Abstract:By controlling the growth of bacteria in extended koala semen, penicillin G and gentamicin are likely to lengthen the period by which spermatozoa can be stored at 16 degrees C and reduce the possibility of disease transmission during artificial insemination procedures.
“…Studies describing the use of antimicrobials in the preservation of semen from wild animals ( Table 1) are even more scarce than in companion animals. The combination of penicillin (1000 IU/mL) and gentamicin (100 μg/mL) was effective at preserving koala semen (Phascolarctos cinereus) at 16 °C for 24 h as it prevented bacterial growth without interfering on the sperm motility (Johnston et al, 1998). Additionally, the addition of gentamicin (70 μg / mL) (Santos et al, 2019a) and a combination of penicillin (2000 IU/mL and 1000 IU/mL)-streptomycin (2 mg/mL and 1 mg/mL) (Santos et al, 2019b) to the semen of collared peccaries (Pecari tajacu) allowed the control of bacterial growth in the samples and did not present toxic effects on the quality of the chilled semen maintained up to 36 h. Due to the differential action of antimicrobial substances in the distinct species, various studies have been conducted in order to stablish appropriate antimicrobial concentrations in the diluent.…”
Section: Use Of Antibacterial Substances In Semen Extendersmentioning
How to cite: Santos CS, Silva AR. Current and alternative trends in antibacterial agents used in mammalian semen technology.
AbstractThe use of antibacterial substances as additives in extenders for ensuring the sanitary quality of the semen employed in reproductive biotechniques and preserving it from bacterial deterioration has been reported since the mid-twentieth century. However, the deleterious effects of these drugs on the sperm quality as well as their effectiveness in controlling bacterial growth in the preserved semen have been questioned. The aim of this review was to report the antimicrobials primarily used in the extenders added to the semen of mammals, and to present alternatives to their use. Among the various mammalian species, there is a large variation regarding the antimicrobial types added to semen extenders as cephalosporins (ceftiofur, cefdinir, eg) and quinolones (ofloxacin, ciprofloxacin), alone or in combination with large action spectra substances as penicillin-streptomycin and gentamicin-tylosin-lincomycin-spectinomycin. To combat problems related to bacterial resistance to these drugs, the emergence of alternatives is increasingly evident. Among these alternatives, use of physical methods as centrifugation and filtration, as well as the use of antimicrobial peptides and other substances from different origins have been highlighted for presenting antimicrobial potential.
“…Studies describing the use of antimicrobials in the preservation of semen from wild animals ( Table 1) are even more scarce than in companion animals. The combination of penicillin (1000 IU/mL) and gentamicin (100 μg/mL) was effective at preserving koala semen (Phascolarctos cinereus) at 16 °C for 24 h as it prevented bacterial growth without interfering on the sperm motility (Johnston et al, 1998). Additionally, the addition of gentamicin (70 μg / mL) (Santos et al, 2019a) and a combination of penicillin (2000 IU/mL and 1000 IU/mL)-streptomycin (2 mg/mL and 1 mg/mL) (Santos et al, 2019b) to the semen of collared peccaries (Pecari tajacu) allowed the control of bacterial growth in the samples and did not present toxic effects on the quality of the chilled semen maintained up to 36 h. Due to the differential action of antimicrobial substances in the distinct species, various studies have been conducted in order to stablish appropriate antimicrobial concentrations in the diluent.…”
Section: Use Of Antibacterial Substances In Semen Extendersmentioning
How to cite: Santos CS, Silva AR. Current and alternative trends in antibacterial agents used in mammalian semen technology.
