- Research note
- Open Access
Air sampling for detection of infectious laryngotracheitis (ILT) in commercial poultry flocks
BMC Research Notes volume 13, Article number: 556 (2020)
Infectious laryngotracheitis (ILT) is an acute and highly contagious viral respiratory disease of poultry, caused by gallid herpesvirus 1 (ILTV), which causes significant economic losses. Due to recent outbreaks of ILT in Australia, it has been proposed that ILT could be transmitted between poultry sheds by airborne transmission; however, there has never been direct detection of ILTV from air samples. We aimed to optimize a sampling system for the detection of airborne ILTV in poultry sheds.
Poultry farms with a known outbreaks of ILT were used for detection of airborne ILTV. Infected chickens were verified by detection of ILTV nucleic acid in feather shafts with all farms being positive. Using a liquid cyclonic impinging device, it was found that recovery and detection of airborne ILTV was possible in alkaline PEG buffer. Additional sampling was performed at different heights to determine the presence of ILTV in the air. In farm 3, all three air samples at both heights were positive for ILTV while at farm 2 only one sample at 45 cm was positive. We envisaged in the future air sampling will be able to detect and track potential transmission of ILTV both inside and outside of the poultry shed.
The causative agent of infectious laryngotracheitis (ILT) is gallid herpesvirus 1, a highly contiguous virus that is characterized by severe dyspnea, coughing, and rales . ILT infection has a significant economic impact on the poultry industry across the world due to reduce egg production and large mortality rate (up to 70%) . Live attenuated vaccines, and biosecurity measures are currently the most effective control measures for ILT . However, outbreaks of ILT occur regularly in Australia and recently, this resulted in novel strains due to recombination of the vaccine strains [3, 4].
Due to the substantial increase in the number of outbreaks of ILT in broiler farms in the Mornington Peninsula area of Victoria raised the concerns about the route of transmission of gallid herpesvirus 1. Potential sources of gallid herpesvirus 1 infection between poultry farms are infected chickens, contaminated litter, dust, drinking water, fomites and darkling beetles, which infect poultry through ocular and respiratory routes . However, there were concerns that transmission between farms were occurring by being air. A single report suggests that airborne transmission is the likelihood of infection is ten times higher when within the vicinity of a clinically infected farm and within the vicinity of market gardens that apply raw poultry manure as fertiliser however, no direct testing of air was performed . It has also been shown that relatively high levels of infectious gallid herpesvirus 1 are carried in dust which could result in increased airborne transmission . Some other viral poultry diseases are transmitted by air, and thus it is a priority to determine if the wind also spreads gallid herpesvirus 1. Here, we report a sampling system for the detection of airborne gallid herpesvirus 1 in commercial poultry sheds.
Materials and methods
Farm identification, selection and definitions
In this study, three case farms were selected throughout March and April of 2017 from a list of broiler farms located in the Mornington Peninsula region, Victoria. The flocks were comprised of mixed-sex of Cobb and Ross broiler breeds between 36–50 days of age. Upon the onset of an outbreak of ILT in a poultry farm based on clinical diagnosis, the company veterinarian or service person notified the investigators. As soon as ILT case farms had been identified, an investigator visited the farm and collected air samples within 24 h.
Air sampling procedure
All air samples were collected using the SKC Biosampler®; a liquid cyclonic impinging device (SKC Inc, USA) and BioLite pump (SKC Inc, USA) as shown in Fig. 1. Briefly, the collection vessel contained 5 ml of alkaline polyethene glycol (PEG) solution (60% v/v PEG 200 (Sigma-Aldrich, USA), 20 mM KOH, pH 13.5) or phosphate buffer saline (PBS) (8.1 mM Na2HPO4, 137 mM NaCl, 1.4 mM KH2HPO4 and 2.6 mM KCl) in which material from the air was trapped. The air sampler was used for 20 min in three different locations within the shed at the height of either 45 cm or 120 cm off the floor at a rate of 12.5 L per min placed on card table. In between sampling, the glass collection vessel was disinfected with 80% ethanol. Each sample was transferred from the collection vessel to a clean sterile 15 ml conical centrifuge tubes for transport and storage in the laboratory at –20 °C.
DNA extraction of feather samples
Feather samples were gathered randomly off the floor inside the selected sampling shed. Feathers were collected and stored in 50 ml conical centrifuge tubes and stored at –20 °C until processing. Approximately 5 mm of each collected feather shaft was cut off and were divided into groups of three, with four shafts per group. Total DNA was extracted from feathers tips using the Mouse Direct PCR Kit (Biotool, USA) following the manufacturer’s instructions.
