Evidence map›Paper›PMID 35062690›Full record

ArticleVaccines2021

Efficacy of the Newcastle Disease Virus Genotype VII.1.1-Matched Vaccines in Commercial Broilers.

Hesham A Sultan, Wael K Elfeil, Ahmed A Nour, Laila Tantawy, Elsayed G Kamel, Emad M Eed, Ahmad El Askary, Shaimaa Talaat

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 27 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Hesham A SultanDepartment of Birds and Rabbits Medicine, Faculty of Veterinary Medicine, University of Sadat City, Menoufiya 32958, Egypt.
Wael K ElfeilAvian and Rabbit Medicine Department, Faculty of Veterinary Medicine, Suez Canal University, Ismailia 51522, Egypt.ORCID 0000-0001-6777-982X
Ahmed A NourAgriculture Research Center, National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Giza 12566, Egypt.
Laila TantawyAgriculture Research Center, Pathology Department, Animal Health Research Institute, Giza 12566, Egypt.
Elsayed G KamelDepartment of Birds and Rabbits Medicine, Faculty of Veterinary Medicine, University of Sadat City, Menoufiya 32958, Egypt.
Emad M EedDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Ahmad El AskaryDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Shaimaa TalaatDepartment of Birds and Rabbits Medicine, Faculty of Veterinary Medicine, University of Sadat City, Menoufiya 32958, Egypt.
University of Sadat City · EGTaif University · SASuez Canal University · EG

Funding

Taif University Researchers Supporting Project TURSP-2020/157
6 · The paper itself

Abstract

Class II genotype VII Newcastle disease viruses (NDV) are predominant in the Middle East and Asia despite intensive vaccination programs using conventional live and inactivated NDV vaccines. In this study, the protective efficacies of three commercial vaccine regimes involving genotype II NDV, recombinant genotype VII NDV-matched, and an autogenous velogenic NDV genotype VII vaccine were evaluated against challenge with velogenic NDV genotype VII (accession number MG029120). Three vaccination regimes were applied as follows: group-1 received inactivated genotype II, group-2 received inactivated recombinant genotype VII NDV-matched, and group-3 received velogenic inactivated autogenous NDV genotype VII vaccines given on day 7; for the live vaccine doses, each group received the same live genotype II vaccine. The birds in all of the groups were challenged with NDV genotype VII, which was applied on day 28. Protection by the three regimes was evaluated after infection based on mortality rate, clinical signs, gross lesions, virus shedding, seroconversion, and microscopic changes. The results showed that these three vaccination regimes partially protected commercial broilers (73%, 86%, 97%, respectively, vs. 8.6% in non-vaccinated challenged and 0% in non-vaccinated non-challenged birds) against mortality at 10 days post-challenge (dpc). Using inactivated vaccines significantly reduced the virus shedding at the level of the number of shedders and the amount of virus that was shed in all vaccinated groups (G1-3) compared to in the non-vaccinated group (G-4). In conclusion, using closely genotype-matched vaccines (NDV-GVII) provided higher protection than using vaccines that were not closely genotype-matched and non-genotype-matched. The vaccine seeds that were closely related to genotype VII.1.1 provided higher protection against challenge against this genotype since it circulates in the Middle East region. Updating vaccine seeds with recent and closely related isolates provides higher protection.

Indexed as

commercial broilergenotype-matched vaccineinactivated vaccinematernal derived immunityNewcastle disease virus

Identifiers

PMID35062690
PMCPMC8779737
OpenAlexW4200285371

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.