人类创造的环境对巴西野生新热带灵长类动物葡萄球菌致病性和耐药性的影响。

IF 2 3区 农林科学 Q4 IMMUNOLOGY
Indiara Sales , Olney Vieira-da-Motta , Ana Tavares , Carlos Ramón Ruiz-Miranda , Hermínia de Lencastre , Maria Miragaia
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引用次数: 0

摘要

非人灵长类动物(non-human primate, NHP)罗马狮子(Leontopithecus rosalia)是巴西本土的一种濒危物种,生活在与人类有不同程度接触(自然、私人和城市)的森林碎片中。其他NHPs (Callithrix spp)是由人类引入的,并与这些森林中的本地物种共存并相互作用。为了评估生活在人类改造环境中或接近人类改造环境是否会构成罗莎利亚葡萄球菌的风险,我们比较了从不同森林片段中收集的本地和引进种葡萄球菌的流行率、遗传背景、抗生素敏感性和毒力基因含量。我们发现,在人类主导的环境中,玫瑰乳杆菌与哺乳球菌(原人类葡萄球菌)的定殖率从18%增加到85% (p = 0.0001), Callithrix spp与金黄色葡萄球菌的定殖率从6%增加到100% (p = 0.0001)。根据分子分型数据获得的差异可能是由于这些细菌物种从入侵的NHP物种和人类传播。随着暴露于人类环境的增加,潘通-瓦伦丁白介素基因的流行率和对-内酰胺类、大环内酯类和/或林肯胺类药物的耐药性的增加与微生物群的变化是平行的。特别是,来自Callithrix spp.的金黄色葡萄球菌对红霉素的耐药率从0%上升到50%,而来自rosalia L.凝固酶阴性葡萄球菌对至少一种抗生素的耐药率从13%上升到56% (p = 0.0003)。我们的研究结果表明,本地动物物种与人类创造的环境接触增加了共生菌群中抗菌素耐药菌和致病菌的含量,最终会影响它们的健康。重要性:濒危动物物种易受环境变化的影响,人类活动已多次被确定为导致自然景观剧烈变化的因素。监测受保护物种周围环境的变化是极其重要的,因为这可能导致早期发现任何潜在的威胁。在这项研究中,我们发现L. rosalia(一种来自巴西的受保护的非人灵长类动物)与人类环境的接触与它们的共生微生物群的变化有关。其中包括致病性和耐抗生素细菌数量的增加,这些细菌更有可能引起更难治疗的感染。我们提供了人类接触对罗莎莉娅菌有害影响的证据。此外,我们的研究结果表明,监测受保护动物物种的共生微生物群可能是感知受保护物种对人类暴露风险的有用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of human created environments in the pathogenic potential and antimicrobial resistance of staphylococci from wild neotropical primates in Brazil

The non-human primate (NHP) Leontopithecus rosalia is an endangered species native of Brazil and lives in forest fragments with different levels of contact with humans (natural, private and urban). Other NHPs – Callithrix spp. - were introduced by humans and co-exist and interact with the native species in these forests.

To evaluate if living in or close to human-modified environments could constitute a risk for L. rosalia, we compared the prevalence, genetic background, antibiotic susceptibility and virulence gene content of staphylococci collected from the native and the introduced species from different forest fragments.

We found that presence in human-dominated environments increased the colonization rate of L. rosalia with Mammaliicoccus sciuri (former Staphylococcus sciuri) from 18 % to 85 % (p = 0.0001) and of Callithrix spp with Staphylococcus aureus from 6 % to 100 % (p = 0.0001). According to molecular typing data obtained differences probably resulted from dissemination of these bacterial species from the invader NHP species and from humans. Changes in microbiota were paralleled by an increase in the prevalence of Panton-Valentine Leukocidin gene and in resistance to beta-lactams, macrolides and/or lincosamides as exposure to human environment increased. In particular, erythromycin resistance in S. aureus from Callithrix spp. increased from 0 % to 50 % and resistance rate to at least one antibiotic in coagulase-negative staphylococci species from L. rosalia increased from 13 % to 56 % (p = 0.0003).

Our results showed that contact of native animal species with human-created environments increased the content of antimicrobial resistant and pathogenic bacteria on their commensal microbiota, which ultimately can impact on their health.

Importance

Endangered animal species are vulnerable to environmental alterations and human activities have been repeatedly identified as factors driving drastic changes in the natural landscape. It is extremely important to monitor changes in the environment surrounding protected species, because this could lead to early detection of any potential threats. In this study, we found that the contact of L. rosalia - a protected non-human primate from Brazil - with human environments is related to changes in their commensal microbiota. These included an increase in the number of pathogenic and antibiotic resistant bacteria, which have a higher potential to cause infections that are more difficult to treat. We provided evidence for the harmful impact human contact has on L. rosalia. Also, our results suggest that monitoring of commensal microbiota of protected animal species might be a useful way of sensing the risks of protected species to human exposure.

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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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