Evidence and antibiotic resistance profiles of clinical Acinetobacter calcoaceticus-Acinetobacter baumannii (ACB) and non-ACB complex members in companion animals: A 2020–2022 retrospective study

IF 2 3区 农林科学 Q4 IMMUNOLOGY Comparative Immunology Microbiology and Infectious Diseases Pub Date : 2024-04-17 DOI:10.1016/j.cimid.2024.102185
Anna-Rita Attili , Francesca Paola Nocera , Martina Sisto , Martina Linardi , Francesca Gigli , Victor Ngu Ngwa , Filomena Fiorito , Claudia Cerracchio , Marina C.T. Meligrana , Eleonora Bonacucina , Vincenzo Cuteri , Luisa De Martino
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Abstract

To evaluate the frequency of Acinetobacter spp., belonging to both Acinetobacter calcoaceticus-baumannii (ACB) and non-ACB complex, and their antibiotic resistance profiles in veterinary medicine, a three-year (2020–2022) retrospective study was carried out on sick companion animals. Epidemiological data from different clinical canine, feline, and equine samples, were acquired. For each strain, MALDI-TOF MS identification and susceptibility to a panel of 11 antibiotics, by Kirby-Bauer and E-test methods, were performed. Out of 628 bacteriological examinations, 2.5% resulted positive for strains belonging to Acinetobacter genus. Frequencies of 2.3%, 1.9%, and 3% were obtained from both in-visiting and hospitalized dogs, cats, and horses, respectively. Members of ACB-complex accounted for 50% of isolates. Since all strains resulted susceptible to aminoglycosides and polymyxins, no pandrug-resistant (PDR) species were recorded. While 12.5% A. baumannii resulted extensively-drug resistant (XDR), a higher percentage of multidrug-resistant strains was recorded among non-ACB strains (35.5%) than ACB strains (25%). Susceptibility was observed in the same percentage in both groups (62.5%). All ACB strains confirmed their intrinsic resistances. Non-ACB species showed lower resistances against antipseudomonal penicillins plus beta-lactamase inhibitors (P=0.1306), III generation cephalosporins (P=0.0547), and tetracyclines (P=0.0209) than ACB species. Carbapenem-resistance was observed for XDR A. baumannii (12.5%) and, in particular for MDR non-ACB complex members (25%). To our knowledge, A. lactucae represents the first description in two sick dogs in Italy. Furthermore, our results emphasize the role of non-ACB-complex species as important zoonotic pathogens, which could be reservoirs of clinically relevant resistance profiles.

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伴侣动物中临床醋酸钙不动杆菌-鲍曼不动杆菌(ACB)和非 ACB 复合体成员的证据和抗生素耐药性概况:2020-2022 年回顾性研究
为了评估醋酸钙化杆菌-鲍曼尼氏菌(ACB)和非 ACB 复合菌中醋酸钙化杆菌属的频率及其在兽医学中的抗生素耐药性情况,我们对生病的伴侣动物进行了一项为期三年(2020-2022 年)的回顾性研究。研究人员从不同的犬科、猫科和马科临床样本中获取了流行病学数据。通过柯比鲍尔法和 E 测试法,对每个菌株进行了 MALDI-TOF MS 鉴定和对 11 种抗生素的敏感性测试。在 628 次细菌学检查中,2.5% 的阳性菌株属于醋酸杆菌属。在就诊和住院的狗、猫和马身上发现的频率分别为 2.3%、1.9% 和 3%。ACB 复合菌株占分离菌株的 50%。由于所有菌株都对氨基糖苷类和多粘菌素类药物敏感,因此没有发现对潘生丁类药物(PDR)耐药的菌株。12.5%的鲍曼尼氏菌具有广泛耐药性(XDR),非 ACB 菌株(35.5%)中耐多种药物菌株的比例高于 ACB 菌株(25%)。两组菌株的敏感性比例相同(62.5%)。所有 ACB 菌株都证实了其固有的抗药性。与 ACB 菌株相比,非 ACB 菌株对抗假青霉素加 beta-内酰胺酶抑制剂(P=0.1306)、III 代头孢菌素(P=0.0547)和四环素(P=0.0209)的耐药性较低。XDR鲍曼不动杆菌(12.5%)对碳青霉烯类耐药,特别是MDR非ACB复合菌株(25%)对碳青霉烯类耐药。据我们所知,乳酸杆菌是首次在意大利的两只病犬中发现。此外,我们的研究结果还强调了非 ACB 复合菌种作为重要的人畜共患病原体的作用,它们可能是临床相关耐药谱的储存库。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
102
审稿时长
40 days
期刊介绍: Comparative Immunology, Microbiology & Infectious Diseases aims to respond to the concept of "One Medicine" and to provide a venue for scientific exchange. Based on the concept of "Comparative Medicine" interdisciplinary cooperation between specialists in human and animal medicine is of mutual interest and benefit. Therefore, there is need to combine the respective interest of physicians, veterinarians and other health professionals for comparative studies relevant to either human or animal medicine . The journal is open to subjects of common interest related to the immunology, immunopathology, microbiology, parasitology and epidemiology of human and animal infectious diseases, especially zoonotic infections, and animal models of human infectious diseases. The role of environmental factors in disease emergence is emphasized. CIMID is mainly focusing on applied veterinary and human medicine rather than on fundamental experimental research.
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