Meiners C, Loesken S, Doehring S, Starick E, Pesch S, Maas A, Noe T, Beer M, Harder T, Grosse Beilage E
Prof. Dr. Elisabeth grosse Beilage, University of Veterinary Medicine Hannover, Field Station for Epidemiology, Buescheler Strasse 9, 49456 Bakum, Germany, Email:
Tierarztl Prax Ausg G Grosstiere Nutztiere. 2014;42(6):351-9. doi: 10.15653/TPG-131130. Epub 2014 Nov 18.
The aim of this field study was to explore the occurrence of and factors associated with the detection of swine influenza virus (SIV) by RTqPCR in weaner pigs and sows from herds with a history of respiratory or reproductive disorders.
The sample set was based on nasal swabs from 823 sows (123 submissions) and 562 weaner pigs (80 submissions). Nasal swab samples were taken and submitted by 51 veterinary practices from all over Germany. Corresponding to the pig density most of the submissions originated from the north-western part of Germany. The nasal swabs were used to detect SIV RNA by real-time RT-PCR (RTqPCR). Subtyping of SIV RNA by conventional RT-PCR and sequencing was attempted directly from clinical samples or from isolates when available. The herd characteristics, management and housing conditions of the pig herd as well as the course of the disease were collected by a telephone questionnaire with the herd attending veterinarian.
SIV was detected by RTqPCR in 53.8% of the submissions from weaner pigs with a history of respiratory disease. Moreover SIV was detected in 10.6% of the submissions from sows. The predominant endemic subtype found in nasal swabs from sows and weaner pigs was H1N1 (60.5%) whereas subtypes H1N2 (14.0%) and H3N2 (14.0%) were detected less frequently. In addition, human pandemic H1N1 virus or reassortants thereof were found in 11.5%.
The results underline the significance of a SIV infection in young pigs. A significant lower detection of SIV in wea- ner pigs was associated with the vaccination of piglets against por- cine circovirus type 2 (PCV2), possibly indicating an interaction of SIV and PCV2. Most of the positive samples from sows originated from gilts, whereas only two originated from sows. An association between reproductive disorders and the detection of SIV could not be confirmed.
本现场研究旨在探讨在有呼吸或繁殖障碍病史的猪群中,通过逆转录定量聚合酶链反应(RTqPCR)检测断奶仔猪和母猪中猪流感病毒(SIV)的情况及相关因素。
样本集基于来自823头母猪(123份送检样本)和562头断奶仔猪(80份送检样本)的鼻拭子。鼻拭子样本由德国各地的51家兽医诊所采集并送检。对应猪只密度,大部分送检样本来自德国西北部地区。鼻拭子用于通过实时逆转录聚合酶链反应(RTqPCR)检测SIV RNA。尝试直接从临床样本或可用的分离株中通过常规逆转录聚合酶链反应和测序对SIV RNA进行亚型鉴定。通过与猪群主治兽医的电话问卷调查收集猪群的群体特征、管理和饲养条件以及疾病病程。
在有呼吸道疾病病史的断奶仔猪的53.8%的送检样本中通过RTqPCR检测到SIV。此外,在母猪的10.6%的送检样本中检测到SIV。在母猪和断奶仔猪的鼻拭子中发现的主要地方流行亚型是H1N1(60.5%),而H1N2(14.0%)和H3N2(14.0%)亚型检测频率较低。此外,在11.5%的样本中发现了甲型H1N1流感大流行病毒或其重配体。
结果强调了SIV感染在仔猪中的重要性。断奶仔猪中SIV检测率显著较低与仔猪接种猪圆环病毒2型(PCV2)疫苗有关,这可能表明SIV与PCV2之间存在相互作用。母猪的大多数阳性样本来自后备母猪,而只有两份来自经产母猪。繁殖障碍与SIV检测之间的关联未得到证实。