Warner Alan J, Tokach Mike D, Carrender Brittany, Amachawadi Raghavendra G, Labbé Alain, Heuser Walter, Coble Kyle, DeRouchey Joel M, Woodworth Jason C, Goodband Robert D, Kalam Ramya, Shi Xiaorong, Nagaraja T G, Gebhardt Jordan T
Department of Animal Sciences and Industry, College of Agriculture, Kansas State University, Manhattan, KS 66506-0201, USA.
JBS Live Pork, LLC, Greeley, CO 65101, USA.
Transl Anim Sci. 2023 Aug 1;7(1):txad093. doi: 10.1093/tas/txad093. eCollection 2023.
A total of 34,749 pigs were used in two experiments to evaluate the effects of a postbiotic dried fermentation product () administered through drinking water on nursery pig growth performance, antibiotic injection frequency, morbidity, mortality, fecal consistency, and characterization of fecal . The DFP is composed of bioactive molecules derived from In Exp. 1, 350 barrows (DNA Line 200 × 400; initial body weight [] 6.1 ± 0.01 kg) were used in a 42-d study with five pigs per pen and 35 pens per treatment. The DFP was supplied for 14 d at a target dosage of 24 mg/kg BW using a water medicator at a 1:128 dilution. On days 7 and 14, fecal samples were collected for dry matter () and to determine, by a multiplex polymerase chain reaction () assay, prevalence of 11 virulence genes characteristic of . pathotypes. There was no evidence ( > 0.10) for differences for growth, incidence of diarrhea, number of antibiotic injections, removals, or fecal DM. On both fecal collection days, . virulence genes were present with day 7 samples positive for genes that encode for hemolysins (, , intimin (, and enteroaggregative heat-stable enterotoxin (. Prevalence of enterotoxin genes (, ) increased on day 14, but DFP had no effects on the prevalence of any of the virulence genes. A total of 32 out of 72 . isolates were identified as enterotoxigenic pathotype and all except one were from day 14 fecal samples. Fourteen isolates were positive for F4 fimbria and one isolate was positive for F4 and F18 fimbriae. In Exp. 2, 34,399 nursery pigs (initially 5.6 kg) were used in 20 nursery barns with 10 barns per treatment (control or DFP). The target dosage of the DFP for the first 14 d was 35 mg/kg BW. Following the 14-d supplementation period, pigs continued to be monitored for approximately 31 d. There was no evidence ( > 0.05) for the DFP to influence the overall percentage of pigs that died or growth performance. From days 0 to 14, providing the DFP reduced ( < 0.05) the percentage of pigs that were euthanized. However, providing the DFP increased ( < 0.05) the overall percentage of pigs that were euthanized and total mortality. For the number of antibiotic injections (treatment interventions), providing the DFP reduced the number of injections for the common period ( < 0.001) and overall ( = 0.002). These results indicate that the DFP did not influence growth performance but providing the DFP in Exp. 2 led to increased total nursery pig mortality.
在两项实验中,共使用了34749头猪来评估通过饮水给予后生元干发酵产品(DFP)对保育猪生长性能、抗生素注射频率、发病率、死亡率、粪便稠度以及粪便微生物特征的影响。DFP由源自[具体来源未提及]的生物活性分子组成。在实验1中,选用了350头公猪(DNA品系200×400;初始体重[IBW]6.1±0.01千克)进行为期42天的研究,每栏饲养5头猪,每个处理设置35个栏位。使用加药器以1:128的稀释度,按照24毫克/千克体重的目标剂量提供DFP,持续14天。在第7天和第14天,采集粪便样本测定干物质(DM)含量,并通过多重聚合酶链反应(mPCR)检测11种[具体病原体未提及]致病型特征毒力基因的流行情况。在生长、腹泻发生率、抗生素注射次数、淘汰率或粪便干物质方面,没有证据表明存在差异(P>0.10)。在两个粪便采集日,均检测到[具体病原体未提及]毒力基因,第7天的样本中编码溶血素(hlyA、hlyF)、紧密黏附素(eaeA)和肠集聚耐热肠毒素(EAST1)的基因呈阳性。肠毒素基因(elt、est)的流行率在第14天有所增加,但DFP对任何毒力基因的流行率均无影响。在72株[具体病原体未提及]分离株中,共有32株被鉴定为产肠毒素致病型,除1株外均来自第14天的粪便样本。14株分离株F4菌毛呈阳性,1株分离株F4和F18菌毛均呈阳性。在实验2中,34399头保育猪(初始体重5.6千克)被用于20个保育栏舍,每个处理10个栏舍(对照或DFP)。DFP在前14天的目标剂量为35毫克/千克体重。在14天的补充期后,继续对猪进行约31天的监测。没有证据表明DFP会影响死亡猪的总体百分比或生长性能(P>0.05)。在第0天至第14天,提供DFP可降低(P<0.05)实施安乐死的猪的百分比。然而,提供DFP会增加(P<0.05)实施安乐死的猪的总体百分比和总死亡率。对于抗生素注射次数(治疗干预),提供DFP可减少共同期(P<0.001)和总体(P=0.002)的注射次数。这些结果表明,DFP不影响生长性能,但在实验2中提供DFP会导致保育猪总死亡率增加。