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{"title":"Pregnancy-related listeriosis","authors":"Rahat Wadhwa Desai, Mary Alice Smith","doi":"10.1002/bdr2.1012","DOIUrl":null,"url":null,"abstract":"<div>\n <p>About one in seven cases of listeriosis occurs in pregnant women, and, although listeriosis is rare, it is the third leading cause of death from food-borne infections. Pregnancy-related listeriosis increases the risk for fetal and neonatal mortality by approximately 21%. During pregnancy, infections are more likely to occur in the third trimester (66%) than the first trimester (3%). However, fetal and neonatal adverse effects are less common as gestational age increases or with older gestational age at birth. Pregnant women seem highly susceptible in some listeriosis outbreaks making up a large percentage of cases, whereas others contain very few. Whether this results from differences in strains of <i>L. monocytogenes</i>, exposures, or other factors remains to be determined. Food and Agriculture Organization of United Nations/World Health Organization (FAO/WHO) estimates the human lethal dose for 50% (LD<sub>50</sub>) for fetal/neonatal loss is 1.9 × 10<sup>6</sup> colony forming units (CFUs) <i>L. monocytogenes</i>. Animal models have been developed for pregnancy-related listeriosis showing similar susceptibility and clinical outcomes as in humans. Nonhuman primate and guinea pig animal models have similar (LD<sub>50</sub>) values to the estimated human LD<sub>50</sub>. Additional animal studies are needed to understand the pathways leading to fetal and neonatal listeriosis in humans. More information is needed to understand dose response, to model risk for listeriosis at lower concentrations, and to determine why some pregnant women may be more susceptible than others. To better treat listeriosis during pregnancy, biomarkers for early diagnosis of listeriosis are also needed. Last, pregnant women need to be educated about avoiding high-risk foods, like Mexican-style cheese and ready-to-eat meats. Birth Defects Research 109:324–335, 2017.© 2017 Wiley Periodicals, Inc.</p>\n </div>","PeriodicalId":9121,"journal":{"name":"Birth Defects Research","volume":"109 5","pages":"324-335"},"PeriodicalIF":1.6000,"publicationDate":"2017-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/bdr2.1012","citationCount":"44","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Birth Defects Research","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bdr2.1012","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 44
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Abstract
About one in seven cases of listeriosis occurs in pregnant women, and, although listeriosis is rare, it is the third leading cause of death from food-borne infections. Pregnancy-related listeriosis increases the risk for fetal and neonatal mortality by approximately 21%. During pregnancy, infections are more likely to occur in the third trimester (66%) than the first trimester (3%). However, fetal and neonatal adverse effects are less common as gestational age increases or with older gestational age at birth. Pregnant women seem highly susceptible in some listeriosis outbreaks making up a large percentage of cases, whereas others contain very few. Whether this results from differences in strains of L. monocytogenes , exposures, or other factors remains to be determined. Food and Agriculture Organization of United Nations/World Health Organization (FAO/WHO) estimates the human lethal dose for 50% (LD50 ) for fetal/neonatal loss is 1.9 × 106 colony forming units (CFUs) L. monocytogenes . Animal models have been developed for pregnancy-related listeriosis showing similar susceptibility and clinical outcomes as in humans. Nonhuman primate and guinea pig animal models have similar (LD50 ) values to the estimated human LD50 . Additional animal studies are needed to understand the pathways leading to fetal and neonatal listeriosis in humans. More information is needed to understand dose response, to model risk for listeriosis at lower concentrations, and to determine why some pregnant women may be more susceptible than others. To better treat listeriosis during pregnancy, biomarkers for early diagnosis of listeriosis are also needed. Last, pregnant women need to be educated about avoiding high-risk foods, like Mexican-style cheese and ready-to-eat meats. Birth Defects Research 109:324–335, 2017.© 2017 Wiley Periodicals, Inc.
妊娠相关李氏杆菌病
大约七分之一的李斯特菌病发生在孕妇身上,虽然李斯特菌病很罕见,但它是食源性感染导致死亡的第三大原因。妊娠相关的李斯特菌病使胎儿和新生儿死亡的风险增加约21%。在怀孕期间,感染更可能发生在妊娠晚期(66%),而不是妊娠早期(3%)。然而,随着胎龄的增加或出生时胎龄的增大,胎儿和新生儿的不良反应不太常见。孕妇在一些李斯特菌病暴发中似乎非常易感,占病例的很大比例,而在其他病例中则很少。这是否由于单核细胞增生乳杆菌菌株的差异,暴露或其他因素仍有待确定。联合国粮食及农业组织/世界卫生组织(FAO/WHO)估计,50% (LD50)胎儿/新生儿损失的人类致死剂量为1.9 × 106菌落形成单位(cfu)单增乳杆菌。已经开发了与妊娠相关的李斯特菌病的动物模型,显示出与人类相似的易感性和临床结果。非人灵长类动物和豚鼠动物模型的LD50值与估计的人类LD50值相似。需要进一步的动物研究来了解导致人类胎儿和新生儿李斯特菌病的途径。需要更多的信息来了解剂量反应,模拟较低浓度下李斯特菌病的风险,并确定为什么一些孕妇可能比其他孕妇更容易感染。为了更好地治疗妊娠期李斯特菌病,还需要用于李斯特菌病早期诊断的生物标志物。最后,孕妇需要接受有关避免高风险食物的教育,如墨西哥式奶酪和即食肉类。出生缺陷研究[j], 2017。©2017 Wiley期刊公司
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