Head C B, Whitty D A, Ratnam S
J Clin Microbiol. 1982 Oct;16(4):615-21. doi: 10.1128/jcm.16.4.615-621.1982.
To determine the relative efficacy of pectin agar, cellobiose-arginine-lysine (CAL) agar, Y medium, cefsulodin-irgasan-novobiocin (CIN) agar, MacConkey (MAC) agar, and salmonella-shigella (SS) agar for the recovery of Yersinia enterocolitica, 35 strains of this organism representing the serotypes most commonly associated with human disease in Canada and the United States were inoculated on test media in pure cultures and mixed in fecal specimens. Randomly picked stool specimens were also cultured on these media to determine their selectivity. The ability of test media to support the growth of Y. enterocolitica strains varied markedly. Several strains failed to grow on Y medium, and a few failed to grow on SS agar. There were no significant differences in cultural characteristics and the recovery rates of Canadian and American strains. The combined recovery of the pure cultures of Y. enterocolitica on test media as compared with blood agar was MAC, 75%; SS, 48%; pectin, 70%; CAL, 62%; Y, 15%; and CIN, 85%. The selectivity of the test media expressed as the percent difference of the fecal colony counts obtained on blood agar and the selective media was MAC, 7%; SS, 50%; pectin, 4%; CAL, 65%; Y, >/=99.9%; and CIN, 95%. When stool suspensions containing 10(2) colony-forming units of the test strains were plated, CIN medium yielded 100% recovery of all 35 strains from all fecal samples. The combined recovery rate for other media was CAL, 63%; Y, 14%; and SS, 11%. With 10(1) colony-forming units, CIN yielded a 100% recovery of the test strains, whereas CAL, Y, and SS agar showed a 0% recovery. None of the test organisms was recovered on either MAC or pectin agar at either dilution. The inhibitory effect of Y medium for Y. enterocolitica could be overcome to some extent by reducing the sodium oxalate and sodium desoxycholate content of the medium. One such modified Y medium offered optimum selectivity and ensured greater recovery of Y. enterocolitica when compared with the Y medium. We found CIN agar by far the most effective medium for the recovery of Y. enterocolitica. This medium was highly selective and almost completely inhibited the fecal flora, while at the same time supporting luxuriant growth of Y. enterocolitica. On CIN agar, Y. enterocolitica colonies were distinctive in appearance and measured 1.5 to 4 mm in diameter within 20 to 40 h of incubation.
为确定果胶琼脂、纤维二糖 - 精氨酸 - 赖氨酸(CAL)琼脂、Y 培养基、头孢磺啶 - 伊红 - 新生霉素(CIN)琼脂、麦康凯(MAC)琼脂和沙门氏菌 - 志贺氏菌(SS)琼脂对小肠结肠炎耶尔森菌的分离效果,将 35 株代表加拿大和美国最常与人类疾病相关血清型的该菌纯培养物接种于试验培养基,并混入粪便标本中。还将随机选取的粪便标本接种于这些培养基上以测定其选择性。试验培养基支持小肠结肠炎耶尔森菌生长的能力差异显著。数株菌在 Y 培养基上不能生长,少数菌在 SS 琼脂上不能生长。加拿大菌株和美国菌株的培养特性及分离率无显著差异。与血琼脂相比,试验培养基上小肠结肠炎耶尔森菌纯培养物的综合分离率为:MAC 75%;SS 48%;果胶 70%;CAL 62%;Y 15%;CIN 85%。试验培养基的选择性以血琼脂和选择性培养基上粪便菌落计数的百分比差异表示为:MAC 7%;SS 50%;果胶 4%;CAL 65%;Y≥99.9%;CIN 95%。当接种含 10² 个试验菌株菌落形成单位的粪便悬液时,CIN 培养基从所有粪便样本中分离出全部 35 株菌,分离率达 100%。其他培养基的综合分离率为:CAL 63%;Y 14%;SS 11%。接种含 10¹ 个菌落形成单位时,CIN 培养基分离试验菌株的分离率为 100%,而 CAL、Y 和 SS 琼脂的分离率为 0%。在两种稀释度下,试验菌在 MAC 或果胶琼脂上均未分离出。通过降低培养基中草酸钠和去氧胆酸钠的含量,Y 培养基对小肠结肠炎耶尔森菌的抑制作用可在一定程度上被克服。一种改良的 Y 培养基与 Y 培养基相比具有最佳选择性,并确保了小肠结肠炎耶尔森菌的更高分离率。我们发现 CIN 琼脂是分离小肠结肠炎耶尔森菌最有效的培养基。该培养基具有高度选择性,几乎完全抑制粪便菌群,同时支持小肠结肠炎耶尔森菌旺盛生长。在 CIN 琼脂上,小肠结肠炎耶尔森菌菌落在孵育 20 至 40 小时内直径为 1.5 至 4 毫米,外观独特。