Swedish Museum of Natural History, Stockholm, Sweden.
PLoS One. 2007 Sep 12;2(9):e887. doi: 10.1371/journal.pone.0000887.
Analyses of the dynamics of diseases in wild populations typically assume all individuals to be identical. However, profound effects on the long-term impact on the host population can be expected if the disease has age and sex dependent dynamics. The Phocine Distemper Virus (PDV) caused two mass mortalities in European harbour seals in 1988 and in 2002. We show the mortality patterns were highly age specific on both occasions, where young of the year and adult (>4 yrs) animals suffered extremely high mortality, and sub-adult seals (1-3 yrs) of both sexes experienced low mortality. Consequently, genetic differences cannot have played a main role explaining why some seals survived and some did not in the study region, since parents had higher mortality levels than their progeny. Furthermore, there was a conspicuous absence of animals older than 14 years among the victims in 2002, which strongly indicates that the survivors from the previous disease outbreak in 1988 had acquired and maintained immunity to PDV. These specific mortality patterns imply that contact rates and susceptibility to the disease are strongly age and sex dependent variables, underlining the need for structured epidemic models for wildlife diseases. Detailed data can thus provide crucial information about a number of vital parameters such as functional herd immunity. One of many future challenges in understanding the epidemiology of the PDV and other wildlife diseases is to reveal how immune system responses differ among animals in different stages during their life cycle. The influence of such underlying mechanisms may also explain the limited evidence for abrupt disease thresholds in wild populations.
在对野生动物种群中的疾病动态进行分析时,通常假定所有个体都是相同的。然而,如果疾病具有年龄和性别依赖性动态,那么预计这将对宿主种群的长期影响产生深远的影响。犬瘟热病毒(PDV)在 1988 年和 2002 年导致欧洲港海豹发生了两次大规模死亡事件。我们表明,两次死亡模式都具有高度的年龄特异性,当年幼和成年(>4 岁)动物的死亡率极高,而亚成年海豹(1-3 岁)的死亡率则很低。因此,遗传差异不可能在研究区域中起到主要作用,解释为什么有些海豹存活而有些则没有,因为父母的死亡率高于其后代。此外,2002 年的死亡个体中明显没有年龄超过 14 岁的动物,这强烈表明,在 1988 年之前的疾病爆发中幸存下来的动物已经获得并维持了对 PDV 的免疫力。这些特定的死亡率模式意味着接触率和对疾病的易感性是强烈依赖年龄和性别的变量,这突出表明需要为野生动物疾病建立结构化的流行模型。详细的数据因此可以提供有关许多重要参数的关键信息,例如功能群体免疫。在理解 PDV 和其他野生动物疾病的流行病学方面,未来面临的众多挑战之一是揭示在其生命周期的不同阶段,动物的免疫系统反应如何存在差异。这些潜在机制的影响也可能解释了在野生种群中疾病阈值突然出现的证据有限的原因。