Plassard Vincent, Gisbert Philippe, Granier Sophie A, Millemann Yves
Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
Ceva Santé Animale, Libourne, France.
Front Vet Sci. 2021 Feb 10;8:633598. doi: 10.3389/fvets.2021.633598. eCollection 2021.
The aim of this work was to test a surveillance protocol able to detect extended-spectrum β-lactamase (ESBL)-, cephalosporinase (AmpC)- and carbapenemase (CP)-producing gram-negative bacteria in three conveniently chosen dairy farms with known prior occurrences of ESBL- and CP-producing strains. The protocol was applied monthly for a year. At each visit, 10 healthy lactating dairy cows were rectally swabbed, and raw milk filters (RMFs) were sampled in two of the three farms. Bacterial isolation was based on a first screening step with MacConkey agar supplemented with 1 mg/L cefotaxime and commercial carbapenem-supplemented media. We failed to detect CP-producing strains but showed that ESBL- strains, found in one farm only (13 strains), were closely associated with multi-drug resistance (12 out of 13). The limited number of conveniently selected farms and the fact that RMFs could not be retrieved from one of them limit the validity of our findings. Still, our results illustrate that ESBL-status changes monthly based on fecal swabs and negative herds should be qualified as "unsuspected" as proposed by previous authors. Although surveillance of farm statuses based on RMF analysis could theoretically allow for a better sensitivity than individual swabs, we failed to illustrate it as both farms where RMFs could be retrieved were constantly negative. Determination of CP herd-level status based on RMFs and our surveillance protocol was hindered by the presence of intrinsically resistant bacteria or strains cumulating multiple non-CP resistance mechanisms which means our protocol is not specific enough for routine monitoring of CP in dairy farms.
这项工作的目的是在三个方便选取的、已知先前存在产超广谱β-内酰胺酶(ESBL)和产碳青霉烯酶(CP)菌株的奶牛场,测试一种能够检测产ESBL、头孢菌素酶(AmpC)和CP的革兰氏阴性菌的监测方案。该方案每月应用一次,持续一年。每次走访时,对10头健康的泌乳奶牛进行直肠拭子采样,并在其中两个奶牛场采集生奶过滤器(RMF)样本。细菌分离基于第一步筛选,使用添加了1 mg/L头孢噻肟的麦康凯琼脂和添加了碳青霉烯类的商业培养基。我们未能检测出产CP菌株,但发现仅在一个奶牛场中发现的产ESBL菌株(13株)与多重耐药密切相关(13株中有12株)。方便选取的农场数量有限,以及其中一个农场无法获取RMF样本这一事实,限制了我们研究结果的有效性。尽管如此,我们的结果表明,根据粪便拭子检测,ESBL状态每月都会发生变化,阴性牛群应如先前作者所提议的那样被认定为“未受怀疑”。虽然理论上基于RMF分析监测农场状态可能比个体拭子检测具有更高的灵敏度,但我们未能证实这一点,因为两个能够获取RMF样本的农场一直呈阴性。基于RMF和我们的监测方案确定CP牛群水平状态受到固有耐药菌或累积多种非CP耐药机制的菌株的阻碍,这意味着我们的方案对于奶牛场CP的常规监测不够特异。