Reindl Anita, Dzieciol Monika, Hein Ingeborg, Wagner Martin, Zangerl Peter
Institute for Milk Hygiene, Department for Farm Animals and Veterinary Public Health, Veterinärplatz 1, 1210 Vienna, Austria; Federal Institute for Alpine Dairying, Rotholz 50A, 6200 Jenbach, Austria.
Institute for Milk Hygiene, Department for Farm Animals and Veterinary Public Health, Veterinärplatz 1, 1210 Vienna, Austria.
J Dairy Sci. 2014 Oct;97(10):6036-45. doi: 10.3168/jds.2014-8218. Epub 2014 Aug 14.
A membrane filtration technique developed for counting butyric acid bacteria in cow milk was further developed for analysis of goat milk. Reduction of the sample volume, prolongation of incubation time after addition of proteolytic enzyme and detergent, and a novel step of ultrasonic treatment during incubation allowed filtration of goat milk even in the case of somatic cell counts (SCC) exceeding 10(6)/mL. However, filterability was impaired in milk from goats in late lactation. In total, spore counts were assessed in 329 farm bulk goat milk samples. Membrane filtration technique counts were lower than numbers revealed by the classic most probable number technique. Thus, method-specific thresholds for milk to evaluate the risk of late blowing have to be set. As expected, the spore counts of milk samples from suppliers not feeding silage were significantly lower than the spore counts of milk samples from suppliers using silage feeds. Not only were counts different, the clostridial spore population also varied significantly. By using 16S rRNA gene PCR and gene sequencing, 342 strains from 15 clostridial species were identified. The most common Clostridium species were Clostridium tyrobutyricum (40.4%), Clostridium sporogenes (38.3%), Clostridium bifermentans (7.6%), and Clostridium perfringens (5.3%). The 2 most frequently occurring species C. tyrobutyricum and C. sporogenes accounted for 84.7% of the isolates derived from samples of suppliers feeding silage (n=288). In contrast, in samples from suppliers without silage feeding (n=55), these species were detected in only 45.5% of the isolates.
一种为计数牛奶中丁酸菌而开发的膜过滤技术被进一步改进用于山羊奶分析。减少样品体积、在添加蛋白水解酶和去污剂后延长孵育时间,以及在孵育期间增加超声处理这一新颖步骤,使得即使在体细胞计数(SCC)超过10(6)/mL的情况下也能对山羊奶进行过滤。然而,处于泌乳后期的山羊所产牛奶的过滤性会受到损害。总共对329份农场散装山羊奶样品进行了孢子计数评估。膜过滤技术计数低于经典的最可能数技术所显示的数量。因此,必须设定针对牛奶的特定方法阈值以评估后期产气的风险。正如预期的那样,不喂青贮饲料的供应商所提供牛奶样品的孢子计数显著低于使用青贮饲料的供应商所提供牛奶样品的孢子计数。不仅计数不同,梭菌孢子菌群也有显著差异。通过使用16S rRNA基因PCR和基因测序,鉴定出了来自15种梭菌的342株菌株。最常见的梭菌种类是酪丁酸梭菌(40.4%)、生孢梭菌(38.3%)、双酶梭菌(7.6%)和产气荚膜梭菌(5.3%)。两种最常见的菌种酪丁酸梭菌和生孢梭菌占来自喂青贮饲料供应商样品(n = 288)分离株的84.7%。相比之下,在不喂青贮饲料供应商的样品(n = 55)中,这些菌种仅在45.5%的分离株中被检测到。