characteristics compared to BTS.
When considering the influence of the temperature, calculated with the linear mixed model, a "chillinginduced" negative effect on sperm cells became apparent. However, in a direct comparison of each 5 °C lipopeptide variant to the 17 °C BTS control w/ gentamicin (AI standard), no significant differences in progressive sperm motility could be found after thermo-resistance test, suggesting that surrounding conditions in the extender play an important role in the feasibility of a low temperature storage for commercial use. This observation can be considered a very positive effect, as the thermo-resistance is a sensitive fertility predictor, reflecting the relatively long period of exposure to 38 °C that spermatozoa face in the female reproduction tract before fertilization 20 . Furthermore, it is worth mentioning, that the mean progressive motility of all samples stored at 5 °C after 30 min incubation at 38 °C met the standard cut-off criteria (> 65% for sperm motility after 3 days of storage) for AI in Germany 43 . One could therefore conclude that, though accompanied by a slight impairment of certain quality characteristics, low temperature storage is still a feasible possibility, as the overall sperm quality is preserved to a satisfactory degree.
Another important factor that needs to be considered aside from the sperm quality is the effect of the chosen semen storage procedure on the bacterial load. It can be assumed that each AI dose has a basic bacterial content, since it is almost impossible to obtain a germ-free ejaculate. On average, boar ejaculates are loaded with 10 3 -10 5 CFU/ml of bacteria 25 , but bacterial numbers are highly influenced by the experimental conditions such as study design, the breed and age of the boar, as well as the method of ejaculate collection 44,45 . The causes for initial bacterial contamination can be animal-and / or environment-associated 46,47 . Therefore, the goal is not necessarily the production of sterile AI doses but rather adequate hygiene measures and the reduction of bacterial growth during storage through effective antibacterial means. Standard storing procedures reach this goal by the supplementation of antibiotics according to legal guidelines (Council Directive, European Union, 90/429/EEC).
Even though the use of BTS extender w/ gentamicin resulted in the lowest amount of CFU/ml, the number of bacteria in samples supplemented with one of the two selected lipopeptides was below the critical value of 10 3 CFU/ml 3,43 at all tested time points. Furthermore, both lipopeptides and particularly the C16-KKKK-NH 2 lipopeptide showed a selective effect on Gram-negative bacterial species, including ones often found in pig AI centers 2,25 . Additionally, the analysis regarding selected common species of concern in AI also showed that both lipopeptides clearly reduced the number of relevant Gram-negative and Gram-positive bacterial species from six (ASP w/o) to only two (C16-KKKK-NH 2 ) or one (C16-KKK-NH 2 ) compared to the controls, which are promising results for their antibacterial activity. Prior studies with similar lipopeptides support these findings, demonstrating that lipopeptides inhibit the growth of both Gram-positive and Gram-negative bacteria 48 and the overall antimicrobial activity appeared to be dependent on the length of the hydrophobic chains and the amount of lysine residues 32 .
In conclusion, an antibiotic-free low temperature preservation of boar semen at 5 °C supplemented with one of the two selected lipopeptides would be possible with only minor impairments when compared to the standard preservation at 17 °C in BTS containing antibiotics. These limitations include a slightly impeded sperm quality due to the low temperature storage and a slightly higher bacterial load. Nevertheless, the results were still within the quality requirements for AI doses worldwide 43 , and the abstain from the use of antibiotics should be considered the most compelling argument in comparison to these minor quality impairments.