DNA purification of air and feather samples
DNA purification from air and feather samples were performed as described by Li and Sheen with the following modifications . Briefly, 500 μl of DNA binding solution (6 M NaI) is added to 300 μl of extracted DNA feather sample to which 10 μl of 100 mg/ml silica dioxide (Sigma, USA) was added, vortexed then incubated at room temperature for 2 min. Samples were centrifuged for 10 s, and the supernatant removed. Silica matrix was then washed with 500 μl of washing solution (50% v/v ethanol, 10 mM Tris–HCl pH 7.5, 100 mM NaCl and 1 mM ethylenediaminetetraacetic acid (EDTA), centrifuged at 13,000xg, discarded supernatant and repeated once. Silica matrix was resuspended in 30 μl of sterile water and incubated at 70 °C for 2 min. The samples were centrifuged at 16,000xg for 2 min and eluted DNA transferred to a fresh tube and stored at −20 °C. A similar purification method was used for the air sample except the starting volume was 2.5 ml to which 3 ml of DNA binding solution and 100 μl of 100 mg/ml silica dioxide (Sigma, USA) was added. DNA was eluted by the addition of 100 μl of sterile water.
PCR for detection of Gallid herpesvirus 1
Conventional PCR was used for the detection of gallid herpesvirus 1 by the presence of the thymidine kinase (TK) gene, as described by Mahmoudian et al. (2011), with the following modifications . Reactions were carried out in a final volume of 25 µL and amplified in a C-Master GT thermal cycler (Dynamica, Australia). The following amplification conditions consisted of an initial denaturation step of 94 °C for 3 min, 94 °C for 15 s, 60 °C for 45 s, 72 °C for 150 s, repeated for 35 times with a final extension at 72 °C for 3 min. Amplicon size was checked by agarose electrophoresis migration by loading directly on 1% (w/v) agarose (Lonza, USA) gel, prepared as per manufacturer’s instructions, with the addition of 0.5 µL of Sybr® Safe DNA Gel Stain (Life Technologies, USA). The gel was run at 110 V for 45 min and imaged using the GelDocTM XR + (BioRad, USA) instrument and software.
Air samples in farm 1 were initially collected using a PBS buffer; however, the presence of gallid herpesvirus 1 was not detected suggesting the possibility this buffer is unsuitable for collection of viral samples (Fig. 2) (Additional file 1). However, the use of alkaline PEG as a collection buffer in farms 2 and 3 allowed the detection of gallid herpesvirus 1 by amplification of the TK gene (2250 bp amplicon) on new farms (Fig. 2). Sampling occurred at two heights with all sample sites and heights in farm 3 being positive for gallid herpesvirus 1 while only one site in farm 2 at 45 cm off the floor was positive (Fig. 2). All farms that were sampled had reported outbreaks of ILT and thus to confirm the presence of ILTV infected chickens on farms; a non-invasive method was used . Feathers were collected off the ground and DNA extracted from shafts. The presence of gallid herpesvirus 1 was seen at all farms with Farm 3 showing the highest level of infection (Fig. 3) (Additional file 1).
We have developed a sampling system for the detection of airborne gallid herpesvirus 1 by PCR. The initial use of PBS buffer to collect airborne material was unsuccessful which was a surprise as has been used in the past as a collection media in the successful isolation of airborne Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) and influenza H1N1 [10, 11]. However, this was done in conjunction with other solutions such as ethylene glycol, bovine serum albumin (BSA) and activated charcoal . The use of alkaline PEG solution as sample buffer was successful in detecting the presence of gallid herpesvirus 1 which may be due to the fact this solution causes lysis of majority of microbes and inhibition of enzymes due to high pH which would preserve nucleic acid . However, the use of this buffer excludes testing whether the detected nucleic acid was infectious. On farm 3 both measured heights 45 cm and 120 cm recorded positive samples in comparison with farm 2, which only had one positive sample at 45 cm high. This is approximately the same level as a chicken’s mouth. It has been shown that relative humidity (RH) can affect the airborne transmission of influenza virus, as demonstrated in the guinea pig model with deficient transmission at mid-range and very high RH . Ideally the RH should be between 50 and 70% in poultry shed (https://www.poultryventilation.com/node/4925) however the RH in each shed at farms 2 and 3 was not directly measured it was observed that on day of collection farm 2 had high humidity (> 70%). In contrast, on farm 3 it had low humidity (< 50%) suggesting that the humidity could be another factor that affects the transmission of gallid herpesvirus 1 by air.
To confirm the presence of gallid herpesvirus 1 on farms, feather shafts were used as a source of our DNA. This method is particularly beneficial as they are easy to collect, non-lethal for the bird, therefore useful for monitoring purposes. The majority of feather samples were positive for the presence of gallid herpesvirus 1, except for one sample in farm 2. On farm 2 it appears to have a low level of infection which may be why only one of the air samples from this farm returned a positive result.
