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233 protocols using floqswab

1

Healthy Adult Carriage of S. mitis

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A prospective pilot carriage study was conducted among healthy adults in November 2019 to obtain S. mitis isolates that would test the robustness and discriminatory power of the developed genomic tools. Healthy adults above the age of 18 who were UCL students or staff were eligible. Current or recent antibiotic use within 2 weeks prior to sampling was an exclusion criterion. In total, 12 healthy adults were recruited.
Briefly, nasopharyngeal, oral, and oropharyngeal samples were obtained. Nasopharyngeal swab samples were taken with Copan FLOQswabs (Copan, USA) using a previously described technique (45 (link)). Oral swab samples were taken using Copan FLOQswabs, and to ensure adequate sampling of regions known to be colonized by S. mitis (12 (link)), the surface of the teeth, dorsum of the tongue, hard palate, left and right buccal mucosa, and maxillary and mandibular gingiva were sampled with the same swab. Both oral and nasopharyngeal swabs were stored in skim milk-tryptone-glucose-glycerol (STGG) medium. Cough samples were obtained from volunteers directly onto sterile Columbia blood agar (CBA) plates. Additional respiratory samples were collected using a facemask device with a soluble polyvinyl alcohol (PVA) inner strip as previously described (46 (link)), and PVA strips were dissolved in Todd-Hewitt broth with yeast extract (THY) culture medium prior to inoculation.
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2

Nasopharyngeal Sample Collection and SARS-CoV-2 Testing

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Two nasopharyngeal samples were obtained from each patient for further testing: one with a sponge swab™ (NIPRO, Osaka, Japan) for antigen testing, and the other with FLOQSwab™ (Copan Italia S.p.A., Brescia, Italy) for the RT-PCR assay. After sample collection, antigen testing was performed immediately using the QuickChaser® Auto SARS-CoV-2 and QuickChaser Immuno Reader II. FLOQSwab samples were diluted in 3 mL of Universal Transport Medium™ (UTM™) (Copan Italia) for in-house RT-PCR and reference RT-PCR.
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3

Specimen Collection Methods for HPV Testing

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Cervical samples were collected using an L-shaped FLOQSwab® (Copan, Brescia, Italy) and transported in a tube with 20 mL of PreservCyt® Solution (HOLOGIC, Marlborough, MA, USA). All samples were well shaken using vortex for 30 seconds, and 1.5 mL aliquots were made.
Vaginal self-samples were obtained using a FLOQSwab® (Copan, Brescia, Italy) and transported dry to the laboratory. Each specimen was suspended in 5.5 mL of PreservCyt® Solution (HOLOGIC, Marlborough, MA, USA), and 5 aliquots were made.
The Colli-Pee® 20 mL device allowed for capturing a first-void urine volume of 13 mL (+/− 2 mL), in a collection device containing 7 mL of preservative urine conservation medium (UCM), leading to a final volume of 20 mL (+/− 2 mL) [15 (link)]. Urine samples were aliquoted after arrival at the laboratory. One aliquot of each type of sample was sent to the Division of Laboratory Medicine of the European Institute of Oncology, Milan, Italy, for HPV testing.
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4

Placental Tissue Sampling for Microbiome

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Swabs (FLOQSwabs; COPAN, Murrieta, CA, USA) for molecular microbiology were collected from the chorioamniotic membranes, the amnion-chorion interface of the placental disc, and the placental villous tree. These swabs were stored at −80°C until DNA extractions were performed.
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5

Obesity-associated Gastric Microbiome Profiling

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In total, 24 samples were obtained from 14 individuals undergoing sleeve gastrectomy for morbid obesity at Ersta Hospital in Stockholm, Sweden. Samples were processed within 40 minutes. The BIOHIT H. pylori quick-test kit (Biohit HealthCare) was used to detect infection in 2 representative pieces of fundus and antrum. HPI status was confirmed by culturing swab samples from 28 to 32 gastric sites on GC agar plates (Karolinska Hospital, catalog MIK0346) under microaerophilic condition. Characteristics of the participants, based on questionnaire data, are listed in Supplemental Table 1.
Epithelial microbiome samples were collected from fundus and antrum using swabs (FLOQSwabs, Copan Flock Technologies), and stored in DNA/RNA shield (Zymo Research) at –80°C until DNA extraction and metagenome sequencing. Fundus and antrum tissues were processed for isolation of mononuclear cells. Antrum and fundus tissues (approximately 1 cm2) were snap-frozen for immunofluorescence microscopy.
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6

