Bovine endometrial cells do not mount an inflammatory response to Leptospira.

Reproduction & Fertility Pub Date : 2021-07-13 eCollection Date: 2021-07-01 DOI:10.1530/RAF-21-0012
Paula C C Molinari, Jarlath E Nally, John J Bromfield
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引用次数: 4

Abstract

Leptospirosis causes abortion, premature birth, and stillbirth in cattle, but the mechanisms remain unclear. Infected cattle shed Leptospira intermittently and present a range of clinical symptoms, making diagnosis difficult. The primary route of Leptospira transmission in any animal is the colonization of the renal tubule and excretion by urine; however, Leptospira can also colonize the female reproductive tract of cows and can be transmitted by semen. Vaccination against Leptospira in the US is routine in cattle, but immunity is not guaranteed. The cell wall of Leptospira contains toll-like receptor agonists including peptidoglycan and lipopolysaccharide. The capacity of Leptospira to initiate an innate inflammatory response from uterine endometrial cells is unknown but may be a cause of reproductive failure. Using cell culture, we tested the capacity of bovine endometrial epithelial cells or human monocytes to elicit an inflammatory response to Leptospira borgpetersenii serovar Hardjo strain TC273. Cells were exposed to either heat-killed Leptospira, Leptospira outer membrane, Escherichia coli lipopolysaccharide, Pam3CSK4 or medium alone for 2 to 24 h. Exposure of bovine endometrial epithelial cells or human monocytes to heat-killed Leptospira or Leptospira outer membrane did not induce the expression of IL1A, IL1B, IL6, or CXCL8, while exposure to E. coli lipopolysaccharide or Pam3CSK4 increased the expression of IL1A, IL1B, IL6, and CXCL8 compared to control cells. This data suggest that Leptospira does not trigger a classical inflammatory response in endometrial cells. Understanding the interaction between Leptospira and the female reproductive tract is important in determining the mechanisms of Leptospirosis associated with reproductive failure.

Lay summary: Cows infected with the Leptospira have abortion and stillbirth. It is not known how Leptospira causes pregnancy failure in the cow. We tested if Leptospira causes inflammation in cells of the uterus which triggers pregnancy failure. We collected cells from the uterus of healthy cows at the abattoir and placed them into culture with Leptospira and measured the expression of genes associated with inflammation. To our surprise, cells of the uterus did not respond to Leptospira; however, the same cells did respond to other disease-causing bacteria found in the uterus. This suggests that cells of the uterus can recognize bacteria and produce an inflammatory reaction but not in response to Leptospira. This finding suggests the immune system of the uterus cannot detect Leptospira which may go on to cause reproductive failure in cows. Understanding how Leptospira interact with cells of the uterus will help reduce pregnancy failure of cows with leptospirosis.

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牛子宫内膜细胞不会对钩端螺旋体产生炎症反应。
钩端螺旋体病导致牛流产、早产和死胎,但其机制尚不清楚。受感染的牛间歇性地传播钩端螺旋体,并表现出一系列临床症状,使诊断困难。钩端螺旋体在任何动物中传播的主要途径是在肾小管中定植并通过尿液排泄;然而,钩端螺旋体也可以在母牛的雌性生殖道中定居,并可以通过精液传播。在美国,对牛接种钩端螺旋体疫苗是常规做法,但不能保证免疫。钩端螺旋体细胞壁含有toll样受体激动剂,包括肽聚糖和脂多糖。钩端螺旋体引发子宫内膜细胞先天炎症反应的能力尚不清楚,但可能是生殖失败的原因之一。通过细胞培养,我们测试了牛子宫内膜上皮细胞或人单核细胞对博格彼得钩端螺旋体血清型Hardjo菌株TC273引起炎症反应的能力。将细胞分别暴露于热杀灭的钩端螺旋体、钩端螺旋体外膜、大肠杆菌脂多糖、Pam3CSK4或培养基中2 - 24小时。牛子宫内膜上皮细胞或人单核细胞暴露于热杀灭的钩端螺旋体或钩端螺旋体外膜中,不诱导IL1A、IL1B、IL6或CXCL8的表达,而暴露于大肠杆菌脂多糖或Pam3CSK4中,与对照细胞相比,IL1A、IL1B、IL6和CXCL8的表达增加。这些数据表明钩端螺旋体不会引发子宫内膜细胞的经典炎症反应。了解钩端螺旋体与女性生殖道之间的相互作用对于确定钩端螺旋体病与生殖衰竭相关的机制非常重要。摘要:感染钩端螺旋体的奶牛会流产和死产。目前尚不清楚钩端螺旋体是如何导致奶牛妊娠失败的。我们测试了钩端螺旋体是否会引起子宫细胞炎症,从而导致妊娠失败。我们从屠宰场的健康奶牛的子宫中收集细胞,并将其与钩端螺旋体一起培养,并测量与炎症相关的基因表达。令我们惊讶的是,子宫细胞对钩端螺旋体没有反应;然而,同样的细胞确实对子宫内发现的其他致病细菌有反应。这表明子宫细胞可以识别细菌并产生炎症反应,但对钩端螺旋体没有反应。这一发现表明子宫的免疫系统无法检测到钩端螺旋体,而钩端螺旋体可能会导致奶牛的繁殖失败。了解钩端螺旋体如何与子宫细胞相互作用将有助于减少患钩端螺旋体病奶牛的妊娠失败。
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