Evaluation of a new diagnostic method for quantification of EBV and HHV-6 viral load in bronchoalveolar lavage

2019 ◽  
Vol 31 (3) ◽  
Author(s):  
Jessica Montemezzo ◽  
Filippo Patrucco ◽  
Francesco Gavelli ◽  
Linda Ferrari ◽  
Giulia Faolotto ◽  
...  
2020 ◽  
Vol 58 (7) ◽  
pp. 958-964
Author(s):  
Wataru Shibata ◽  
Mamiko Niki ◽  
Kanako Sato ◽  
Hiroki Fujimoto ◽  
Koichi Yamada ◽  
...  

Abstract Mucormycosis is a deep-seated fungal infection that mainly develops in patients with severe immunodeficiencies such as those with malignant hematological diseases. Despite poor prognosis, there is no reliable and minimally invasive diagnostic method—such as serodiagnosis—for making a clinical decision regarding the condition. As early diagnosis and early treatment improve the prognosis of mucormycosis, the development of a sensitive early diagnostic method is important. We had previously identified a Rhizopus-specific antigen (RSA) by signal sequence trapping and retrovirus-mediated expression (SST-REX), and evaluated its utility as a diagnostic antigen by constructing a sandwich enzyme-linked immunosorbent assay (ELISA) system to detect serum RSA levels in inoculated mice. In this study, we used the RSA-specific rabbit monoclonal antibodies generated by novel hybridoma technology to improve the sensitivity of the ELISA system. We observed an increase in serum and bronchoalveolar lavage fluid (BALF) levels of RSA in mouse model 1 day after inoculation, suggesting that this newly developed monoclonal antibody-based ELISA system may be useful for the diagnosis of mucormycosis in the early stages of infection. In addition, we measured RSA levels in human serum and BALF, and found that serum RSA level was higher in mucormycosis patients (15.1 ng/ml) than that in invasive pulmonary aspergillosis patients (0.53 ng/ml) and the negative control (0.49 ng/ml). Our results suggest that RSA may be a powerful tool for the diagnosis of pulmonary mucormycosis, and its differentiation from other deep-seated mycoses such as aspergillosis.


2021 ◽  
Author(s):  
Neeltje van Doremalen ◽  
Jyothi N. Purushotham ◽  
Jonathan E. Schulz ◽  
Myndi G. Holbrook ◽  
Trenton Bushmaker ◽  
...  

AbstractIntramuscular vaccination with ChAdOx1 nCoV-19/AZD1222 protected rhesus macaques against pneumonia but did not reduce shedding of SARS-CoV-2. Here we investigate whether intranasally administered ChAdOx1 nCoV-19 reduces shedding, using a SARS-CoV-2 virus with the D614G mutation in the spike protein. Viral load in swabs obtained from intranasally vaccinated hamsters was significantly decreased compared to controls and no viral RNA or infectious virus was found in lung tissue, both in a direct challenge and a transmission model. Intranasal vaccination of rhesus macaques resulted in reduced shedding and a reduction in viral load in bronchoalveolar lavage and lower respiratory tract tissue. In conclusion, intranasal vaccination reduced shedding in two different SARS-CoV-2 animal models, justifying further investigation as a potential vaccination route for COVID-19 vaccines.


2006 ◽  
Vol 36 ◽  
pp. S9 ◽  
Author(s):  
C.F.M. Linssen ◽  
J.A. Jacobs ◽  
F. Stelma ◽  
W.N.K.A. van Mook ◽  
M. Drent ◽  
...  

2020 ◽  
Author(s):  
Sandeep Chakraborty

‘Nipah virus is a biosafety level 4 (BSL-4) pathogen that causes severe respiratory illness and encephalitis in humans’ [1] that orginates in bats [2]. It was first isolated in Malaysia and Singapore in 1999 - ‘late September 1998 and by mid-June 1999, more than 265 encephalitis cases, including 105 deaths, had been reported in Malaysia, and 11 cases of encephalitis or respiratory illness with one death had been reported in Singapore’ [3]. It keeps recurring in Bangladesh [4]. There was a 2018 outbreak in Kerala, India [5]. There seems to have been a simultaneous outbreak in Wuhan during Covid19 - which never got reported, and apparently resolved by itself.Metagenome from the bronchoalveolar lavage fluid of 5 Covid19 [6–8] patients from Wuhan (Accid:PRJNA605983) which showed very little SAR-Cov2 viral load (in the tens per million reads) in my analysis earlier [9].The metagenome also shows the co-infection with Nipah henipavirus virus in 4 out of 5 patients. The sequences are in SI:Nipah.fa - 167 reads in all.One can almost assemble the full genome (about 18kbps) from it. It seems to have originated from Bangladesh, though I have not done the phylogeny. Most reads are 100% identical, but some are (97% - 145/150).Maybe, we have looking for the wrong virus in the rest of the world - since Nipah is endemic to Southeast Asia, which seems to have been the least affected in Covid19.


1999 ◽  
Vol 159 (5) ◽  
pp. 1439-1444 ◽  
Author(s):  
HOMER L. TWIGG ◽  
DIAA M. SOLIMAN ◽  
RICHARD B. DAY ◽  
KENNETH S. KNOX ◽  
RODNEY J. ANDERSON ◽  
...  

2021 ◽  
Vol 13 (12) ◽  
Author(s):  
Zahra Eslamirad ◽  
Abdolatif Moini ◽  
Mojtaba Didehdar ◽  
Reza Hajihossein ◽  
Ali Arash Anoushiravani

Background: Protozoa have the ability to replace the human lung. Over recent years, the incidence of pulmonary infections caused by these microorganisms has increased, particularly in individuals with an immunodeficiency. The use of appropriate diagnostic methods is particularly important in the identification of parasites in pulmonary secretions. Objectives: The present study aimed to evaluate and compare PCR-based diagnostic methods with the gold standard method to detect three pathogenic protozoa, including Toxoplasma, Cryptosporidium, and Microsporidia in bronchoalveolar lavage (BAL) samples obtained from immunocompromised patients with chronic obstructive pulmonary disease. Methods: A BAL sample of immunodeficient patients suffering from chronic obstructive pulmonary disease (COPD) was examined by direct microscopy and PCR methods. Results: In this study, we examined 64 patients with immunodeficiency accompanied by COPD. Microsporidia were not identified in the samples. Direct methods identified three and nine cases of Toxoplasma and Cryptosporidium, respectively. However, the molecular method identified two and two cases of pulmonary infection with these parasites. Conclusions: Determining the standard diagnostic method for parasites is dependent on factors, such as the type of specimen and the type of parasite. Based on the results of the present study, the direct microscopic method is the optimal diagnostic method for Toxoplasma and Cryptosporidium in BAL samples.


2015 ◽  
Vol 2 (suppl_1) ◽  
Author(s):  
Isabelle Paula Lodding ◽  
Hans Henrik Schultz ◽  
Jens Ulrik Jensen ◽  
Claus Andersen ◽  
Michael Perch ◽  
...  

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