A novel approach to minimising acute equine endometritis that may help to prevent the development of the chronic state

One of the most commonly encountered challenges in equine breeding is endometritis, which can be difficult to resolve and causes considerable economic losses to the industry. It is a multifactorial condition, developing as an exaggerated form of the normal physiological response to breeding. Seminal plasma proteins, spermatozoa, bacteria and debris initiate an inflammatory response; the resulting fluid and neutrophils are then cleared from the uterus along with the debris. However, in some mares, the response is prolonged or exaggerated, with much fluid formation and neutrophil infiltration leading to acute endometritis. A bacterial cause has been implicated, although in some cases no pathogenic organisms can be isolated on culture. It has been postulated that any one of a variety of bacteria could be involved, or dysbiosis of the uterine microbiome could be responsible. Repeated episodes of acute endometritis may lead to the pathology associated with chronic endometritis, with mucociliary dysfunction, vascular degeneration and plasma cell infiltration. This review examines the information that is currently available about equine endometritis, particularly about the role of the inseminate in the uterus, and its current treatment. There are some promising lines of research into treatment or prevention that may help to resolve the issue

Associations between insulin-like factor 3, scrotal circumference and semen characteristics in young Norwegian Red bulls

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Novel interpretation of sperm stress test and morphology for maturity assessment of young Norwegian Red bulls

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Practical applications of sperm selection techniques for improving reproductive efficiency

Several selection techniques are available for processing spermatozoa. Apart from sperm washing to remove seminal plasma, only "swim-up" and colloid centrifugation have been used to any extent to prepare spermatozoa for in vitro fertilization, and only colloid centrifugation has been used to prepare sperm samples for artificial insemination. Single-layer centrifugation (SLC) through a species-specific colloid has been shown to be effective in selecting spermatozoa with good motility, normal morphology and intact chromatin in a range of species. This method is less timeconsuming than swim-up, and has been scaled-up to allow whole ejaculates to be processed in a practical manner. The applications of SLC are as follows: to improve sperm quality in insemination doses or in samples for in vitro fertilization, to increase the shelf life of normal sperm doses, to remove pathogens (viruses, bacteria), to improve cryosurvival by removing dead and dying spermatozoa before freezing or after thawing, to select spermatozoa for intracytoplasmic sperm injection, and to aid conservation breeding

Detection of subclinical mastitis in camels (Camelus dromedarius) using somatic cell count, N-acetyl-beta-D-glucosaminidase and lactate dehydrogenase activity

Clinical and subclinical mastitis (SCM), mostly related to intramammary infection (IMI), is prevalent in pastoralist camel herds. An IMI has implications for public and animal health as well as for household economy. As bacterial culturing is expensive, time consuming and impractical in a pastoralist setting, other early detection methods for SCM in camels need to be investigated. Somatic cell count (SCC) is the standard for detecting SCM in cattle. The udder health indicators of N-acetyl-beta-D-glucosaminidase (NAGase) and lactate dehydrogenase (LDH) activity are useful as diagnostic markers in cow, sheep and goat milk; they could be of potential use in camel milk production. The aim of this study was to improve the understanding of SCM in camels, and specifically to assess SCC, and NAGase- and LDH activity in camel milk. In addition, potential associations between SCM (defined by a California Mastitis Test (CMT) score >= 3 and no signs of clinical mastitis) and SCC, NAGase- and LDH activity were investigated.In total, 40 healthy camels without clinical mastitis were sampled in four herds in Kenya. Quarter milk samples were collected aseptically and screened using CMT. SCC was analysed using a direct cell counter (DCC, DeLaval), and NAGase and LDH activity was analysed using kinetic fluorometric measures.In total, 116 milk samples were tested with CMT and analysed for SCC. Of these, 88 were analysed further for NAGase and LDH. The median SCC was 151,000 cells/mL (IQR: 49,500-709,000 cells/mL), and median NAGase and LDH were 18.5 U/l (IQR:14.8-24.0 U/l) and 12.0 U/l (IQR: 8.5-16.2 U/l) respectively. All inflammatory markers (SCC, NAGase, LDH) were significantly associated with SCM (P < 0.001). In conclusion, SCC, NAGase and LDH are potential inflammatory indicators in camel milk that can be used for detection of udder quarters with SCM