AbstractThe use of antibacterial substances as additives in extenders for ensuring the sanitary quality of the semen employed in reproductive biotechniques and preserving it from bacterial deterioration has been reported since the mid-twentieth century. However, the deleterious effects of these drugs on the sperm quality as well as their effectiveness in controlling bacterial growth in the preserved semen have been questioned. The aim of this review was to report the antimicrobials primarily used in the extenders added to the semen of mammals, and to present alternatives to their use. Among the various mammalian species, there is a large variation regarding the antimicrobial types added to semen extenders as cephalosporins (ceftiofur, cefdinir, eg) and quinolones (ofloxacin, ciprofloxacin), alone or in combination with large action spectra substances as penicillin-streptomycin and gentamicin-tylosin-lincomycin-spectinomycin. To combat problems related to bacterial resistance to these drugs, the emergence of alternatives is increasingly evident. Among these alternatives, use of physical methods as centrifugation and filtration, as well as the use of antimicrobial peptides and other substances from different origins have been highlighted for presenting antimicrobial potential.
“…In an attempt to improve our basic knowledge and thereby facilitate the management of wild and captive Koala populations, a series of studies, critical to the development of an AT programme, was carried out (Johnston, 1999). Three key areas were investigated: (1) semen collection (Johnston et al, , 1997a and preservation (Johnston et al, 1992(Johnston et al, , 1993(Johnston et al, , 1998(Johnston et al, , 2000a, (2) detection of oestrus and the timing of ovulation (Johnston et al, 2000b) and (3) anatomy of the 9 reproductive tract to determine the most appropriate site for the deposition of semen (Johnston, 1999).…”
Section: Development Of Artificial Insemination Techniquesmentioning
This paper documents the successful development of an artificial insemination (AI) programme for the Koala Phascolurctos cinereus. The protocols for trials involving two methods to induce ovulation and two insemination techniques are described. In Trial 1, interrupted coitus using a ‘teaser’♂ successfully induced ovulation in nine Koalas. Five ♀♀ were inseminated while conscious using a modified ‘foley catheter’ (Cook insemination catheter) resulting in the births of two offspring. The other four ♀♀ were anaesthetized and inseminated using a technique which allowed visualization of the most cranial portion of the urogenital sinus, where semen was deposited using a 3.5 Fr. ‘Tom‐cat catheter’ (urogen‐itoscopic insemination). Three of the four ♀♀ inseminated by this technique produced pouch young. Microsatellite analysis of DNA from the pouch young excluded the teaser ♀♀ as possible sires, confirming that all offspring were sired by donor sperm. In Trial 2, eight ♀♀ were induced to ovulate by injecting them with 250 International Units of human chorionic gonadotrophin (hCG). A luteal phase was confirmed in all eight ♀♀ but only one gave birth following urogenitoscopic insemination. The Koala pouch young in this study are the first of any marsupial to be conceived and born following A1 procedures. Details of the A1 procedures used are presented and the significance of A1 to the conservation biology of P. cinereus discussed.
“…To maintain some degree of long-term sperm preservation in the koala, it was found that their semen can be extended with the addition of Tris-citrate Glucose (TCG) when held at 5 °C (Johnston et al, 2000c), with the addition of antibiotics (penicillin G and gentamicin) to control the growth of bacteria (Johnston et al, 1998). Finally, more advanced methods to determine sperm integrity and fertilisation capacity have been developed, so that assessment of sperm quality is no longer based on motility alone.…”
Section: Assisted Breeding Technologies In Koala Conservationmentioning
confidence: 99%
“…All semen was collected by means of electro-ejaculation (EJ) while the koala was under a surgical plane of anaesthesia, using procedures previously described in detail by Johnston et al (2000a) All koala ejaculates were immediately diluted 1:1 with room temperature TCG buffer after collection; the TCG was composed of 3.0 g Tris base (Sigma Aldrich, Australia), 1.7 g citric acid (Sigma Aldrich, Australia) and 1.25 g glucose (Sigma Aldrich, Australia), made up to 100 mL with Milli-Q Ultrapure water (Millipore Australia Pty Ltd., North Ryde, NSW, Australia) and adjusted to a pH of 7.4 (Johnston et al, 2006). Unless otherwise stated, the TCG also contained penicillin G and gentamicin (Sigma Aldrich) at 1000 IU mL -1 and 100 µg mL -1 , respectively (Johnston et al, 1998).…”
Section: Koala Samples and Semen Collection And Preparationmentioning
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