Vaginal Microflora Collection and Analysis

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Example 63

The vaginal microflora were collected in duplicate from the left and right sides of the vaginal sidewall using FLOQSwabs® (Copan Diagnostics, USA) (Jacobson J., et al. 2014. Vaginal microbiome changes with levonorgestrel intrauterine system placement. Contraception. 90(2): 130-135). To control for variables that can alter the vaginal microbiome, samples were collected at the same time of a woman's menstrual cycle (i.e., one week into the menstrual cycle) and patients were tested for pregnancy and for recent sexual activity (using a prostate-specific antigen membrane test).

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7

Increasing Cervical Cancer Screening

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The control arm corresponds to women receive a conventional invitation letter sent by post to the home address of eligible women recommending them to make an appointment to a doctor or a midwife for the collection of a cervical specimen. The two experimental interventions are: 1) eligible women receive at their home address a vaginal self-sampling kit (FLOQSwabs® Copan Diagnostics, Brescia, Italy) in addition to the conventional invitation letter; and 2) eligible women receive at their home address a urine collection kit (Colli-Pee device, Novosanis, Wijnegem, Belgium) in addition to the conventional invitation letter.
With the conventional invitation letter, the women will receive an information brochure on the study (arms 2 and 3), a questionnaire (half of the population of the three arms), a self-sampling device with instruction (arms 2 and 3) and a prepaid return envelope. The women who will receive the self-sampling kit will place their prepaid return envelope in a post box.
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8

Buccal Swabs for Infant DNA

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A buccal swab (FLOQSwabs, Copan) is rubbed on the inside of the infant’s cheeks, stored at − 20 °C until genomic DNA isolation for genotyping studies.
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9

Comprehensive Surveillance of C. auris

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Known C. auris carriers were cultured for C. auris and bacterial multidrug-resistant organisms (MDROs) at the bilateral nares, axillae, inguinal creases, palms/fingertips, and perianal skin. Samples were collected immediately before room disinfection. Flocked swabs (FLOQSwabs, Copan, Murrieta, CA) were used to sample a 5 × 5 cm2 area from each body site, then placed in Amies transport medium with neutralizer.
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10

Respiratory Pathobionts Cohort Protocol

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The Respiratory Pathobionts cohort, a subset of participants screened for eligibility for the CORTIS-01 trial at the Worcester site, has previously been described24 (link). Briefly, HIV-uninfected participants were consecutively enroled in this sub-study irrespective of CORTIS-01 enrolment, or signs and symptoms of upper respiratory tract infections. Paired nasopharyngeal and oropharyngeal flocked swabs (FLOQSwabs, Copan Diagnostics, Murrieta, CA, USA) were collected and stored in Primestore buffer (Longhorn Vaccines and Diagnostics, San Antonio, TX, USA) at −80 °C, and viral and bacterial nucleic acid was later extracted (Qiasymphony Virus/Bacteria Mini Kit, Qiagen, Hilden, Germany) and quantified using a multiplex RT-qPCR assay kit (Respiratory Pathogens 33 Kit, Fast Track Diagnostics, Luxembourg) on the CFX96 Touch System lightcycler platform (Bio-Rad, Hercules, CA, USA), according to the manufacturer’s instructions. Participants co-enroled into the CORTIS-01 trial were investigated for TB at baseline; those only enroled into the Respiratory Pathobionts cohort were not investigated for TB (Supplementary Fig. S1c). All participants provided written, informed consent and the protocols were approved by the University of Cape Town Faculty of Health Sciences Human Research Ethics Committee (HREC 327/2017).
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