New approach to assess sperm DNA fragmentation dynamics: Fine-tuning mathematical models

Background Sperm DNA fragmentation (sDF) has been proved to be an important parameter in order to predict in vitro the potential fertility of a semen sample. Colloid centrifugation could be a suitable technique to select those donkey sperm more resistant to DNA fragmentation after thawing. Previous studies have shown that to elucidate the latent damage of the DNA molecule, sDF should be assessed dynamically, where the rate of fragmentation between treatments indicates how resistant the DNA is to iatrogenic damage. The rate of fragmentation is calculated using the slope of a linear regression equation. However, it has not been studied if sDF dynamics fit this model. The objectives of this study were to evaluate the effect of different after-thawing centrifugation protocols on sperm DNA fragmentation and elucidate the most accurate mathematical model (linear regression, exponential or polynomial) for DNA fragmentation over time in frozen-thawed donkey semen. Results After submitting post-thaw semen samples to no centrifugation (UDC), sperm washing (SW) or single layer centrifugation (SLC) protocols, sDF values after 6 h of incubation were significantly lower in SLC samples than in SW or UDC. Coefficient of determination (R2) values were significantly higher for a second order polynomial model than for linear or exponential. The highest values for acceleration of fragmentation (aSDF) were obtained for SW, followed by SLC and UDC. Conclusion SLC after thawing seems to preserve longer DNA longevity in comparison to UDC and SW. Moreover, the fine-tuning of models has shown that sDF dynamics in frozen-thawed donkey semen fit a second order polynomial model, which implies that fragmentation rate is not constant and fragmentation acceleration must be taken into account to elucidate hidden damage in the DNA molecule

Extenders for alpaca epididymal spermatozoa: Comparison of INRA96 and andromed

Artificial insemination would be a useful technique for alpaca breeders to use as an aid to breeding to increase fleece quality. The technique, however, is not well developed in alpacas, partly because of the viscous nature of their seminal plasma. Castration conducted for husbandry purposes can provide a source of epididymal spermatozoa to test semen extenders or handling regimens, thus circumventing the problem of the viscous ejaculate. In this experiment, two semen extenders (Andromed and INRA96) developed for other species (bovine and equine, respectively) were tested with alpaca spermatozoa derived from the cauda epididymis. Sperm total motility (mean ± SEM A: 29.1 ± 4.8 % compared with I: 35.4 ± 4.8 %; NS), membrane integrity (A: 58 ± 9% compared with I: 56 ± 9%; NS) and acrosome integrity (A: 65 ± 7% compared with I: 54 ± 7%; NS) were not different between the two extenders. Progressive motility with use of INRA96 was greater after incubating for 30 min than after incubating for 10 min (35 ± 4% vs. 12 ± 4%, respectively; P = 0.03). In conclusion, viable epididymal spermatozoa could be extracted from the castrated organs after overnight transport. There were no differences in sperm quality between the two extenders; therefore, it appears that either extender could be used for alpaca spermatozoa. These results could help in the development of a technique for artificial insemination in alpacas

Testicular length as an indicator of the onset of sperm production in alpacas under Swedish conditions

Background: The popularity of alpacas (Vicugna pacos) is increasing in Sweden as well as in other countries; however, knowledge about optimal management practices under Swedish conditions is still limited. The wide age range reported when the onset of puberty can occur, between 1 and 3years of age, makes management decisions difficult and may be influenced by the conditions under which the alpacas are kept. The aim of this study was to find out when Swedish alpacas can be expected to start producing sperm, by using testicular length and body condition score as a more precise indirect indicator than age. Results: This study suggests that animals with a testicular length ≥3.8cm would be producing sperm; however, if it is crucial to know that there is no sperm production for management purposes, the threshold level for testicular length used to differentiate between sperm-producing and non-sperm producing animals should be ≤1.6cm instead. If only one variable is considered, testicular length appears to better than age alone to predict sperm production. Body condition score together with testicular length explains the individual onset of puberty and better guide management recommendations. Conclusions: Using a combination of these parameters (testicular length, body condition score and age) as a tool for decision making for alpaca husbandry under Swedish conditions is suggested