In the future, this method will allow us to investigate whether transmission of ILT between poultry farms could occur via the air. In addition, these results will enable greater insight into the use of air sampling for the detection of other poultry viral diseases. This information will help in the deployment of air sampling and feather collection as means for a non-invasive biosecurity surveillance for the poultry industry.
There are several limitations of this current study. (1) The current use of alkaline PEG does not allow for isolation and viability testing of the collected virus; thus use of PBS is required. Further work is required to develop a collection buffer to allow isolation and viability testing of gallid herpesvirus 1. (2) It appears humidity can play a role in the ability of gallid herpesvirus 1 to be airborne and direct measurements of humidity in sheds are required. (3) There were no molecular tests performed to distinguish the collected gallid herpesvirus 1 virus from vaccine strains and field isolates in this study. (4) The need to use quantitative PCR (qPCR) to measure v.
Availability of data and materials
The information supporting the conclusions of this article is included in the article.
Gallid herpesvirus 1
Polymerase chain reaction
Phosphate buffer saline
Porcine Reproductive and Respiratory Syndrome Virus
Fuchs W, Veits J, Helferich D, Granzow H, Teifke JP, Mettenleiter TC. Molecular biology of avian infectious laryngotracheitis virus. Vet Res. 2007;38(2):261–79.
Ou SC, Giambrone JJ. Infectious laryngotracheitis virus in chickens. World J Virol. 2012;1(5):142–9.
Blacker HP, Kirkpatrick NC, Rubite A, O’Rourke D, Noormohammadi AH. Epidemiology of recent outbreaks of infectious laryngotracheitis in poultry in Australia. Aust Vet J. 2011;89(3):89–94.
Lee SW, Markham PF, Coppo MJ, Legione AR, Markham JF, Noormohammadi AH, Browning GF, Ficorilli N, Hartley CA, Devlin JM. Attenuated vaccines can recombine to form virulent field viruses. Science. 2012;337(6091):188.
Johnson YJ, Gedamu N, Colby MM, Myint MS, Steele SE, Salem M. NL T: wind-Borne Transmission of Infectious Laryngotracheitis Between Commercial Poultry Operations. Int J Poultry Sci. 2005;4:263–7.
Roy P, Fakhrul Islam AFM, Burgess SK, Hunt PW, McNally J, Walkden-Brown SW. Real-time PCR quantification of infectious laryngotracheitis virus in chicken tissues, faeces, isolator-dust and bedding material over 28 days following infection reveals high levels in faeces and dust. J Gen Virol. 2015;96(11):3338–47.
Li JF, Sheen J. DNA purification from multiple sources in plant research with homemade silica resins. Methods Mol Biol. 2012;862:53–9.
Mahmoudian A, Kirkpatrick NC, Coppo M, Lee SW, Devlin JM, Markham PF, Browning GF, Noormohammadi AH. Development of a SYBR Green quantitative polymerase chain reaction assay for rapid detection and quantification of infectious laryngotracheitis virus. Avian Pathol. 2011;40(3):237–42.
Davidson I, Raibshtein I, Altori A, Elkin N. Infectious laryngotracheitis virus (ILTV) vaccine intake evaluation by detection of virus amplification in feather pulps of vaccinated chickens. Vaccine. 2016;34(13):1630–3.
Fabian P, McDevitt JJ, Houseman EA, Milton DK. Airborne influenza virus detection with four aerosol samplers using molecular and infectivity assays: considerations for a new infectious virus aerosol sampler. Indoor Air. 2009;19(5):433–41.
Hermann JR, Hoff SJ, Yoon KJ, Burkhardt AC, Evans RB. Zimmerman JJOptimizationon of a sampling system for recovery and detection of airborne porcine reproductive and respiratory syndrome virus and swine influenza virus. Appl Environ Microbiol. 2006;72(7):4811–8.
Chomczynski P, Rymaszewski M: Alkaline polyethylene glycol-based method for direct PCR from bacteria, eukaryotic tissue samples, and whole blood. Biotechniques 2006, 40(4):454, 456, 458.
Lowen AC, Mubareka S, Steel J, Palese P. Influenza virus transmission is dependent on relative humidity and temperature. PLoS Pathog. 2007;3(10):1470–6.
We would like to thank the participating poultry owners for their time and assistance during sample collection.
Funding was granted for this project from Rural Industries Research and Development Corporation (RIRDC) and La Trobe University RFA industry collaboration grant. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Ethics approval and consent to participate
Consent for publication
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Brown, L., Premaratna, D., Segal, Y. et al. Air sampling for detection of infectious laryngotracheitis (ILT) in commercial poultry flocks. BMC Res Notes 13, 556 (2020). https://doi.org/10.1186/s13104-020-05399-2
- Air sampling
- Gallid herpesvirus 1