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A BSTRACT
Respiratory infections of sheep and goats cause heavy morbidity and mortality, leading to huge economic losses. Conventional methods
of diagnosis that include isolation and identifcation of incriminating microbes are time-consuming and fraught with logistic challenges.
Direct detection of incriminating microbes using molecular tools is gaining popularity in clinical, microbiological settings. In this study,
a total of 50 samples (44 nasal swabs and 6 lung tissues) from sheep and goats were screened for the detection of diferent bacterial
species by in vitro amplifcation of genus or species-specifc genes. Histophilus somni was detected in 2% goat samples, Trueperella
pyogenes in 20% goat nasal swabs, whereas 22% goat nasal swab samples were found positive for Mycoplasma spp. None of the samples
from sheep was detected positive for H. somni, T. pyogenes, Mycoplasma spp. Similarly, all samples, irrespective, whether from sheep or
goats, showed negative results for Pasteurella multocida, Mannheimia haemolytica, and Corynebacterium pseudotuberculosis.
Keywords: Goat, Histophilus somni, Mycoplasma, Respiratory infections, Sheep, Trueperella pyogenes.
Ind J of Vet Sci and Biotech (2019): 10.21887/ijvsbt.15.2.6
Molecular Detection of Bacterial Pathogens Directly from the
Nasal Swabs and Lung Tissue of Sheep and Goats
Sunaina Thakur
1
, Subhash Verma
2
*, Prasenjit Dhar
3
, Mandeep Sharma
4
I NTRODUCTION
I
nfectious diseases are a common cause of economic losses
to small ruminants, mainly sheep and goat husbandry. To
enable sheep and goat husbandry viable and sustainable
amongst rural people, the development and use of
techniques for early and accurate diagnosis hold prime
importance (Chakraborty et al., 2014). Respiratory diseases
of small ruminants are multifactorial (Lacasta et al., 2008),
and there are multiple etiological agents responsible
for the respiratory disease complex. The most common
bacterial causes of respiratory infections are P. multocida,
Mannheimia hemolytica, Mycoplasma spp., Corynebacterium
pseudotuberculosis, Histophilus somni, and Trueperella
pyogenes. These bacteria are commonly found in the
respiratory tract of sheep and goats and induce morbidity
and mortality under immunosuppressive conditions.
Mycoplasma infections cause indirect economic losses as a
result of emaciation, delayed market weight, and infertility,
owing to the sub-acute or chronic pneumonia, especially
in small ruminants, which are of great importance in rural
development. A major health problem of small ruminants
is pneumonia/ pleuropneumonia, which may be caused
by Mycoplasma species alone or in conjunction with other
microbes (Adehan et al., 2006). The isolation of these bacterial
species is time-consuming and requires diferent media and
laboratory conditions. The objective of this study was to
fll up the gap in the literature in the detection of bacterial
pathogens directly from the nasal swabs and lung tissue of
sheep and goats through PCR technology.
RESEARCH ARTICLE
1-4
Department of Veterinary Microbiology, DGCN College
of Veterinary Science and Animal Husbandry, CSKHPKV,
Palampur-176062 (HP), India
Corresponding Author: Subhash Verma, Department of
Veterinary Microbiology, DGCN College of Veterinary Science and
Animal Husbandry, CSKHPKV, Palampur-176062 (HP), India, e-mail:
sverma8@gmail.com
How to cite this article: Thakur, S., Verma, S., Dhar, P. and Sharma,
M. (2019). Molecular Detection of Bacterial Pathogens Directly
from the Nasal Swabs and Lung Tissue of Sheep and Goats. Ind J
Vet Sci and Biotech, 15(2): 22-25.
Source of support: Nil
Confict of interest: None.
Submitted: 25/08/2019 Accepted: 10/09/2019 Published: 25/11/2019
M ATERIALS AND METHODS
Sampling and Transportation
A total of 50 samples comprising of 44 nasal swabs from 15
sheep and 29 goats; and 6 lung tissues from 2 sheep and 4
goats having respiratory disease symptoms (nasal discharge,
sneezing, coughing, and respiratory distress) were collected
in PBS and transported on ice to the laboratory. All samples
were stored at 4ºC until processed.
Molecular Detection through In Vitro Amplifcation
All samples were processed for DNA extraction as per the
Phenol Chloroform Isoamyl alcohol (PCI) protocol given by
Sambrook et al. (1989). The polymerase chain reaction was
performed for the detection of diferent bacterial species